diff --git "a/demonstrations/dfmvlxx/dom_snapshots/page-28-0.json" "b/demonstrations/dfmvlxx/dom_snapshots/page-28-0.json"
new file mode 100644--- /dev/null
+++ "b/demonstrations/dfmvlxx/dom_snapshots/page-28-0.json"
@@ -0,0 +1 @@
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"2e889fb9-cb9d-4b07", "", "M448 1536h896v-256h-896v256zm0-640h896v-384h-160q-40 0-68-28t-28-68v-160h-640v640zm1152 64q0-26-19-45t-45-19-45 19-19 45 19 45 45 19 45-19 19-45zm128 0v416q0 13-9.5 22.5t-22.5 9.5h-224v160q0 40-28 68t-68 28h-960q-40 0-68-28t-28-68v-160h-224q-13 0-22.5-9.5t-9.5-22.5v-416q0-79 56.5-135.5t135.5-56.5h64v-544q0-40 28-68t68-28h672q40 0 88 20t76 48l152 152q28 28 48 76t20 88v256h64q79 0 135.5 56.5t56.5 135.5z", "9a39bc03-b41b-481d", "", "doccontentwrapper collapse show", "collapseExample0", "82d6d40c-f09b-4943", "", "article-content-ad", "5a6c22eb-86f9-42ef", "", "AdThrive_Header_1_desktop", "adthrive-ad adthrive-header adthrive-header-1 adthrive-ad-cls", "min-height: 90px;", "data-google-query-id", "CN-mwdqG_P8CFXCVrAIdEQ0PAg", "dcba37a7-066b-4079", "", "google_ads_iframe_/18190176,21678768125/AdThrive_Header_1/5dc336ff22eddf534ab4417c_0__container__", "border: 0pt none; display: inline-block; width: 300px; height: 250px;", "59b030e8-1dee-42a5", "", "frameborder", "0", "https://7094b0a42ea257b84b542bb4e74a3f95.safeframe.googlesyndication.com/safeframe/1-0-40/html/container.html", "google_ads_iframe_/18190176,21678768125/AdThrive_Header_1/5dc336ff22eddf534ab4417c_0", "3rd party ad content", "scrolling", "no", "marginwidth", "marginheight", "300", "250", "data-is-safeframe", "sandbox", "allow-forms allow-popups allow-popups-to-escape-sandbox allow-same-origin allow-scripts allow-top-navigation-by-user-activation", "region", "aria-label", "Advertisement", "data-google-container-id", "7", "border: 0px; vertical-align: bottom;", "data-load-complete", "f9b2499f-f927-444f", "", "7a5130fe-7284-4e08", "", "ORGANIC CHEMISTRY", "H2", "04a831b9-2c46-42da", "", "CONCEPT", "a9c48a5e-10f9-44c4", "", "There was once a time when chemists thought \"organic\" referred only to things that were living, and that life was the result of a spiritual \"life force.\" While there is nothing wrong with viewing life as having a spiritual component, spiritual matters are simply outside the realm of science, and to mix up the two is as silly as using mathematics to explain love (or vice versa). In fact, the \"life force\" has a name: carbon, the common denominator in all living things. Not everything that has carbon is living, nor are all the areas studied in ", "interlinked", "c405e65c-46ad-4cb1", "", "font-family:Lucida Sans Unicode;", "38d2bebe-89e9-48f3", "", "\u2014", "the branch of chemistry devoted to the study of carbon and its compounds", "a0528b31-8e42-4deb", "", "always concerned with living things. Organic chemistry addresses an array of subjects as vast as the number of possible compounds that can be made by strings of carbon atoms. We can thank ", "a86ac66a-82ba-421e", "", " for much of what makes life easier in the modern age: fuel for cars, for instance, or the plastics found in many of the products used in an average day.", "9a676dea-9b49-43bd", "", "HOW IT WORKS", "H3", "b979412d-027f-4962", "", "Introduction to Carbon", "bfcd86cd-ea66-4d22", "", "As the element essential to all of life, and hence the basis for a vast field of study, carbon is addressed in its own essay. The Carbon essay, in addition to examining the chemical properties of carbon (discussed below), approaches a number of subjects, such as the allotropes of carbon. These include three crystalline forms (graphite, diamond, and buckminsterfullerene), as well as amorphous carbon. In addition, two oxides of carbon", "c7b40a80-b5a5-4a68", "", "/science-and-technology/chemistry/compounds-and-elements/carbon-dioxide", "1f4b40bb-5e98-456b", "", "carbon dioxide", " and ", "/science-and-technology/chemistry/compounds-and-elements/carbon-monoxide", "64ca6ede-44d6-41cf", "", "carbon monoxide", "0d8a9119-3b2f-48c8", "", "are important, in the case of the former, to the natural ", "/science-and-technology/biology-and-genetics/biology-general/carbon-cycle", "5392fdbb-2caa-46da", "", "carbon cycle", ", and in the case of the latter, to industry. Both also pose environmental dangers.", "7900e927-8bc8-473a", "", "The purpose of this summary of the carbon essay is to provide a hint of the complexities involved with this sixth element on the ", "/science-and-technology/chemistry/chemistry-general/periodic-table", "72ddab1f-fd08-46bb", "", "periodic table", ", the 14th most abundant element on ", "data-topic", "1207885", "/earth-and-environment/geology-and-oceanography/geology-and-oceanography/earth", "a0a2e4fd-cbd5-497b", "", "Earth", ". In the human body, carbon is second only to oxygen in abundance, and accounts for 18% of the body's mass. Capable of combining in seemingly endless ways, carbon, along with hydrogen, is at the center of huge families of compounds. These are the hydrocarbons, present in deposits of fossil fuels: ", "/science-and-technology/chemistry/organic-chemistry/natural-gas", "867ba02f-5844-4e33", "", "natural gas", ", petroleum, and coal.", "H4", "f551e05b-1d12-4b6d", "", "A PROPENSITY FOR LIMITLESS BONDING.", "ef5cfb0c-adf2-49cf", "", "Carbon has a valence electron configuration of 2s", "SUP", "517451d9-22a2-4034", "", "2", "2p", "9b8e09f1-4c21-4770", "", ". Likewise all the members of Group 4 on the ", "c14660fa-f97b-4f00", "", " (Group 14 in the IUPAC version of the table)", "bb536d31-77f6-4bd2", "", "sometimes known as the \"carbon family\"", "7612aced-e6e4-4fa1", "", "have configurations of ns", "6369c194-1cd5-499b", "", "np", "e9f0994b-0a52-48e4", "", ", where n is the number of the period or row the element occupies on the table. There are two elements noted for their ability to form long strings of atoms and seemingly endless varieties of molecules: one is carbon, and the other is silicon, directly below it on the periodic table.", "41d1242a-715e-4298", "", "Just as carbon is at the center of a vast network of organic compounds, silicon holds the same function in the inorganic realm. It is found in virtually all types of rocks, except the calcium carbonates", "3f4cbaf3-a48f-4a38", "", "which, as their name implies, contain carbon. In terms of known elemental mass, silicon is second only to oxygen in abundance on Earth. Silicon atoms are about one and a half times as large as those of carbon; thus not even silicon can compete with carbon's ability to form\nan almost limitless array of molecules in various shapes and sizes, and with various chemical properties.", "AdThrive_Content_1_desktop", "adthrive-ad adthrive-content adthrive-content-1 adthrive-ad-cls", "min-height: 250px;", "CKGDx9mG_P8CFfIC1Qod4pkPgw", "e0edbb09-cdf6-4cf8", "", "google_ads_iframe_/18190176,21678768125/AdThrive_Content_1/5dc336ff22eddf534ab4417c_0__container__", "border: 0pt none; display: inline-block; width: 728px; height: 90px;", "4e120906-7dd0-4441", "", "google_ads_iframe_/18190176,21678768125/AdThrive_Content_1/5dc336ff22eddf534ab4417c_0", "728", "90", "6", "1057d698-9876-4a10", "", "98a87c5f-fb9f-4371", "", "Electronegativity", "a24b4f95-8bef-499a", "", "Carbon is further distinguished by its high value of electronegativity, the relative ability of an atom to attract valence electrons. To mention a few basic aspects of chemical bonding, developed at considerably greater length in the Chemical Bonding essay, if two atoms have an electric charge and thus are ions, they form strong ionic bonds. Ionic bonding occurs when a metal bonds with a nonmetal. The other principal type of bond is a ", "/science-and-technology/chemistry/chemistry-general/covalent-bond", "5ae27276-a69a-4e1b", "", "covalent bond", ", in which two uncharged atoms share eight valence electrons. If the electronegativity values of the two elements involved are equal, then they share the electrons equally; but if one element has a higher electronegativity value, the electrons will be more drawn to that element.", "622d0a32-15c6-4992", "", "The electronegativity of carbon is certainly not the highest on the periodic table. That distinction belongs to fluorine, with an electronegativity value of 4.0, which makes it the most reactive of all elements. Fluorine is at the head of Group 7, the halogens, all of which are highly reactive and most of which have high electronegativity values. If one ignores the noble gases, which are virtually unreactive and occupy the extreme right-hand side of the periodic table, electronegativity values are highest in the upper right-hand side of the table", "f8730ba5-3bdf-40bf", "", "the location of fluorine", "763d7c57-3f74-4d42", "", "and lowest in the lower left. In other words, the value increases with group or column number (again, leaving out the noble gases in Group 8), and decreases with period or row number.", "AdThrive_Content_2_desktop", "adthrive-ad adthrive-content adthrive-content-2 adthrive-ad-cls", "CKLmwtmG_P8CFVkQ1QodDRwNqA", "328f715f-27f4-4a9b", "", "google_ads_iframe_/18190176,21678768125/AdThrive_Content_2/5dc336ff22eddf534ab4417c_0__container__", "22a67cf7-d437-4d2b", "", "google_ads_iframe_/18190176,21678768125/AdThrive_Content_2/5dc336ff22eddf534ab4417c_0", "5", "21819ca4-32cb-4b16", "", "cb334a62-ddee-451f", "", "With an electronegativity of 2.5, carbon ties with sulfur and iodine (a halogen) for sixth place, behind only fluorine; oxygen (3.5); nitrogen and chlorine (3.0); and bromine (2.8). Thus its electronegativity is high, without being too high. Fluorine is not likely to form the long chains for which is carbon is known, simply because its electronegativity is so high, it overpowers other elements with which it comes into contact. In addition, with four valence electrons, carbon is ideally suited to find other elements (or other carbon atoms) for forming covalent bonds according to the octet rule, whereby most elements bond so that they have eight valence electrons.", "bab5bf23-0fcf-45d2", "", "Carbon's Multiple Bonds", "4f278787-5407-4e56", "", "Carbon", "0213685a-ebbd-4032", "", "with its four valence electrons", "d7ce6d4d-e2a1-452b", "", "happens to be tetravalent, or capable of bonding to four other atoms at once. It is not necessarily the case that an element has the ability to bond with as many other elements as it has valence electrons; in fact, this is rarely the case. Additionally, carbon is capable of forming not only a single bond, with one pair of shared valence electrons, but a double bond (two pairs) or even a triple bond (three pairs.)", "c5fa944d-6562-49de", "", "Another special property of carbon is its ability to bond in long chains that constitute strings of carbons and other atoms. Furthermore, though sometimes carbon forms a typical molecule (for example, ", "8ab762ba-1aab-4d11", "", ", or CO", "SUB", "8e46ce89-e76d-4e4f", "", "2,", " is just one carbon atom with two oxygens), it is also capable of forming \"molecules\" that are really not molecules in the way that the word is typically used in chemistry. Graphite, for instance, is just a series of \"sheets\" of carbon atoms bonded tightly in a hexagonal, or six-sided, pattern, while a diamond is simply a huge \"molecule\" composed of carbon atoms strung together by covalent bonds.", "AdThrive_Content_3_desktop", "adthrive-ad adthrive-content adthrive-content-3 adthrive-ad-cls", "eb039b77-7ee5-4a36", "", "google_ads_iframe_/18190176,21678768125/AdThrive_Content_3/5dc336ff22eddf534ab4417c_0__container__", "border: 0pt none; display: inline-block;", "cb584bec-4ab7-42d6", "", "ec757eea-66d0-4706", "", "78efe640-0cb3-46a5", "", "Organic chemistry is the study of carbon, its compounds, and their properties. The only major carbon compounds considered inorganic are carbonates (for instance, ", "/science-and-technology/chemistry/compounds-and-elements/calcium-carbonate", "77f19ce0-7472-44a8", "", "calcium carbonate", ", alluded to above, which is one of the major forms of mineral on Earth) and oxides, such as carbon dioxide and ", "0e033986-8a53-4641", "", ". This leaves a huge array of compounds to be studied, as we shall see.", "e101d7b4-c76c-4dfe", "", "The term \"organic\" in everyday language connotes \"living,\" but organic chemistry is involved with plenty of compounds not part of living organisms: petroleum, for instance, is an organic compound that ultimately comes from the decayed bodies of organisms that once were alive. It should be stressed that organic compounds do not have to be produced by living things, or even by things that once were alive; they can be produced artificially in a laboratory.", "f8f40567-7cd6-4ccb", "", "The breakthrough event in organic chemistry came in 1828, when German chemist Friedrich W", "4648fb99-d135-4511", "", "\u00f6", "hler (1800-1882) heated a sample of ammonium cyanate (NH", "ee1244eb-7616-465b", "", "4", "OCN) and converted it to urea (H", "7ecc4da7-195c-48bb", "", "N-CO-NH", "ae2f706f-c6f8-4adb", "", "). Ammonium cyanite is an inorganic material, whereas urea, a waste product in the urine of mammals, is an organic one. \"Without benefit of a kidney, a bladder, or a\ndog,\" as W", "ba85ce19-8bf8-4888", "", "hler later said, he had managed to transform an inorganic substance into an organic one.", "AdThrive_Content_4_desktop", "adthrive-ad adthrive-content adthrive-content-4 adthrive-ad-cls", "5a538ffb-cea6-4f63", "", "60bb4734-9662-484b", "", "Ammonium cyanate and urea are isomers: substances having the same formula, but possessing different chemical properties. Thus they have exactly the same numbers and proportions of atoms, yet these atoms are arranged in different ways. In urea, the carbon forms an organic chain, and in ammonium cyanate, it does not. Thus, to reduce the specifics of organic chemistry even further, this discipline can be said to constitute the study of carbon chains, and ways to rearrange them to create new substances.", "c550d5ee-8970-4bd1", "", "REAL-LIFE APPLICATIONS", "7ab9a878-1d75-4ffe", "", "Organic Chemistry and Modern Life", "c0efce71-9164-4790", "", "At first glance, the term \"organic chemistry\" might sound like something removed from\neveryday life, but this could not be further from the truth. The reality of the role played by organic chemistry in modern existence is summed up in a famous advertising slogan used by E. I. du Pont de Nemours and Company (usually referred to as \"du Pont\"): \"Better Things for Better Living Through Chemistry.\"", "3fd1ecc3-a357-43f0", "", "Often rendered simply as \"Better Living Through Chemistry,\" the advertising campaign made its debut in 1938, just as du Pont introduced a revolutionary product of organic chemistry: nylon, the creation of a brilliant young chemist named Wallace Carothers (1896-1937). Nylon, an example of a polymer (discussed below), started a revolution in plastics that was still unfolding three decades later, in 1967. That was the year of the film ", "74fc4fdb-8eb3-4514", "", "The Graduate", ", which included a famous interchange between the character of Benjamin Braddock (", "/people/literature-and-arts/film-and-television-biographies/dustin-hoffman", "cd5fccb4-a29f-4515", "", "Dustin Hoffman", ") and an adult named Mr. McGuire (Walter Brooke):", "AdThrive_Content_5_desktop", "adthrive-ad adthrive-content adthrive-content-5 adthrive-ad-cls", "c7d0d9f9-14ec-448d", "", "41ac6a5a-35cd-4eeb", "", "cf7a1e15-2a0e-44fb", "", " Mr. McGuire: I just want to say one word to you", "476b87c4-eb3c-4fa7", "", "\u2026", " just one word.", "01e8c9f3-6ecc-46f6", "", " Benjamin Braddock: Yes, sir.", "7c7293f8-b731-4855", "", " Mr. McGuire: Are you listening?", "b6dbdfcf-c71a-47a6", "", " Benjamin Braddock: Yes, sir, I am.", "d2486e3f-6b00-4b8e", "", " Mr. McGuire: Plastics.", "d0bd189a-fafa-4e73", "", "The meaning of this interchange was that plastics were the wave of the future, and that an intelligent young man such as Ben should invest his energies in this promising new field. Instead, Ben puts his attention into other things, quite removed from \"plastics,\" and much of the plot revolves around his revolt against what he perceives as the \"plastic\" (that is, artificial) character of modern life.", "fcb2cc35-2822-4c2c", "", "In this way, ", "28755e9c-0545-4c4e", "", " spoke for a whole generation that had become ambivalent concerning \"better living through chemistry,\" a phrase that eventually was perceived as ironic in view of concerns about the environment and the many artificial products that make up modern life. Responding to this ambivalence, du Pont dropped the slogan in the late 1970s; yet the reality is that people truly do enjoy \"better living through chemistry\"", "204f0e04-1d7b-436c", "", "particularly organic chemistry.", "AdThrive_Content_6_desktop", "adthrive-ad adthrive-content adthrive-content-6 adthrive-ad-cls", "ee2580fe-9157-4980", "", "2b6ecebf-a44b-4ac4", "", "APPLICATIONS OF ORGANIC CHEMISTRY.", "10215ecc-1e18-4697", "", "What would the world be like without the fruits of organic chemistry? First, it would be necessary to take away all the various forms of rubber, vitamins, cloth, and paper made from organically based compounds. Aspirins and all types of other drugs; preservatives that keep food from spoiling; perfumes and toiletries; dyes\nand flavorings", "e470580b-5d17-44fd", "", "all these things would have to go as well.", "b6833b54-0719-4999", "", "/science-and-technology/chemistry/chemistry-general/synthetic-fibers", "c140f97e-4ec5-4a9b", "", "Synthetic fibers", " such as nylon", "e40c0446-cc46-4e8d", "", "used in everything from toothbrushes to parachutes", "8a2ae41d-9a97-4f87", "", "would be out of the picture if it were not for the enormous progress made by organic chemistry. The same is true of plastics or polymers in general, which have literally hundreds upon hundreds of applications. Indeed, it is virtually impossible for a person in twenty-first century America to spend an entire day without coming into contact with at least one, and more likely dozens, of plastic products. Car parts, toys, computer housings, Velcro fasteners, PVC (", "/science-and-technology/chemistry/organic-chemistry/polyvinyl-chloride", "fd9a4280-e915-4561", "", "polyvinyl chloride", ") plumbing pipes, and many more fixtures of modern life are all made possible by plastics and polymers.", "96cea5c5-6ea4-4552", "", "Then there is the vast array of petrochemicals that power modern civilization. Best-known among these is gasoline, but there is also coal, still one of the most significant fuels used in electrical power plants, as well as ", "4a39f740-2c3c-48d1", "", " and various other forms of oil used either directly or indirectly in providing heat, light, and electric power to homes. But the influence of petrochemicals extends far beyond their applications for fuel. For instance, the roofing materials and tar that (quite literally) keep a roof over people's heads, protecting them from sun and rain, are the product of petrochemicals", "e21837b0-61e6-4517", "", "and ultimately, of organic chemistry.", "AdThrive_Content_7_desktop", "adthrive-ad adthrive-content adthrive-content-7 adthrive-ad-cls", "35c2dfd0-30c8-4af9", "", "b8ee777f-82f6-4d6a", "", "Hydrocarbons", "ca6e8e52-bc6d-482d", "", "Carbon, together with other elements, forms so many millions of organic compounds that even introductory textbooks on organic chemistry consist of many hundreds of pages. Fortunately, it is possible to classify broad groupings of organic compounds. The largest and most significant is that class of organic compounds known as hydrocarbons", "6661ceb9-985c-4d3f", "", "chemical compounds whose molecules are made up of nothing but carbon and hydrogen atoms.", "2025a752-30ef-4bcf", "", "Every molecule in a hydrocarbon is built upon a \"skeleton\" composed of carbon atoms, either in closed rings or in long chains. The chains may be straight or branched, but in each case", "d62b39f2-3acb-4cee", "", "rings or chains, straight chains or branched ones", "4272e9d3-b1bd-4e45", "", "the carbon bonds not used in tying the carbon atoms together are taken up by hydrogen atoms.", "5fd3da6d-3160-42df", "", "Theoretically, there is no limit to the number of possible hydrocarbons. Not only does carbon form itself into apparently limitless molecular shapes, but hydrogen is a particularly good partner. It has the smallest atom of any element on the periodic table, and therefore it can bond to one of carbon's valence electrons without getting in the way of the other three.", "AdThrive_Content_8_desktop", "adthrive-ad adthrive-content adthrive-content-8 adthrive-ad-cls", "9d023978-3952-4065", "", "3092df2a-bdaf-49cd", "", "There are two basic varieties of hydrocarbon, distinguished by shape: aliphatic and aromatic. The first of these forms straight or branched chains, as well as rings, while the second forms only benzene rings, discussed below. Within the aliphatic hydrocarbons are three varieties: those that form single bonds (alkanes), double bonds (alkenes), and triple bonds (alkynes.)", "be1a6ac2-d51f-4567", "", "ALKANES.", "de3bfec9-8cc1-4cac", "", "The alkanes are also known as saturated hydrocarbons, because all the bonds not used to make the skeleton itself are filled to their capacity (that is, saturated) with hydrogen atoms. The formula for any alkane is C", "c8e5e360-7c9c-45fd", "", "n", "H", "d132b692-276c-48ad", "", "2n+2", ", where n is the number of carbon atoms. In the case of a linear, unbranched alkane, every carbon atom has two hydrogen atoms attached, but the two end carbon atoms each have an extra hydrogen.", "7c54d1f1-83b0-4286", "", "What follows are the names and formulas for the first eight normal, or unbranched, alkanes. Note that the first four of these received common names before their structures were known; from C", "b80cc5c8-5c04-477b", "", " onward, however, they were given names with Greek roots indicating the number of carbon atoms (e.g., octane, a reference to \"eight.\")", "AdThrive_Content_9_desktop", "adthrive-ad adthrive-content adthrive-content-9 adthrive-ad-cls", "90acccf8-66a7-4a2d", "", "84c504d1-fd7f-4488", "", "cd9c4f98-7c34-4475", "", " Methane (CH", "23fc4089-7dcd-4d9f", "", ")", "8935fc16-ff6d-4730", "", " Ethane (C", "5933c09a-71a3-4792", "", "49d0078c-aa7a-4671", "", "4fd3a35c-5a28-45c3", "", " Propane (C", "1ad8926e-019f-4a00", "", "3", "b0829129-1695-4dc9", "", "8", "1f6710a9-8743-42fe", "", " Butane (C", "f7af979d-6bb9-4019", "", "25611cf2-5181-44d9", "", "10", "5188569e-e4b2-4e3f", "", " Pentane (C", "95cdeb76-4aa6-4222", "", "15a4a0c8-dbff-4277", "", "12", "cf532cad-c598-45d9", "", " Hexane (C", "8ad15159-7d30-4d0b", "", "d87100c4-22ca-40e4", "", "7a44d454-52ae-4700", "", " Heptane (C", "78f5745d-ed58-4eb4", "", "a60c0876-6eed-4ae8", "", "16", "2853f4bd-267b-47da", "", " Octane (C", "e691eee1-e455-4d9a", "", "175838e1-f838-4737", "", "18", "49244357-b154-4c0f", "", "The reader will undoubtedly notice a number of familiar names on this list. The first four, being the lowest in molecular mass, are gases at room temperature, while the heavier ones are oily liquids. Alkanes even heavier than those on this list tend to be waxy solids, an example being paraffin wax, for making candles. It should be noted that from butane on up, the alkanes have numerous structural isomers, depending on\nwhether they are straight or branched, and these isomers have differing chemical properties.", "9e7a1e00-2a24-431f", "", "Branched alkanes are named by indicating the branch attached to the principal chain. Branches, known as substituents, are named by taking the name of an alkane and replacing the suffix with yl", "6a4e916b-4cfc-47d5", "", "for example, methyl, ethyl, and so on. The general term for an alkane which functions as a substituent is alkyl.", "AdThrive_Content_10_desktop", "adthrive-ad adthrive-content adthrive-content-10 adthrive-ad-cls", "e35f70a0-0f15-460a", "", "77f36370-d8d2-4447", "", "Cycloalkanes are alkanes joined in a closed loop to form a ring-shaped molecule. They are named by using the names above, with cyclo-as a prefix. These start with propane, or rather cyclopropane, which has the minimum number of carbon atoms to form a closed shape: three atoms, forming a triangle.", "51e989d3-2cfd-4429", "", "ALKENES AND ALKYNES.", "45bf4924-82a8-48be", "", "The names of the alkenes, hydrocarbons that contain one or more double bonds per molecule, are parallel to those of the alkanes, but the family ending is-ene. Likewise they have a common formula: C", "2c10a2e1-9582-4926", "", "1b45c6d6-5366-4c97", "", "2n", ". Both alkenes and alkynes, discussed below, are unsaturated", "56c55dd4-84c9-44f1", "", "in other words, some of the carbon atoms in them are free to form other bonds. Alkenes with more than one double bond are referred to as being polyunsaturated.", "a6bd8bae-2e9f-4296", "", "As with the alkenes, the names of alkynes (hydrocarbons containing one or more triple bonds per molecule) are parallel to those of the alkanes, only with the replacement of the suffix -yne in place of-ane. The formula for alkenes is C", "bde9b29e-3256-413f", "", "e11630d4-0d64-48d6", "", "2n-2", ". Among the members of this group are acetylene, or C", "1ebbee6c-ecef-418f", "", "74ab97b0-99e5-4da7", "", ", used for welding steel. Plastic polystyrene is another important product from this division of the hydrocarbon family.", "AdThrive_Content_11_desktop", "adthrive-ad adthrive-content adthrive-content-11 adthrive-ad-cls", "9f519fb1-61ad-4269", "", "b63f65ad-97be-4f15", "", "AROMATIC HYDROCARBONS.", "a1b2de91-683d-4e95", "", "Aromatic hydrocarbons, despite their name, do not necessarily have distinctive smells. In fact the name is a traditional one, and today these compounds are defined by the fact that they have benzene rings in the middle. Benzene has a formula C", "864e8219-86a9-4f26", "", "697b8335-27eb-4645", "", ", and a benzene ring is usually represented as a hexagon (the six carbon atoms and their attached hydrogen atoms) surrounding a circle, which represents all the bonding electrons as though they were everywhere in the molecule at once.", "f6e0773a-a73e-4c12", "", "In this group are products such as naphthalene, toluene, and dimethyl benzene. These last two are used as solvents, as well as in the synthesis of drugs, dyes, and plastics. One of the more famous (or infamous) products in this part of the vast hydrocarbon network is trinitrotoluene, or TNT. Naphthalene is derived from ", "/science-and-technology/chemistry/organic-chemistry/coal-tar", "a339c239-a098-4f27", "", "coal tar", ", and used in the synthesis of other compounds. A crystalline solid with a powerful odor, it is found in mothballs and various deodorant-disinfectants.", "6665115e-6b22-4385", "", "PETROCHEMICALS.", "3b5df0af-76e7-4089", "", "As for petro-chemicals, these are simply derivatives of petroleum, itself a mixture of alkanes with some alkenes, as well as aromatic hydrocarbons. Through a process known as fractional distillation, the petrochemicals of the lowest molecular mass boil off first, and those having higher mass separate at higher temperatures.", "AdThrive_Content_12_desktop", "adthrive-ad adthrive-content adthrive-content-12 adthrive-ad-cls", "2c509ceb-aa1b-49fb", "", "bd590c5b-179c-4a66", "", "Among the products derived from the fractional distillation of petroleum are the following, listed from the lowest temperature range (that is, the first material to be separated) to the highest: natural gas; petroleum ether, a solvent; naphtha, a solvent (used for example in paint thinner); gasoline; kerosene; fuel for heating and diesel fuel; lubricating oils; petroleum jelly; paraffin wax; and pitch, or tar. A host of other organic chemicals, including various drugs, plastics, paints, adhesives, fibers, detergents, synthetic rubber, and agricultural chemicals, owe their existence to petrochemicals.", "7d7838e2-f32a-4de2", "", "Obviously, petroleum is not just for making gasoline, though of course this is the first product people think of when they hear the word \"petroleum.\" Not all hydrocarbons in gasoline are desirable. Straight-chain or normal heptane, for instance, does not fire smoothly in an ", "/science-and-technology/technology/technology-terms-and-concepts/internal-combustion-engine", "552344b5-8250-42c0", "", "internal-combustion engine", ", and therefore disrupts the engine's rhythm. For this reason, it is given a rating of zero on a scale of desirability, while octane has a rating of 100. This is why gas stations list octane ratings at the pump: the higher the presence of octane, the better the gas is for one's automobile.", "0491001c-4bf4-4c15", "", "Hydrocarbon Derivatives", "c5d54cc2-9be3-4733", "", "With carbon and hydrogen as the backbone, the hydrocarbons are capable of forming a vast array of hydrocarbon derivatives by combining with other elements. These other elements are arranged in functional groups", "8903d3cc-8648-4b88", "", "an atom or group of atoms whose presence identifies a specific family of compounds. Below we will briefly discuss some of the principal hydrocarbon derivatives,\nwhich are basically hydrocarbons with the addition of other molecules or single atoms.", "AdThrive_Content_13_desktop", "adthrive-ad adthrive-content adthrive-content-13 adthrive-ad-cls", "ce1e8a38-cf2c-42f8", "", "98707851-fbcd-45cc", "", "Alcohols are oxygen-hydrogen molecules wedded to hydrocarbons. The two most important commercial types of alcohol are methanol, or wood alcohol; and ethanol, which is found in alcoholic beverages, such as beer, wine, and liquor. Though methanol is still known as \"wood alcohol,\" it is no longer obtained by heating wood, but rather by the industrial hydrogenation of carbon monoxide. Used in adhesives, fibers, and plastics, it can also be applied as a fuel. Ethanol, too, can be burned in an ", "1a5846b6-7f71-43a2", "", ", when combined with gasoline to make gasohol. Another significant alcohol is cholesterol, found in most living organisms. Though biochemically important, cholesterol can pose a risk to human health.", "0dd8ab5e-f50f-4e09", "", "Aldehydes and ketones both involve a double-bonded carbon-oxygen molecule, known as a ", "/science-and-technology/chemistry/organic-chemistry/carbonyl-group", "91e2cfe8-2524-499b", "", "carbonyl group", ". In a ketone, the ", "90306abb-043b-4091", "", " bonds to two hydrocarbons, while in an aldehyde, the carbonyl group is always at the end of a hydrocarbon chain. Therefore, instead of two hydrocarbons, there is always a hydrocarbon and at least one other hydrogen bonded to the carbon atom in the carbonyl. One prominent example of a ketone is acetone, used in nail polish remover. Aldehydes often appear in nature", "e03cf65c-b7b3-4a8c", "", "for instance, as vanillin, which gives vanilla beans their pleasing aroma. The ketones carvone and camphor impart the characteristic flavors of spearmint leaves and caraway seeds.", "AdThrive_Content_14_desktop", "adthrive-ad adthrive-content adthrive-content-14 adthrive-ad-cls", "e90dc0b6-87fc-4b0c", "", "bfa53d33-19db-4889", "", "CARBOXYLIC ACIDS AND ESTERS.", "654c5db4-6133-4981", "", "Carboxylic acids all have in common what is known as a ", "/science-and-technology/chemistry/organic-chemistry/carboxyl-group", "ffa3da1d-5606-4cc7", "", "carboxyl group", ", designated by the symbol -COOH. This consists of a carbon atom with a double bond to an oxygen atom, and a single bond to another oxygen atom that is, in turn, wedded to a hydrogen. All carboxylic acids can be generally symbolized by RCOOH, with R as the standard designation of any hydrocarbon. Lactic acid, generated by the human body, is a ", "/science-and-technology/chemistry/organic-chemistry/carboxylic-acid", "9b8be230-66bf-42bc", "", "carboxylic acid", ": when a person overexerts, the muscles generate ", "/science-and-technology/chemistry/organic-chemistry/lactic-acid", "d3b103d3-3f71-459c", "", "lactic acid", ", resulting in a feeling of fatigue until the body converts the acid to water and carbon dioxide. Another example of a ", "b000176b-051d-400b", "", " is ", "/science-and-technology/chemistry/organic-chemistry/butyric-acid", "246acf5c-0574-4d8c", "", "butyric acid", ", responsible in part for the smells of rancid butter and human sweat.", "43d9c31c-6ab9-41ea", "", "When a carboxylic acid reacts with an alcohol, it forms an ester. An ester has a structure similar to that described for a carboxylic acid, with a few key differences. In addition to its bonds (one double, one single) with the oxygen atoms, the carbon atom is also attached to a hydrocarbon, which comes from the carboxylic acid. Furthermore, the single-bonded oxygen atom is attached not to a hydrogen, but to a second hydrocarbon, this one from the alcohol. One well-known ester is acetylsalicylic acid", "d3c3f557-9bd7-4f26", "", "better known as aspirin. Esters, which are a key factor in the aroma of various types of fruit, are often noted for their pleasant smell.", "AdThrive_Content_15_desktop", "adthrive-ad adthrive-content adthrive-content-15 adthrive-ad-cls", "b1f38c0d-a757-4b7c", "", "84714b3f-c204-4351", "", "Polymers", "7d4d643c-7715-49a9", "", "Polymers are long, stringy molecules made of smaller molecules called monomers. They appear in nature, but thanks to Carothers", "7be33588-cc9b-4cb3", "", "a tragic figure, who committed suicide a year before Nylon made its public debut", "eba77d70-8d8f-44f0", "", "as well as other scientists and inventors, synthetic polymers are a fundamental part of daily life.", "44ffcef6-4c49-4d38", "", "The structure of even the simplest polymer, polyethylene, is far too complicated to discuss in ordinary language, but must be represented by chemical symbolism. Indeed, polymers are a subject unto themselves, but it is worth noting here just how many products used today involve polymers in some form or another.", "348301ee-beae-4174", "", "Polyethylene, for instance, is the plastic used in garbage bags, electrical insulation, bottles, and a host of other applications. A variation on polyethylene is Teflon, used not only in nonstick cookware, but also in a number of other devices, such as bearings for low-temperature use. Polymers of various kinds are found in siding for houses, tire tread, toys, carpets and fabrics, and a variety of other products far too lengthy to enumerate.", "AdThrive_Content_16_desktop", "adthrive-ad adthrive-content adthrive-content-16 adthrive-ad-cls", "03b958af-87dd-4ad7", "", "5c4e55df-d6bd-4224", "", "WHERE TO LEARN MORE", "5e64f1e9-8fd2-4cd9", "", "Blashfield, Jean F. ", "da616b11-cbe5-4296", "", "Carbon.", " Austin, TX: Raintree Steck-Vaughn, 1999.", "dcc261dc-97f4-4e6c", "", "406da75e-c03f-4506", "", "\"Carbon.\" Xrefer", " (Web site). <http://www.xrefer.com/entry/639742> (May 30, 2001).", "fd1dcbdf-4e35-4b88", "", "4a6f691a-aa1e-4b27", "", "Chemistry Help Online for Students", " (Web site). <http://members.tripod.com/chemistryhelp/> May 30, 2001).", "9a1acc24-6577-4ca4", "", "Knapp, Brian J. ", "12514c02-71d8-4d42", "", "Carbon Chemistry.", " Illustrated by David Woodroffe. Danbury, CT: Grolier Educational, 1998.", "6c96abbf-20f8-48c8", "", "Loudon, G. Marc. ", "6a38e00a-6ff9-4996", "", "Organic Chemistry.", " Menlo Park, CA: Benjamin/Cummings, 1988.", "63a335ab-b0a6-472d", "", "517670de-03b8-4457", "", "\"Organic Chemistry\"", " (Web site). <http://edie.cprost.sfu.ca/~rhlogan/organic.html> (May 30, 2001).", "646dacaf-eadb-46b0", "", "6d319ccb-adb1-4433", "", "\"Organic Chemistry.\" Frostburg State University Chemistry Helper", " (Web site). ", "http://www.chemhelper.com/", "73c2046e-af2b-45c8", "", "<http://www.chemhelper.com/>", " (May 30, 2001).", "AdThrive_Content_17_desktop", "adthrive-ad adthrive-content adthrive-content-17 adthrive-ad-cls", "4a163e3e-4f7e-4e3d", "", "220eff8c-7dbf-46b9", "", "Sparrow, Giles. ", "3f0d692a-dddc-4eda", "", "1215767", "/places/united-states-and-canada/us-political-geography/new-york", "c62c18f9-5482-4e25", "", "New York", ": Benchmark Books, 1999.", "c8c8e447-922a-4760", "", "Zumdahl, Steven S. ", "136d8ddf-3e9d-4fe4", "", "Introductory Chemistry: A Foundation,", " 4th ed. Boston: Houghton Mifflin, 2000.", "9167d51f-67ff-4986", "", "KEY TERMS", "afb73aad-f56e-43a1", "", "ALKANES:", "15169f72-cdbe-46ee", "", "Hydrocarbons that form single bonds. Alkanes are also called saturated hydrocarbons.", "9080269c-665a-440d", "", "ALKENES:", "b6e22b6e-6d20-4b4f", "", "Hydrocarbons that form double bonds.", "13769872-ba17-4c58", "", "ALKYL:", "10f21d05-8cef-440d", "", "A general term for an alkane that functions as a substituent.", "6570fb2f-94ec-488e", "", "ALKYNES:", "a3bd9e0b-addc-495e", "", "Hydrocarbons that form triple bonds.", "AdThrive_Content_18_desktop", "adthrive-ad adthrive-content adthrive-content-18 adthrive-ad-cls", "83fb1802-0808-4116", "", "e8c06ac0-4df0-4084", "", "ALLOTROPES:", "964cf8b0-f671-43bb", "", "Different versions of the same element, distinguished by molecular structure.", "e4d66b1d-af70-4ad9", "", "AMORPHOUS:", "65c9201a-2014-4b45", "", "Having no definite structure.", "0dc3064c-2d9e-43bf", "", "COVALENT BONDING:", "20645f3f-d972-4e33", "", "A type of chemical bonding in which two atoms share valence electrons.", "6abe6027-f860-4332", "", "CRYSTALLINE:", "d51a082c-a757-4237", "", "A term describing a type of solid in which the constituent parts have a simple and definite geometric arrangement repeated in all directions.", "c2906b25-fcee-4289", "", "DOUBLE BOND:", "92a65b89-d245-4e2b", "", "A form of bonding in which two atoms share two pairs of valence electrons. Carbon is also capable of single bonds and triple bonds.", "17921d80-eb4d-44d7", "", "ELECTRONEGATIVITY:", "872d5c7b-5885-48aa", "", "The relative ability of an atom to attract valence electrons.", "AdThrive_Content_19_desktop", "adthrive-ad adthrive-content adthrive-content-19 adthrive-ad-cls", "5ef1ac31-b944-496f", "", "2ca0f84e-295d-4c94", "", "FUNCTIONAL GROUPS:", "9bcb122f-2ed3-4d88", "", "An atom or group of atoms whose presence identifies a specific family of compounds.", "004a7f55-b131-40e9", "", "HYDROCARBON:", "00d8a2b4-807a-4961", "", "Any chemical compound whose molecules are made up of nothing but carbon and hydrogen atoms.", "ed40e3cb-4608-415a", "", "HYDROCARBON DERIVATIVES:", "5213d762-8a1d-41f8", "", "Families of compounds formed by the joining of hydrocarbons with various functionalgroups.", "27644370-3af1-4580", "", "ISOMERS:", "a1eaabd7-7d32-4a2c", "", "Substances having the same chemical formula, but that are different chemically due to disparities in the arrangement of atoms.", "ff63a391-d525-4c0c", "", "OCTET RULE:", "c912b4a7-a6a9-42b5", "", "A term describing the distribution of valence electrons that takes place in chemical bonding for most elements, which end up with eight valence electrons.", "AdThrive_Content_20_desktop", "adthrive-ad adthrive-content adthrive-content-20 adthrive-ad-cls", "cdbfecb9-910c-4c7a", "", "bd89c53b-047e-4387", "", "ORGANIC CHEMISTRY:", "dfe6fcfe-d1f2-4665", "", "The study of carbon, its compounds, and their properties. (Some carbon-containing compounds, most notably oxides and carbonates, are not considered organic.)", "482f2754-c71b-4edf", "", "SATURATED:", "ae7a7e17-138f-4a3d", "", "A term describing a hydrocarbon in which each carbon is already bound to four other atoms. Alkanes are saturated hydrocarbons.", "d3b46e58-f4b9-4943", "", "SINGLE BOND:", "932e412a-b9d9-485f", "", "A form of bonding in which two atoms share one pair of valence electrons. Carbon is also capable of double bonds and triple bonds.", "8d115b1c-52a2-4596", "", "SUBSTITUENTS:", "2b5c4abd-be2a-4f17", "", "Branches of alkanes, named by taking the name of an alkane and replacing the suffix with yl", "e6e725a8-61f2-4e49", "", "for example, methyl, ethyl, and so on.", "3bd41f64-83e2-490a", "", "TETRAVALENT:", "31e35314-3f4b-4fce", "", "Capable of bonding to four other elements.", "AdThrive_Content_21_desktop", "adthrive-ad adthrive-content adthrive-content-21 adthrive-ad-cls", "3b4b6e10-f611-47fc", "", "25c2c948-d7ea-44d1", "", "TRIPLE BOND:", "942161c0-014e-4268", "", "A form of bonding in which two atoms share three pairs of valence electrons. Carbon is also capable of single bonds and double bonds.", "e560a28a-b1d7-457e", "", "UNSATURATED:", "666a150c-3ba7-4adf", "", "A term describing a hydrocarbon in which the carbons involved in a multiple bond (a double bond or triple bond) are free to bond with other atoms. Alkenes and alkynes are bothunsaturated.", "537a8346-4d25-4a82", "", "VALENCE ELECTRONS:", "30a9d9fa-f57e-4090", "", "Electrons that occupy the highest principal energy level in an atom. 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", "160cce68-961b-410a", "", "Encyclopedia.com.", " 29 Jun. 2023 ", "0b2e393d-957c-4a04", "", "<", "https://www.encyclopedia.com", "2a91a313-a908-4716", "", "f4d60bdf-6dec-4740", "", ">", ".", "tab-pane", "chicagoTab0", "45c91cc7-b707-4440", "", "1aa7aa8d-639c-4fb6", "", " \"Organic Chemistry\n.\" ", "e027c7b5-56c4-42c2", "", "048eeeed-1e3e-4865", "", " (June 29, 2023). ", "4db3ef42-a8c7-4616", "", "https://www.encyclopedia.com/science/news-wires-white-papers-and-books/organic-chemistry-0", "apaTab0", "375f154f-82b6-4607", "", "000fb597-e5eb-4079", "", "6f740e27-c4a4-451f", "", ". . 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Then, copy and paste the text into your bibliography or works cited list.", "231e21db-f29d-461d", "", " Because each style has its own formatting nuances that evolve over time and not all information is available for every reference entry or article, Encyclopedia.com cannot guarantee each citation it generates. Therefore, it\u2019s best to use Encyclopedia.com citations as a starting point before checking the style against your school or publication\u2019s requirements and the most-recent information available at these sites:", "47df6976-66b5-4d03", "", "091ceba6-3225-4a34", "", "Modern Language Association", "7bc46d3f-80ce-4abc", "", "target", "_blank", "http://www.mla.org/style", "aa65fe65-df0a-4bce", "", "ad5d5a3c-c596-4b70", "", "The Chicago Manual of Style", "73493d69-27e8-49e6", "", "http://www.chicagomanualofstyle.org/tools_citationguide.html", "cb521f97-3544-4b3a", "", "391ec45b-b7aa-4c6d", "", "American Psychological Association", "32303317-a76a-4c31", "", "http://apastyle.apa.org/", "95c64c53-ab30-4d0c", "", "H5", "d88d89bd-e50e-4a12", "", "Notes:", "citationnotes", "4ee5f486-3fea-4683", "", "aa1fbf6e-02fa-45ee", "", " Most online reference entries and articles do not have page numbers. Therefore, that information is unavailable for most Encyclopedia.com content. However, the date of retrieval is often important. Refer to each style\u2019s convention regarding the best way to format page numbers and retrieval dates.", "c9ef05ec-83b5-4dad", "", " In addition to the MLA, Chicago, and APA styles, your school, university, publication, or institution may have its own requirements for citations. Therefore, be sure to refer to those guidelines when editing your bibliography or works cited list.", "modal-footer", "e5d45d12-1752-4e7c", "", "label-citation", "a24c71f2-aeb1-4a6d", "", "icon-citation", "d7d37389-772e-4137", "", "copy-citation", "1a1277fe-178a-4290", "", "fas fa-copy", "cf5f3f11-0f3e-4f42", "", "articleWrapper-393585", "7cb707da-ae68-4f18", "", "1G23400900367", "975b534d-ab0d-4e53", "", "doctitle collapsed", "#collapseExample1", "multiCollapseExample1", "2dd33528-ded7-48f3", "", "fd2fc698-4afc-4932", "", "92e23679-025f-4d4f", "", "c8d68c91-3c4b-4869", "", "466cb821-3e12-4c4a", "", "a2d77004-e94f-40cb", "", "4af026e4-2817-4255", "", "3,397,478", "b5c8ae0e-f2dd-4e9a", "", "b2c6be72-cc52-42ab", "", "May 29 2018", "0324c2aa-0704-423e", "", "e0cf4f6a-44c5-4fbd", "", "9acb5782-2692-45f2", "", "a5844a39-5380-4174", "", "adfc0e65-e507-4401", "", "08491e3e-24cc-40c3", "", "#citationModal1", "50ece0a0-f8e3-49f3", "", "310a5519-96e2-4008", "", "b0bad5a9-9e62-4497", "", "80006024-347f-4b89", "", "12d6e9f5-2221-47c2", "", "666e9071-6ac8-4555", "", "2f3b53fb-be6a-4834", "", "collapseExample1", "6c0937ad-bc50-4a7c", "", "ef0d3fc6-9427-448c", "", "HR", "0a387ea3-0c95-4978", "", "c702dca2-d14e-44ef", "", "Organic chemistry is the chemistry of carbon compounds. 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mixtures of ", "/science-and-technology/chemistry/organic-chemistry/methyl-alcohol", "b532c8ac-6b4d-4ccf", "", "methyl alcohol", ", acetone, and ", "/science-and-technology/chemistry/organic-chemistry/acetic-acid", "84ed687f-b966-43a4", "", "acetic acid", ". Alchemists isolated cholesterol from gallstones, morphine from opium, and drugs such as quinine, strychnine, and brucine from various plants. Two hundred years ago chemists such as Antoine Lavoisier determined the elemental composition of many of these substances and noted that they all contained carbon and hydrogen, and that many also contained oxygen and nitrogen. It also appeared that there were two classes of materials: the mineral type (generally hard, high-melting, and noncombustible), and the organic type (often soft, liquid or low melting solids, and frequently easily combustible materials). Most organic chemicals could be burned to produce ", "4182e79c-3ae4-4585", "", "; and any hydrogen present was converted to water (H", "6a9dda13-9fde-4f93", "", "O). Because organic compounds had for centuries been isolated only from plants and animals, it was commonly believed that some \"vital force\" in living things was necessary to produce them. This belief persisted until 1828, when Friedrich W", "e3021618-e80b-4340", "", "hler was able to make urea, a chemical found in the urine of animals, from the inorganic salt ammonium cyanate.", "AdThrive_Content_23_desktop", "adthrive-ad adthrive-content adthrive-content-23 adthrive-ad-cls", "23153616-cafa-4dcc", "", "3d918e47-c89b-4f30", "", "Since that time ", "a42c8dd3-9aed-4874", "", " has grown into a vast and ever expanding field that encompasses millions of chemical compounds.", "59cc55e0-f293-4a90", "", "Scope of Organic Chemistry", "339695a2-13db-4853", "", "The field of ", "5447c0f9-b087-48a5", "", " includes more than twenty million compounds for which properties have been determined and recorded in the literature. Many hundreds of new compounds are added every day. Much more than half of the world's chemists are organic chemists. Some new organic compounds are simply isolated from plants or animals; some are made by modifying naturally occurring chemicals; but most new organic compounds are actually synthesized in the laboratory from other (usually smaller) organic molecules. Over the years organic chemists have developed a broad array of reactions that allow them to make all kinds of complex products from simpler starting materials.", "00761a8d-a7bf-4eb2", "", "Singular Attributes of Carbon", "8c5e44e6-f762-4898", "", "When one considers the millions of chemical compounds that are known and notes that more than 95 percent of them are compounds of carbon, one realizes that carbon is unique. Why are there so many carbon compounds? It turns out that atoms of carbon are quite remarkable in a number of ways.", "AdThrive_Content_24_desktop", "adthrive-ad adthrive-content adthrive-content-24 adthrive-ad-cls", "0457db81-cc5d-4b6b", "", "BLOCKQUOTE", "b22151ce-9822-412d", "", "e7130c22-2b7e-4459", "", "Carbon atoms form very strong bonds with other carbon atoms. The bonds are so strong that carbon can form long chains, some containing thousands of carbon atoms. (Carbon is the only element that can do this.)", "3305fac3-1eab-4119", "", "A carbon atom forms four bonds, therefore carbon not only can form long chains, but it also forms chains that have branches. It is a major reason why carbon compounds exhibit so much isomerism. The simple compound decane (C", "3b474a44-7313-4f25", "", "640c06f1-57c1-4c99", "", "22", "), for example, has 75 different ", "e8c4625a-0242-4f83", "", "isomers", " .", "2c86855b-f095-4528", "", "Carbon atoms can be bonded by double or triple bonds as well as single bonds. This multiple bonding is much more prevalent with carbon than with any other element.", "5533f7b3-94ff-4a74", "", "Carbon atoms can form rings of various sizes. The rings may be saturated or unsaturated. The unsaturated 6-membered ring known as the benzene ring is the basis for an entire subfield of \"aromatic\" organic chemistry.", "c7be16a6-6274-4370", "", "Carbon atoms form strong bonds not only with other carbon atoms but also with atoms of other elements. In addition to hydrogen, many carbon compounds also contain oxygen. Nitrogen, sulfur, phosphorus, and the halogens also frequently occur in carbon compounds.", "AdThrive_Content_25_desktop", "adthrive-ad adthrive-content adthrive-content-25 adthrive-ad-cls", "49eeb64e-cbd6-44b6", "", "fa5ea162-03c3-41b9", "", "Various kinds of ", "9fffd845-e680-4d1d", "", "functional groups", " occur widely among carbon compounds, and many different kinds of isomers are possible.", "c09a4ffd-b7a5-4dc0", "", "eb37f728-bc8e-4a88", "", "Compounds of carbon and hydrogen only are called ", "a84f0b47-a66e-4396", "", "hydrocarbons.", " These are the simplest compounds of organic chemistry. The most basic group of hydrocarbons are the ", "158e94ac-a561-4b4b", "", "alkanes,", " which contain only single bonds. The simplest member of the alkane series is methane, CH", "538a8f29-ac84-452e", "", ", the main component of ", "2fe43a00-9a24-47d1", "", ". The names of some alkanes are listed in Table 1. Alkanes sometimes", "TABLE", "5b178a43-c80b-459b", "", "THEAD", "cc385479-8f9b-4cf3", "", "TR", "21f90ee2-cff0-413f", "", "TD", "rowspan", "colspan", "addd39cf-8c77-4025", "", "60ba20c4-a797-4bd3", "", "ALKANES", "6cf56db4-d7b0-41ff", "", "51fff9a5-76dc-4d8a", "", "f4dc01b4-9b08-44ed", "", "Formula", "91682727-7910-4989", "", "21a7aa25-5611-4781", "", "Name", "TBODY", "30321654-b249-434e", "", "15015942-c03e-414c", "", "f713d724-e853-42c3", "", "CH", "4161bfba-0dcf-4564", "", "10e8ecd1-126e-498c", "", "4cdd9ab1-d397-4e06", "", "7b19dcf6-f15b-4361", "", "methane", "010221f9-8263-4478", "", "gases", "27f93bca-c16e-4f1a", "", "b5beda73-691b-49a6", "", "C", "20577e7a-4c99-4dde", "", "71711447-529c-4431", "", "8285ca8b-8405-48c6", "", "5c3042cd-0775-4a0c", "", "ac43dbbd-b7a9-4adb", "", "64b8d108-6128-47c4", "", "ethane", "7d1a0777-680f-4d92", "", "d5e7da89-3000-4205", "", "91a2269b-7c71-414d", "", "faa3ff18-b6bf-4cf7", "", "8077cca1-16f6-44a3", "", "6b95127f-2218-4cf7", "", "1f3065a9-4c92-4fa0", "", "59b5494a-19fc-4c68", "", "4bf1d855-e65f-40ec", "", "propane", "f4a8744b-7925-445e", "", "5bd01f30-d058-464c", "", "d3a61b7c-467e-4446", "", "816abe89-585b-4224", "", "e2c6cece-eb75-4af9", "", "7255f308-fb1e-46e8", "", "7dfb073f-ed08-484e", "", "33798451-6909-41c0", "", "ce9b8fa3-7a8c-46ed", "", "5fe2671d-fa96-488e", "", "butane", "d653a977-b75d-4c99", "", "07a4b7d3-7adc-41cc", "", "8b2f365e-7f2c-440a", "", "e2e77fff-417c-4486", "", "0b1c9ff6-b0f8-41aa", "", "1709eefb-62c4-4f6e", "", "(CH", "f1808f93-b012-4526", "", "684f3580-0eda-4b00", "", "89b01991-e504-4a83", "", "e0a297bc-2ab1-4aef", "", "pentane", "13", "f9c60d99-a7ca-4a92", "", "liquids", "0d1b10d2-8ae4-4353", "", "c8245504-fd9d-49f2", "", "12c22b0d-efe8-4d44", "", "50544abb-f689-4353", "", "46eca98d-aa22-423d", "", "46700fdd-7615-4af5", "", "a173c55f-e021-4578", "", "a4131488-782b-4366", "", "95480aa1-b8e4-413f", "", "129a220b-ba6b-4a3b", "", "hexane", "9a9f8252-3a0b-48f2", "", "85f8dc0b-50c2-4649", "", "0746fc13-1b92-4ea7", "", "2f61a368-7c27-45fd", "", "9b73ea5e-680c-45b4", "", "971dcaf2-2897-48b5", "", "bd9a3378-8013-43d6", "", "1247f5aa-7ef8-4327", "", "d4483846-780a-4530", "", "9ccbf8f4-3906-457d", "", "heptane", "89269dbe-81c2-4bdb", "", "70cbc89f-ffd7-4b08", "", "55c080cd-d2c9-4dde", "", "9922b8a4-c153-4ab4", "", "03ded97c-bba6-425f", "", "c1146b1d-bfc1-4260", "", "b655c391-2f20-4119", "", "16167eb4-e028-42e6", "", "acba3e32-fdca-40c8", "", "0122ac93-209c-46df", "", "octane", "629e45be-1836-468a", "", "c79358e4-1de4-40ed", "", "34a96a8c-ca0e-4a74", "", "9", "cd79bd9b-9bdc-4dde", "", "45f05a0e-51be-4cb2", "", "094c93f3-2343-4ae7", "", "fdac45ef-65e5-4d79", "", "7aeb1185-2bb1-4b88", "", "09fbf451-9076-47b1", "", "31be7265-927b-4f9e", "", "nonane", "13fcee5b-ded8-48a2", "", "b05761b5-a913-414e", "", "375c1660-3aa2-4027", "", "4f48aa45-2ed4-4c18", "", "56605530-ce92-4e14", "", "4e442bc3-1c6a-48c7", "", "91f8e0cc-182e-44a8", "", "33b94675-60ae-467c", "", "3eaa3a90-48c8-4f37", "", "254631ea-493b-4877", "", "decane", "a428ce19-f3e8-4a6a", "", "0bbf8cf2-78d6-4117", "", "3df78b38-a50b-46f6", "", "11", "b10f0ec2-234d-42c1", "", "60c499ac-c90f-458a", "", "b926e5c5-9edc-4a0e", "", "060583d1-8a74-4ceb", "", "6c1e1668-cb3d-4b16", "", "40574237-89d1-401c", "", "b7b64237-4b89-495a", "", "undecane", "efa6f13e-a7fc-475d", "", "f3c8df58-243c-4d62", "", "00e9fb11-73cc-4993", "", "8223d92c-abaf-4ae1", "", "26", "5f0c60d4-deef-451d", "", "242ad1b1-f3a2-4ac3", "", "f81131ef-053f-45fa", "", "f336a0d6-674c-4b5f", "", "63caaca5-594e-4d4e", "", "a872b590-8e10-474a", "", "dodecane", "0fe583b7-6023-4261", "", "6d46be61-62bd-4b2c", "", "6a52fe82-06be-4731", "", "a1f9d532-2d75-4edf", "", "28", "983d9f05-a402-40df", "", "3d12cf81-07bc-4bfe", "", "e8f5178b-2023-4446", "", "d9451c2c-3695-4a13", "", "a5552586-35ae-41e4", "", "83ff1186-b364-4654", "", "tridecane", "3c17af7b-c824-4f2e", "", "4b5bb948-d887-45c8", "", "0654aa69-4440-4a5d", "", "f3bdc257-5f20-4608", "", "30", "531de9f9-912f-4d40", "", "49424423-21fa-4172", "", "7e13481e-b5db-4e15", "", "5c4b241e-5d8d-467f", "", "c8c52efa-a2da-4d06", "", "f2be314d-734a-4024", "", "tetradecane", "3e5edbed-593a-4026", "", "f43cb72a-bf2d-41a9", "", "5d3e77e7-f496-4907", "", "bc4fe814-912b-4bba", "", "32", "53ca9c72-9c60-4b4c", "", "48058b6d-78a3-412d", "", "40cd1db3-9e39-4e9b", "", "c4ae4c93-4119-43d5", "", "a7f1a818-3783-4d1b", "", "129fcd03-11ba-4f69", "", "pentadecane", "8ed27aca-39b4-4f0f", "", "4f6d4091-54e3-467a", "", "787476b0-82f3-4d77", "", "12cd23ed-bc13-4d20", "", "34", "b5370363-12aa-4f4f", "", "a0b2a2d1-e78a-4d9e", "", "f63c3636-442a-4eb3", "", "ee5164a3-b294-4ae6", "", "194b68b2-53b9-40f9", "", "08078b39-b260-42f8", "", "hexadecane", "f8c147e5-f0c7-4607", "", "404e4382-893a-49a8", "", "74af884b-379f-4562", "", "17", "b42d57d7-b7c8-49cf", "", "36", "df4ea91a-4925-40aa", "", "7d336e07-2ec1-41a2", "", "3d18f38d-2fa3-4ed5", "", "4517e15b-2925-478b", "", "e3cea83b-493b-4612", "", "84852f14-d646-4991", "", "heptadecane", "26cf052e-80d7-4596", "", "fe62a6c3-a4be-4d41", "", "7f5eabfb-55de-407c", "", "af6cbd81-e722-433d", "", "38", "6315f08c-cdfa-45c4", "", "0ad3c687-7226-47c4", "", "1214647e-d5ee-4fc0", "", "713cba7b-0072-471f", "", "02da854a-7f1b-4898", "", "a53a99c9-fdcd-482f", "", "octadecane", "e1f59d06-83fa-494a", "", "solids", "1fb3044f-55f8-4fcd", "", "d7d50776-faee-47e0", "", "5babdcdd-5452-46b2", "", "19", "84b4f649-b149-4245", "", "40", "56bee69d-d2cc-42ce", "", "ff480814-3604-4dbb", "", "37b169b4-c7a9-4734", "", "99421e8c-c78f-4df8", "", "1a13eaf6-c6dc-474d", "", "c9258c33-424f-4384", "", "nonadecane", "f4d1262c-afcf-410b", "", "34e76795-47ce-49b7", "", "a332cbf9-e7b5-486f", "", "49635837-26cd-40b8", "", "42", "7d2394bc-1921-4f3a", "", "621aeb41-7f0a-418a", "", "409ac0e3-373a-4d28", "", "02bf80ba-f7f5-4fb7", "", "6f48189f-d759-42a6", "", "34e501e8-38fc-413f", "", "eicosane", "52ed2022-2b2c-4487", "", "have ring structures. Since a 4-carbon chain of the alkane series is called ", "91976dc1-a0e6-4bc4", "", "butane,", " a ring of 4 carbon atoms is called ", "c0edd246-ff48-4cae", "", "cyclobutane.", "AdThrive_Content_26_desktop", "adthrive-ad adthrive-content adthrive-content-26 adthrive-ad-cls", "b51865a5-e44c-4918", "", "dfa988dc-aa6f-4166", "", "Simple hydrocarbons that contain one or more double bonds are called ", "773d46e8-9004-4746", "", "alkenes.", " They are named like alkanes, but their names end in \" ", "66aeae4d-9508-4cd2", "", "\u2013", "ene.\" The simplest alkene has two carbon atoms and is called ", "89e56449-60a4-4849", "", "ethene.", " A 3-carbon chain that has a double bond is called ", "c0437bec-a90d-4bb0", "", "propene.", "1cb389d0-d421-420e", "", "A 5-carbon hydrocarbon chain with a double bond is called ", "bac9a30c-79c1-4523", "", "pentene,", " and if the double bond links the second and third carbons, it is 2-", "964e9f26-17b2-456a", "", "pentene.", " Like cycloalkanes, alkenes have the general formula C", "200d2c4a-06dd-4a8d", "", "19cff23f-3f1c-4996", "", ". Alkenes having ring structures are called ", "10a0a81d-cb01-4514", "", "cycloalkenes.", " A 5-carbon ring with a double bond is called ", "f924f4ef-3ae5-4965", "", "cyclopentene.", "ccf21302-941b-4938", "", "Hydrocarbons that contain one or more triple bonds are called ", "ef3f2d85-e217-4251", "", "alkynes,", " and is the name ending is \"", "d576e174-fbc2-463b", "", "yne.\" A 2-carbon alkyne is therefore named ", "1ebc7278-7bec-4cef", "", "ethyne.", " (However, the compound is often referred to by its common name, which is ", "744c443e-5c8d-4e34", "", "acetylene.", " )", "975d2df1-6e9a-469e", "", "Compounds that contain double or triple bonds are said to be \"unsaturated\"", "efad87c1-cad8-4509", "", "because they are not \"saturated\" with hydrogen atoms. Unsaturated compounds are reactive materials that readily add hydrogen when heated over a ", "ac30513c-d784-4f92", "", "catalyst", " such as nickel. The reverse reaction also occurs. Heating ethane with steam is an important commercial process for making ethene (or ethylene). This is an important commercial process called \"steam cracking.\"", "AdThrive_Content_27_desktop", "adthrive-ad adthrive-content adthrive-content-27 adthrive-ad-cls", "79d562a8-9bc4-4eb0", "", "1cd1dd67-6a73-435e", "", "When a 6-carbon ring contains 2 double bonds, it is called ", "8ccd891a-948e-4895", "", "cyclohexadiene,", " but when it has 3 double bonds, it is not called cyclohexatriene; this is because a 6-carbon ring with three double bonds takes on a special kind of stability. The double bonds become completely conjugated and no longer behave as double bonds. The ring, known as a \"benzene ring,\" is said to be aromatic.", "c4821b2a-97d8-4382", "", "The removal of a hydrogen atom from a hydrocarbon molecule leaves an ", "/science-and-technology/chemistry/organic-chemistry/alkyl-group", "4e3e18ba-e2d7-4a6b", "", "alkyl group", " that readily attaches to a functional group, or forms a branch on a hydrocarbon chain. The groups are named after the corresponding hydrocarbons. For example, CH", "f3f7c3a0-468c-43a9", "", "bda9c8c2-c4e3-4127", "", " is named ", "ed246ef0-e24c-441a", "", "methyl;", " CH", "838edc95-db27-4d70", "", "a71ec27f-4de8-45bb", "", "cdefec1c-d363-454d", "", ", ", "0ef54e80-1eca-4896", "", "ethyl;", "9d68908d-84c0-4e19", "", "= CH", "c2afd8a4-1e29-43e4", "", "3158794b-7242-4f0b", "", "ethenyl;", "b86ecab2-6076-4ad5", "", "c3c7b294-6bf5-480d", "", "9391598e-f52d-4103", "", "70a73b75-1b31-4d36", "", "859c5f76-250c-4b15", "", "propyl;", " and so on. A benzene ring from which a hydrogen atom has been removed is often referred to as a ", "31d631f0-76ac-4f09", "", "phenyl.", " The branched molecules shown here would be given names as follows", "4670c596-17b7-4c88", "", "Theoretically there is no limit to the length of hydrocarbon chains. Very large hydrocarbon molecules (polymers) have been made containing as many as 100,000 carbon atoms. However, such molecules are hard to make and very difficult to melt and to shape into useful products.", "2ceadfca-de35-4665", "", "Hydrocarbons are obtained primarily from fossil fuels", "ed2c784a-6462-4402", "", "especially petroleum and ", "741430ed-32f7-4efd", "", ". Natural gas is a mixture that is largely methane mixed with varying amounts of ethane and other light hydrocarbons, while petroleum is a complex mixture of many different hydrocarbons. ", "1210342", "/earth-and-environment/minerals-mining-and-metallurgy/mineralogy-and-crystallography/coal", "a8089a56-ef5c-4dc6", "", "Coal", ", the other fossil fuel, is a much more complicated material from which many kinds of organic compounds, some of them hydrocarbons, can be obtained.", "7ec1d923-5d9c-4d77", "", "Functional Groups", "26116780-2506-4f63", "", "Alkane molecules are rather unreactive (except for being very flammable), but alkenes react with many other substances. When a drop of bromine is added to an alkene, for example, the deep orange color of the bromine immediately disappears as the bromine adds across the double bond to form a dibromo derivative. The double bond is called a \"functional group\" because its presence in a molecule causes reactivity at that particular site. There are a dozen or so functional groups that appear frequently in organic compounds. Some of the most common ones are listed in Table 2. The same molecule may contain several functional groups. Aspirin, for example, is both a ", "0562de8f-6162-406a", "", "39ea0bf0-984e-4f63", "", " and an ", "1cafb4d8-1e35-474d", "", "ester", " , and cholesterol is an alkene as well as an alcohol.", "b5a2ab69-6c67-43a8", "", "Isomerism", "a1dda99a-50b8-476a", "", "Isomers are molecules with the same molecular formula but different structures. There is only one structure for methane, ethane, or propane; but butane, C", "8dc33b4d-09e2-4f11", "", "81ee9bbf-d839-4f81", "", ", can have either of two different structure:", "e741d0ed-a9fb-42b3", "", "The linear molecule (1) is called butane, or ", "29102926-149b-4ec5", "", "normal", " butane (", "ca2a366a-9fed-4bcd", "", " -butane), whereas the branched molecule (2) is methylpropane (rather than 2-methylpropane, as the methyl group has to be in a 2-position). If the methyl group of (2) were attached to a terminal carbon, the resultant molecule would be the same as (1). Methylpropane (2) is also called ", "31a2259f-160e-4a8d", "", "iso", " butane.", "72f3a7f8-a45b-4dbe", "", "In a conjugated system, there are alternating double and single bonds, allowing electrons to flow back and forth. Molecules that contain such conjugated systems are said to be stabilized by \"resonance.\" In the benzene ring every other bond is a double bond, all the way around the ring. This results in a special kind of stabilization called \"aromaticity,\" in which the electrons are delocalized and free to travel all around the ring. Certain ring compounds, like benzene, that contain such a conjugated system of double and single bonds are described as \"aromatic.\"", "f42d3eee-8f7e-4632", "", "Pentane has 3 isomers: pentane (or ", "872c18cb-f5d1-483d", "", " -pentane), methylbutane (or ", "c7efddaf-b361-4fb8", "", "iso-", " pentane), and dimethyl propane (or ", "19c640ed-ffaa-49c9", "", "neo", " pentane). Hexane has 5 isomers: hexane, 2-methylpentane, 3-methylpentane, 2,2-dimethylbutane, and 2,3-dimethylbutane. Heptane has 9 different isomers, octane has 18, nonane has 35, and decane has 75. An increase in the number of carbon atoms greatly increases the possibilities for isomerism. There are more than 4,000 isomers of C", "f536bac8-22d7-4330", "", "82f8da7b-3efb-4199", "", " and more than 366,000 isomers of C", "c207261a-66d6-450e", "", "34746576-0d29-43a3", "", ". The formula C", "ad81c963-f554-4cc5", "", "2c6f665a-c126-4b2c", "", "62", " has more than 4 billion. Of course, most of them have never been isolated as pure compounds (but could be, if there were any point in doing it).", "9b251039-9509-429c", "", "For molecules other than hydrocarbons, still other kinds of isomers are possible. The simple formula C", "c59fc6ec-5100-44d0", "", "f34f7c24-be95-44c3", "", "O can represent ethyl alcohol or dimethyl ether; and C", "09d1217b-2228-47cf", "", "4a4b0966-c88a-4ce8", "", "O could stand for an alcohol, an ether, an ", "3b45e0df-efbe-4e5a", "", "aldehyde", " , or a ", "58cc95d6-2290-4faf", "", "ketone", " (among other things). The larger a molecule is, and the greater the variety of atoms and functional groups it contains, the more numerous its isomers.", "8f82b278-6fbf-4bf9", "", "There is still another kind of isomerism that stems from the existence of \"right-\" and \"left-handed\" molecules. It is sometimes referred to as ", "5269e47f-7dd8-4a7d", "", "optical", " isomerism because the molecules that make up a pair of these isomers usually differ only in the way they rotate plane polarized light.", "96bffa8f-13cd-457f", "", "Nomenclature", "9f05d20d-0798-4d59", "", "There are so many millions of organic compounds that simply finding names for them all is a major challenge. It was not until the late nineteenth century that chemists developed a logical system for naming organic compounds. Compounds had often been named according to their sources. The 1-carbon ", "12162724-f505-43e6", "", ", for example, was first obtained from ants, and so it was called ", "f3831a4c-c858-4d9d", "", "formic", " acid, from the Latin word for ants (", "1ea22964-d6df-42af", "", "formicae", " ). The 2-carbon acid was obtained from vinegar (", "29284c1e-8200-4f5d", "", "acetum", " in Latin), and was called ", "e62def48-66f7-4d09", "", "acetic", " acid.", "7cdc0579-0013-439f", "", "To bring some order to the naming process an international meeting was held in 1892 at Geneva, ", "1208046", "/places/germany-scandinavia-and-central-europe/swiss-political-geography/switzerland", "12759849-5b33-42ba", "", "Switzerland", ". The group later became known as the International Union of Pure and Applied Chemistry (IUPAC). Its objective was to establish a naming process that would provide each compound with a unique and systematic name. An initial set of rules was adopted at that first meeting in Geneva, and IUPAC has continued that work. Its systematic naming rules are used by organic chemists all over the world. The names of the alkanes form the basis for the system, with functional groups usually being indicated with appropriate suffixes. Some examples are given in Table 2.", "e53a73ab-7a53-4f42", "", "Organic Reactions", "af94e902-081d-46f2", "", "Organic chemistry is concerned with the many compounds of carbon, their names, their isomers, and their properties, but it is mostly concerned with their reactions. Organic chemists have developed a huge array of chemical reactions that can convert one organic compound to another. Some reactions involve addition of one molecule to another; some involve decomposition of molecules; some involve substitution of one atom or group by another; and some even involve the rearrangement of molecules, with some atoms moving into new positions. Some reactions require energy in the form of heat or radiation; and some require a special kind of catalyst or some sort", "d83f6e1c-6224-4685", "", "ec977dad-7d7e-43a2", "", "885e54a6-3dda-429c", "", "2cf05f8b-c01e-43eb", "", "2e921021-1d1d-4d95", "", "NAMING ORGANIC COMPOUNDS", "90b85551-f443-4536", "", "491848c7-55dc-4584", "", "3bda06f6-875d-4f05", "", "Functional Group", "f1b1694a-270d-4aed", "", "88bc65c8-2d2b-4545", "", "Type Compound", "b4ea30e9-e59e-4a4e", "", "dfba9cb8-74f8-4dc5", "", "Example", "9801422a-5e06-46ec", "", "5b130e50-f7cb-468a", "", "IUPAC Name", "4dae441c-de52-4b93", "", "d5d3197f-b1c1-4fa0", "", "Common Name", "354472be-60eb-4c77", "", "cfd9ac9b-c72f-40fc", "", "970a8060-60d2-4f93", "", "C=C", "4ec3f3f0-f658-479b", "", "double bond", "c569f82e-c8fd-4958", "", "alkene", "e2ea7f3c-8b21-4154", "", "b445b680-df2e-4ca8", "", "C=CH", "f6b0d8a2-20ac-4913", "", "229b6cbd-f1ce-4cf2", "", "ethene", "efb5d610-ce28-4675", "", "ethylene", "57ef0341-8f07-48e1", "", "a0466ebc-d6d7-4b82", "", "ea539316-d28a-4dd2", "", "\u2261", "c40ea973-5526-4912", "", "triple bond", "52df2ffc-a9d2-4326", "", "alkyne", "bbddda8b-e927-4d1f", "", "HC", "f1736625-cbab-4c1d", "", "525507e4-e683-4a28", "", "ethyne", "bfac5f92-9cbd-462b", "", "acetylene", "9daeca9b-49e1-4e46", "", "1082431a-a0b5-4d86", "", "e7897bdc-1ba2-4080", "", "OH", "184748b3-f8e3-4393", "", "hydroxyl", "2cb6f83d-6dfd-468e", "", "alcohol", "155fd28e-06f8-4f8b", "", "2830f6d6-1bd2-475b", "", "d9ee3a1d-f1fc-492a", "", "methanol", "1004f650-3830-41ea", "", "5f71db4f-449d-4104", "", "1589dab1-231d-4dd2", "", "c80c4986-70ff-4569", "", "b12ea10d-e664-4802", "", "O", "a96908e0-6e56-4924", "", "63b29f3e-277c-481d", "", "oxy", "8e363156-e556-4dde", "", "ether", "ee70e1ee-ecac-4920", "", "34c1fdd4-89eb-4970", "", "COCH", "1b05e8e5-22bc-4797", "", "67f5517d-c667-4609", "", "methoxymethane", "118566ab-28f3-4687", "", "methyl ether", "0588417a-d589-4638", "", "7c13b3cc-1760-4406", "", "4c1daabb-c2b4-459a", "", "carbonyl", "2763a426-558e-4b36", "", "e975891c-6852-4454", "", "b1e38566-ce35-430d", "", "C=0", "b9d2da61-3efc-4a82", "", "methanal", "579f6c7b-4d9d-49c2", "", "formaldehyde", "625ef305-5fb2-4f86", "", "61f251c5-18e1-4720", "", "d1a61a42-f74b-4868", "", "cb7fb6ab-3670-4b3d", "", "c202b932-31e9-43e2", "", "02c7b131-f3e2-495d", "", "0ec6bbf5-46db-41d2", "", "3137ed68-5374-4519", "", "propanone", "76ec38aa-049e-408b", "", "acetone", "2101f78d-2aeb-4099", "", "0b7594bd-70a8-4046", "", "e36ecf3f-076f-40db", "", "carboxyl", "50b62896-6aa7-4753", "", "6b69b534-0722-4b1b", "", "HCOOH", "dd9443ba-bc45-4874", "", "/science-and-technology/chemistry/organic-chemistry/methanoic-acid", "a9c49f57-a115-479b", "", "methanoic acid", "c7c6364b-d2b5-42c6", "", "/science-and-technology/chemistry/organic-chemistry/formic-acid", "fc541d44-9f98-4d47", "", "formic acid", "9a95d788-30c0-427b", "", "d1a95ee9-3bab-473f", "", "5da58f75-7deb-4ba9", "", "a755b6c8-231f-41b3", "", "aea5cce5-28ed-453e", "", "HCOOCH", "0563ba23-eb8b-4c01", "", "d142e1d1-e701-49d1", "", "6573105e-a3d7-4250", "", "ethyl methanoate", "f8f01739-dc39-42eb", "", "ethyl formate", "45259f1c-98f3-4531", "", "f597d895-eb86-48ff", "", "1e43d748-540d-453d", "", "NH", "31e97d37-1722-4941", "", "8782ebe3-3750-4fec", "", "amino", "90dcdc9d-9709-49ed", "", "amine", "fd75e2dd-f379-4ebc", "", "d94f2c66-34a4-40e9", "", "6c8eba3f-c60b-422d", "", "47f68cef-55c6-4aaa", "", "aminomethane", "52542a00-3814-4a54", "", "methylamine", "839e0cc5-087f-43aa", "", "740f401a-29b2-4591", "", "774b039b-fb1d-46b7", "", "CN", "78ee9b85-5579-4921", "", "cyano", "03b51a2c-2207-4a29", "", "nitrile", "8bd668ce-a1db-4813", "", "a2606e61-872a-4b7a", "", "39820846-0784-4712", "", "ethanenitrile", "5941b732-09c6-4b0a", "", "acetonitrile", "b1b6c946-bc86-44f0", "", "a454b449-6b74-4d7c", "", "a1ed5476-4f4a-422d", "", "X", "bd6545a4-f9fe-4291", "", "c31f0229-7481-42aa", "", "haloalkane", "59d065c3-647c-4ab0", "", "447547a0-b255-4375", "", "Cl", "12950443-71a7-4860", "", "chloromethane", "7b6d8828-1c89-4865", "", "methyl chloride", "8fedf4b1-016b-420c", "", "of solvent. Of course, not all organic reactions are highly successful. One reaction might be a very simple one giving essentially 100 percent of the desired product; but another might be a complex multistep process yielding less than 5 percent overall of the wanted product.", "9f4f92bd-4e19-476f", "", "Organic reactions can often give remarkable control as to what products should be formed. Adding water to propene for example, produces 2-propanol in the presence of acid, but it yields 1-propanol if treated first with B", "94367404-5f2b-450d", "", "b61e84ae-d097-4717", "", " and then H", "836ea6a6-809f-410c", "", "72724320-059c-46cb", "", " in the presence of base.", "4ef638df-6ac9-4a3b", "", "Future Sources of Organic Chemicals", "0455bf2e-a9eb-447f", "", "/science-and-technology/technology/technology-terms-and-concepts/fossil-fuels", "2882d179-8211-4a1a", "", "Fossil fuels", " have been our primary natural source for many organic chemicals for more than a century, but our fossil fuel resources are finite, and they are being rapidly depleted (especially oil and gas). What will be our sources of organic materials in the future? Since fossil fuels are nonrenewable resources, it is believed that the twenty-first century will see a shift toward greater dependence on renewable raw materials. The largest U.S. chemical company has a goal of becoming 25 percent based on renewable resources by 2010. It is already producing 1,3-propanediol from cornstarch using a gene-tailored ", "e1b2bce7-1aa3-42dc", "", "E. coli", " bacterium. This diol is used in Du Pont's fiber Sorona, which is said to combine the best features of both polyester and nylon fibers. Succinic acid and polyhydroxybutyrate are also obtainable from renewable crops, and the list of such renewable raw materials is destined to grow. For example, ethylene (or ethene), CH", "a36177ef-9f77-4ff9", "", "=CH", "08be8f79-1f16-435f", "", ", which is a highly important commercial chemical used in making many industrial chemicals and polymers, is presently made by steam cracking of ethane obtained from oil or natural gas; but ethylene can also be made by dehydration of ethyl alcohol made by fermentation of sugar. Efforts are even being made to use biowaste materials, such as corn husks, nutshells, and wood chips as industrial raw materials.", "aa37347a-b647-46f5", "", "Analytical Tools", "d8d63793-5c73-417c", "", "Organic chemists often need to examine products for identification, purity analysis, or structure determination. There are some marvelous tools available to help them do these things. ", "440c294b-7130-4a5b", "", "Chromatography", " , ", "b68241c5-0919-46eb", "", "spectroscopy", " , and crystallography are especially widely used in organic chemistry.", "c7f87fc8-02c4-416c", "", "Column chromatography, gas chromatography, and liquid chromatography are all important methods for separating mixtures of organic compounds. Spectroscopic tools include ultraviolet (UV), infrared (IR), nuclear ", "/science-and-technology/physics/physics/magnetic-resonance", "ff942541-b470-4958", "", "magnetic resonance", " (NMR), and mass spectroscopy (MS), each capable of providing a different kind of information about an organic compound. Although it is limited to substances that can be prepared as pure crystals, x-ray crystallography is probably the ultimate tool for determining molecular structure.", "21dbd70a-f9b3-4da4", "", "Careers in Organic Chemistry", "27e24360-b137-44a9", "", "Some organic chemists are involved in basic research at government or academic institutions, but most have careers in industry. The industries vary from oil and chemical companies to industries producing food, pharmaceuticals, cosmetics, detergents, paints, plastics, pesticides, textiles, or other kinds of products. Many organic chemists work in laboratories, where they do various kinds of analysis or research, but many others do not. Some are teachers, or writers, or science librarians. Some study law and become patent attorneys; some study medicine and become medical researchers; and some study business and become administrators of companies, colleges, or other institutions. Organic chemistry is an enormous field full of many kinds of career possibilities.", "6b2f49df-1764-4ce6", "", "see also Fossil Fuels; Lavoisier, Antoine; Organic Halogen Compounds; W", "5eb3b1fb-cc24-48b0", "", "\u00d6", "hler, Friedrich.", "1aa2fd59-aa02-418b", "", "ea61533b-2bfa-4c4a", "", "Kenneth E. Kolb", "e24cfdb6-0555-4786", "", "Bibliography", "81eb7a96-dea1-46ee", "", "Atkins, Robert C., and Carey, Francis A. (2002). ", "558277f7-8dc5-4de1", "", "Organic Chemistry: A Brief Course,", " 3rd edition. Boston: McGraw-Hill.", "931089a5-ebe8-42e2", "", "Bailey, Philip S., Jr., and Bailey, Christina A. (2000). ", "516257f1-c702-4f32", "", "Organic Chemistry: A Brief Survey of Concepts and Applications,", " 6th edition. Upper Saddle River, NJ: Prentice Hall.", "82a3b836-0f4c-4153", "", "Brown, William H., and Foote, Christopher S. (2002). ", "917902bc-aa35-4144", "", "Organic Chemistry,", " 3rd edition. ", "/places/united-states-and-canada/us-political-geography/san-diego", "eb93600b-7588-4e82", "", "San Diego", ": Saunders.", "2ae27909-6c95-43bd", "", "Fessenden, Ralph J.; Fessenden, Joan S.; and Logue, Marshall (1998). ", "919a5ac2-7870-4ba4", "", " 6th edition. Pacific Grove, CA: Brooks/Cole.", "de44aac1-96cb-4217", "", "Solomons, T. W. Graham (1997). ", "a0586a7e-251f-461d", "", "Fundamentals of Organic Chemistry,", " 5th edition. ", "092e79fa-8614-482c", "", ": Wiley.", "530c22cb-58fe-4028", "", "375781e7-9bf5-4441", "", "Chemistry: Foundations and Applications", "ed28bc7d-1590-41a1", "", "Kolb, Kenneth E.", "citationModal1", "8d9f0ece-40cb-4e99", "", "f659095f-8732-4604", "", "183a8c91-0e77-4880", "", "eaacc43d-222e-4154", "", "37a79c8b-5ddf-4ef2", "", "0bafc4bb-e9ce-47d4", "", "cfd209c1-82dd-4c67", "", "de23900c-446d-4674", "", "60f74c77-111d-445d", "", "8c0e3d22-2d04-463a", "", "445cd43b-cae6-44d9", "", "53cb71e5-6b75-4c7f", "", "df977e6e-3f26-40f4", "", "e2eb2eff-7ed8-45c0", "", "bca4820a-4ce9-4df8", "", "5a5e4b82-3555-4593", "", "4ade2095-cc97-48ff", "", "#mlaTab1", "bafdc145-b697-4fed", "", "3229a481-c91d-4f3f", "", "#chicagoTab1", "844e67f8-0b98-4275", "", "072a58ed-9ce4-4b3f", "", "#apaTab1", "f64f4d6b-0ce3-4aa4", "", "a8266eff-b47b-4232", "", "mlaTab1", "53c6f1fe-6078-4309", "", "be74a020-9c66-4303", "", " Kolb, Kenneth E. \"", "/science/news-wires-white-papers-and-books/organic-chemistry\n", "2d11b63c-a9d7-47ca", "", "0267f870-52d0-4b7a", "", "e29bb9ac-faf9-4a66", "", "bc671d32-61c3-4f96", "", "e0f28e1e-9a97-40e9", "", "4e3685e4-a09d-4025", "", "chicagoTab1", "04597958-d8ad-4a1c", "", "3fd922b9-00c0-4dc5", "", " Kolb, Kenneth E. \"Organic Chemistry\n.\" ", "03eb590a-dbdb-448c", "", "50f991b5-3b16-4541", "", "c6524970-d53d-464e", "", "https://www.encyclopedia.com/science/news-wires-white-papers-and-books/organic-chemistry", "apaTab1", "19ec2a1e-9584-401e", "", "b8e2e260-c9c6-4461", "", "2b0d476a-3902-4e8e", "", "982e9993-e529-4ffb", "", " https://www.encyclopedia.com/science/news-wires-white-papers-and-books/organic-chemistry", "7102574c-54f1-4eba", "", "#learnCitation1", "learnCitation1", "0027c69f-3cc1-4efa", "", "f9eb7b8d-80ca-421f", "", "aee3ffa6-f0ff-49b8", "", "a3474061-1834-4076", "", "a8b580e2-096b-4951", "", "ab48aaca-5e82-4762", "", "b64f8901-40e6-4465", "", "d3786e22-6da5-45ad", "", "9262a45b-e5dc-48d6", "", "1173e95a-407a-4d90", "", "89eb463d-b098-42a3", "", "0ced24c2-2364-4c6f", "", "62abae40-6686-4623", "", "4cfd935d-6859-41b5", "", "4f1a6bc8-fbc5-4938", "", "50edfa70-4576-47a7", "", "c3da59b9-578d-4b73", "", "ad53fa87-7238-4ef1", "", "d66fadbd-f85b-4cd1", "", "caf2ef22-3581-4957", "", "21b52f5d-2a56-4604", "", "b5347d4a-5212-408d", "", "333fe21b-e32a-4b34", "", "1c3a4d38-1878-486f", "", "36af94ff-f0aa-4c4a", "", "f6b273fb-8126-4edf", "", "articleWrapper-955204", "2f338ea9-e1c3-4a2c", "", "1G23438100472", "6375f17c-107c-4135", "", "#collapseExample2", "multiCollapseExample2", "de2aad05-c5b7-403b", "", "93a69c45-8d13-4601", "", "8953cdb2-4fbf-4782", "", "f18f6f7f-d59f-4e3d", "", "78a59784-eb6d-4786", "", "47f9c07b-4c9c-485c", "", "d9ba7cd5-69a1-445b", "", "1,337,339", "c8a4f13f-9011-4bba", "", "7509a1dd-66a8-4745", "", "May 18 2018", "a3ef70b3-5168-4bd1", "", "e4c7dc1b-3087-43b5", "", "82f3c068-a60c-4467", "", "1ed603fb-72d1-4024", "", "2540f0a2-0536-4bfa", "", "cebd38ab-e690-4c25", "", "#citationModal2", "10467f8a-6e16-41fc", "", "1c354628-81ad-447b", "", "8ff4e1ea-4cc8-4421", "", "bb1d8e66-6f88-4853", "", "8969fcf3-b727-4e25", "", "453d5984-17b0-4af8", "", "cbca2485-c990-406a", "", "collapseExample2", "0b801ed7-7251-42d2", "", "1c5a81de-a6de-4264", "", "Organic chemistry", "738c9694-1b75-4882", "", "Organic chemistry is the study of compounds of carbon. The name organic goes back to a much earlier time in history when chemists thought that chemical compounds in living organisms were fundamentally different from those that occur in nonliving things. The belief was that the chemicals that could be extracted from or that were produced by living organisms had a special \"vitalism\" or \"breath of life\" given to them by some supernatural being. As such, they presented fundamentally different kinds of problems than did the chemicals found in rocks, minerals, water, air, and other nonliving entities. The chemical compounds associated with living organisms were given the name organic to emphasize their connection with life.", "6b947d95-27b2-4f9c", "", "In 1828, German chemist Friedrich W", "6df5323e-b111-4020", "", "928db81a-3c1c-4511", "", "a842b4c0-2564-4378", "", "4adaa5c9-2d0b-47fd", "", "hler (1800", "5cb07251-1622-43b1", "", "2a40d43f-9b64-4231", "", "9da3e71a-f6d1-4fb3", "", "17220771-7d71-4b49", "", "1882) proved that this theory of vitalism was untrue. He found a very simple way to convert chemical compounds from living organisms into comparable compounds from nonliving entities.", "7ebc7a44-6bb4-4370", "", "As a result of W", "bbe0a57c-ae96-47c1", "", "4e0db373-92b8-419e", "", "4954048a-6e57-4995", "", "163a66ac-5b3a-471b", "", "hler's research, the definition of ", "9f33809d-f705-489b", "", " changed. The new definition was based on the observation that every compound discovered in living organisms had one property in common: they all contained the element carbon. As a result, the modern definition of ", "42b9bc06-3386-4674", "", "446a7cf7-fc76-418a", "", "ee401ab4-826d-41a5", "", "47b642e5-897d-4117", "", "83255bf9-073e-4915", "", "as the study of carbon compounds", "7215ce5b-704d-45cf", "", "cdd4fe73-acab-4d8b", "", "a74ab5b6-2927-4cce", "", "312cda9e-e293-4849", "", "was adopted.", "3fd0d91f-92fd-4add", "", "Organic and ", "/science-and-technology/chemistry/chemistry-general/inorganic-chemistry", "c89ba844-8e36-4823", "", "inorganic chemistry", "8dc1e95d-1ce3-4483", "", "One important point that W", "4802de77-77f0-4964", "", "e6232d80-2c60-40a9", "", "5b1f1e31-a1dd-421c", "", "23bbb123-d50f-484a", "", "hler's research showed was that the principles and techniques of chemistry apply equally well to compounds found in living organisms and in nonliving things. Nonetheless, some important differences between organic and inorganic (not organic) compounds exist. These include the following:", "6bcbff12-656a-4ef7", "", "Major Organic Families and the Functional Groups They Contain", "1bc94f7a-ad47-476b", "", "a0d213bd-e64f-4b2c", "", "53edbc23-6d18-4aab", "", "bcd64354-664c-40b7", "", "85d7ff38-2391-4b6f", "", "Family", "d3c44cf0-b10a-468d", "", "58921693-d623-4f6d", "", "b4555294-f6e1-40ed", "", "6c5ca97e-7fd0-4089", "", "dfb8120c-5cea-461f", "", "Alkane", "449be1c5-a90e-4326", "", "carbon-carbon singal bonds only: C-C", "1bff605b-673e-4f5e", "", "942806b4-cf72-4964", "", "Alkene", "12afd427-a376-45a0", "", "at least one carbon-carbon double bond: C=C", "a6c264d8-d5cd-4ed8", "", "7fdaa149-f66e-4c4c", "", "Alkyne", "5ec05a4d-a107-4567", "", "at least one carbon-carbon triple bond: C", "b15fcd17-efe2-41cc", "", "95a1dadb-00b7-4333", "", "dfff05f1-e2f8-4314", "", "9e6b04c4-30e8-4343", "", "989fb973-47fb-46fe", "", "c6ecaab3-b29f-4e9a", "", "Alcohol", "41bcddc2-1926-4fd8", "", "/science-and-technology/chemistry/organic-chemistry/hydroxyl-group", "82746792-ac1a-44d5", "", "hydroxyl group", ": C-OH", "417f9ffa-4a48-4644", "", "2455343c-eb29-406b", "", "Ether", "1ec31e91-2093-4171", "", "carbon-oxygen-carbon bonding: C-O-C", "ab0b2b57-d566-428b", "", "87888e29-1253-498a", "", "Aldehyde and ketone", "a9943c73-f55e-4f86", "", "carboxyl (C=O) group: C-C=O", "85a0427a-ed16-480f", "", "4f911336-bfd4-4793", "", "Carboxylic acid", "ea1f3f93-251d-469c", "", "carboxylic (C=O) group:", "a6b49a4d-1777-4080", "", "96157f2f-c388-4025", "", "Ester", "ed6c110d-cf28-4346", "", "ester (C=O) group:", "ecd02bc7-6973-4848", "", "1935f4d1-13ed-4d4a", "", "Amine", "a9646c2e-5b92-4b9b", "", "amine (NH", "1f0ebc21-dd29-4268", "", ") group: C-NH", "86faa806-b767-4540", "", "b1f45d3a-5dfa-4af2", "", "1. The number of organic compounds vastly exceeds the number of inorganic compounds. The ratio of carbon-based compounds to non-carbon-based compounds is at least ten to one, with close to 10 million organic compounds known today. The reason for this dramatic difference is a special property of the carbon atom: its ability to join with other carbon atoms in very long chains, in rings, and in other kinds of geometric arrangements. It is not at all unusual for dozens, hundreds, or thousands of carbon atoms to bond to each other within a single compound", "9ce32fd4-ace3-4b85", "", "41089788-83b1-48ce", "", "9aa4da49-0164-4675", "", "ce560c49-82ee-4652", "", "a property that no other element exhibits.", "1eb279a2-2264-41f3", "", "2. In general, organic compounds tend to have much lower melting and boiling points than do inorganic compounds.", "d01ea02d-d0f7-4a16", "", "3. In general, organic compounds are less likely to dissolve in water than are inorganic compounds.", "462a6c0f-2b98-459d", "", "4. Organic compounds are likely to be more flammable but poorer conductors of heat and electricity than are inorganic compounds.", "d3ea3256-6bf0-4d87", "", "5. Organic reactions tend to take place more slowly and to produce a much more complex set of products than do inorganic reactions.", "8adb7773-4747-4749", "", "Functional groups and organic families", "0a460894-0511-4c54", "", "The huge number of organic compounds requires that some system be developed for organizing them. The criterion on which those compounds are organized is the presence of various functional groups. A functional group is an arrangement of atoms that is responsible for certain characteristic physical and chemical properties in a compound. For example, one such functional group is the ", "98554927-6781-4df3", "", ", consisting of an oxygen atom and hydrogen atom joined to each other. 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span {white-space: normal;}#final_closed_panel\"+M(v)+\" #final_closed_text.visible {opacity: 1;}\"+(m?\"#personalize_toggle\"+M(v)+\" {pointer-events: none; margin-top: 6px; margin-bottom: 6px;}#ad_options_panel\"+M(v)+\" span {display: block; text-align: center; line-height: 1em;}\":\"\")+\".fallback-wrap .btn{margin: 1px auto 1px auto; white-space: normal;}.close {\"+(a?\"left: 5%;\":\"top: 2px; left: 2px;\")+\"display: inline-block; position: absolute; color: black; font-size: 15px; line-height: 15px; opacity: 0.5; height: 15px; width: 15px; user-select: none; cursor: pointer;}\"+\n(a?\".panel-buttons {position: relative;}\":\"\")+'[dir=\"rtl\"] .close {right: 2px; transform: scaleX(-1);}[dir=\"rtl\"] #menu-dismiss'+M(v)+\" {left: initial; right: 0; transform: scaleX(-1);}.native-arrow {\"+(n?\"opacity: 0.6;\":\"opacity: 0.8;\")+\"}.window-icon {opacity: 0.4;}\"+(n?\"#native-menu-bg\"+M(v)+\" {position: absolute; top: 0; left: 0; display: inline-block; width: 100%; height: 100%; background-color: rgba(0,0,0,0.6); cursor: pointer;}.native-panel-wrapper {display: inline-block; padding: 0.1em;}.visible .native-panel {margin-top: 0; opacity: 1;}#menu-dismiss\"+\nM(v)+\" {position: absolute; top: 0; left: 0; cursor: pointer;}#menu-dismiss\"+M(v)+\" svg {height: 1.4em; width: 1.4em; max-height: 24px; max-width: 24px; min-height: 10px; min-width: 10px;}.cross {opacity: 0.6; stroke: #52b4c6; stroke-width: 1.25; transform: rotate(0deg); transform-origin: 50% 50%; transition: opacity 0.1s linear, transform 0.1s linear;}#menu-dismiss\"+M(v)+\":hover .cross {opacity: 0.9; transform: rotate(90deg);}.native-panel-contents {display: flex; flex-wrap: nowrap; flex-direction: column; margin: 0.8em;}.header {display: flex; flex-direction: row; justify-content: flex-start; white-space: nowrap; font-size: 1.3em;}.header-text-wrapper {display: inline-block; margin: 0 0 0.2em 0.1em;}.header {margin: 0 0 5px 0;}#menu-dismiss\"+\nM(v)+\" svg {height: 1em; width: 1em; margin: 0.1em;}.cross {stroke: #888;}.header-text-wrapper {margin: 0 0 0.4em 0;}.native-panel-wrapper {display: flex; padding: 0; justify-content: center; align-items: center; height: 100%;}#native_closed_text\"+M(v)+\" img {margin: 0 0.3em -0.1em 0.3em;}.header {font-size: 1em; justify-content: center}.native-panel {opacity: 0; display: inline-block; position: relative; box-sizing: border-box; color: rgba(0,0,0,0.4); background-color: #fafafa; font-family: 'Arial', sans-serif; white-space: nowrap; border-radius: 4px; box-shadow: 0 3px 2px 0 rgba(0,0,0,0.3); margin-top: 5px; transition: margin 0.25s ease-out;}.native-button-container {display: flex; justify-content: center; flex-wrap: nowrap; flex-direction: column;}.native-button-container #report_btn\"+\nM(v)+\" {color: white; background-color: rgba(26,115,232,1); border: 1px solid rgba(66,133,245,0.6); opacity: 0.9;}.native-button-container #report_btn\"+M(v)+\":hover {background-color: rgba(20,91,183,1);}.native-button-container #settings_btn\"+M(v)+\", .native-button-container #why_this_ad_btn\"+M(v)+\", .native-button-container #learn_more_btn\"+M(v)+\" {color: rgba(0,0,0,0.5); border: 1px solid rgba(0,0,0,0.3);}.native-button-container a {display: flex; flex-direction: row; justify-content: center; align-items: center; margin: 5px 0 0 0; flex-grow: 1; cursor: pointer; border-radius: 4px; box-shadow: 0 0 2px rgba(0,0,0,0.12), 0 1px 3px rgba(0,0,0,0.26) !important; background-color: white; font-size: 0.8em; line-height: 1em;}.native-button-container a:hover {background-color: #f5f5f5;}.native-button-container a, .native-button-container a:active, .native-button-container a:hover, .native-button-container a:visited {text-decoration: none;}.native-button-container a:first-child {margin-top: 0;}.button-text {font-size: 1em; display: block;}.padded-text {margin: 0.4em 0.7em;}.native-button-container #settings_icon {opacity: 0.65; opacity: 0.65;}.icon {display: inline-block; width: 2.3em; height: 2.3em; fill: #fff; stroke: none; margin: 0.2em;}\"+\n(.5>=g/h?\".native-panel-wrapper {padding-top: 1em; align-items: flex-start;}\":\"\")+(2<=g/h&&100>=h?\".native-panel-contents {margin: 0.5em;}.native-button-container a {margin: 0 0 0 0.2em;}.header {margin: 0;}.native-button-container a:first-child {margin: 0;}.native-panel-contents {flex-direction: column;}.native-button-container {flex-direction: row;}\":\"\")+(3<=g/h&&49>=h?\".native-panel-contents {margin: 0.5em 1em;}.native-panel {margin: 0.1em;}.header {margin: 0 0.2em 0 0;}.native-panel-contents {flex-direction: row;}.native-button-container {flex-direction: row;}.header-text-wrapper {margin-bottom: 0;}\":\n\"\")+(130>=h?\".padded-text {white-space: normal; margin: 0.3em; text-align: initial;}\":\"\"):\"\")+(f?\"#panel_set\"+M(v)+\" .panel-content {font-family: 'Google Sans', sans-serif;}#closed_text\"+M(v)+\" img, #native_closed_text\"+M(v)+\" img, #final_closed_text\"+M(v)+' img {margin: 0 0 -0.3em 0; height: 1.1em; min-width: 3.3em;}.close {top: 6px; left: 6px; height: 22px; width: 22px;}[dir=\"rtl\"] .close {right: 8px; transform: scaleX(-1);}.btn>span {padding: 0.7em 0.5em;}#ad_closed_panel'+M(v)+\" .btn, #ad_options_panel\"+\nM(v)+\" .btn {border-radius: 4px;}#ad_closed_panel\"+M(v)+\" .settings-btn, #ad_options_panel\"+M(v)+\" .settings-btn {box-shadow: inset 0 0 0 1px #dadce0;}#closed_text\"+M(v)+\", #final_closed_text\"+M(v)+' {line-height: 1.28em; font-size: 1.15em;}.btn-icon {margin-right: 0.5em;}[dir=\"rtl\"] .btn-icon {float: none;}'+(2<=g/h?\".spacer\"+M(v)+\" {width: 4px;}#closed_text\"+M(v)+\", #final_closed_text\"+M(v)+\" {line-height: 1em;}\"+(90<=h?\".close {height: 24px; width: 24px; top: 8px; left: 8px;}#closed_text\"+M(v)+\n\", #final_closed_text\"+M(v)+\" {font-size: 1.3em;}.panel-lower {margin-top: 6px;}.panel-buttons {margin-top: 6px;}\":\"#closed_text\"+M(v)+\", #final_closed_text\"+M(v)+\" {font-size: 1.1em;}.close {height: 20px; width: 20px;}.panel-lower {margin-top: 2px;}.panel-buttons {margin-top: -2px;}.btn > span {padding: 0.4em;}\"):200>=g?\".panel-lower {margin-top: 25px;}.close {height: 16px; width: 16px;}\":\".panel-lower {margin-top: 40px;}.panel-buttons {margin-top: 14px;}#panel_set\"+M(v)+\" .panel-row:first-child {padding: 0 17px;}#ad_closed_panel\"+\nM(v)+\" .responsive-btn, #ad_options_panel\"+M(v)+\" .responsive-btn {margin-bottom: 8px; width: 51%;}\"):\"#panel_set\"+M(v)+\" .panel-content {font-family: 'Arial', sans-serif;}#ad_closed_panel\"+M(v)+\" .btn, #ad_options_panel\"+M(v)+\" .btn {border-radius: 2px; box-shadow: 0 0 2px rgba(0,0,0,0.12), 0 1px 3px rgba(0,0,0,0.26) !important;}\")+(m?\"#learn_more_btn\"+M(v)+\" .window-icon {height: 16px; width: 16px;}#personalize_toggle\"+M(v)+\" .track {pointer-events: all; position: relative; display: inline-block; width: 36px; height: 14px; top: 1px; margin-left: 6px;}#personalize_toggle\"+\nM(v)+\" .track input {opacity: 0; width: 0; height: 0;}#personalize_toggle\"+M(v)+\" .handle {position: absolute; cursor: pointer; top: 0; left: 0; right: 0; bottom: 0; background-color: #dadce0; -webkit-transition: .4s; transition: .4s; border-radius: 7px;}#personalize_toggle\"+M(v)+' .handle:before {position: absolute; content: \"\"; height: 20px; width: 20px; left: -4px; bottom: -3px; margin-left: 4px; background-color: #fff; -webkit-transition: .4s; transition: .4s; box-shadow: 0 1px 2px 0 rgba(60, 64, 67, .3), 0 1px 3px 1px rgba(60, 64, 67, .15); border-radius: 50%;}#personalize_toggle'+\nM(v)+\" input:checked + .handle {background-color: rgba(66, 133, 244, .5);}#personalize_toggle\"+M(v)+\" input:focus + .handle {box-shadow: 0 0 1px #4285f4;}#personalize_toggle\"+M(v)+\" input:checked + .handle:before {-webkit-transform: translateX(16px); -ms-transform: translateX(16px); transform: translateX(16px); transition: .4s; -webkit-transition: background-color .4s; -ms-transition: background-color .4s; transition: background-color .4s; background-color: #1a73e8;}\"+(200>=g||200>=h?\"#personalize_toggle\"+\nM(v)+\" .track {width: 24px; height: 9px; top: 2px;}#personalize_toggle\"+M(v)+\" .handle:before {height: 13px; width: 13px; left: -7px; bottom: -2px;}#learn_more_btn\"+M(v)+\" .window-icon {height: 14px; width: 14px;}\":\"\")+(500<=h?\"#personalize_toggle\"+M(v)+\" {margin-top: 6;}\":\"\")+(100>=g||100>=h?\"#personalize_toggle\"+M(v)+\" {margin-top: 0; margin-bottom: 3px;}#learn_more_btn\"+M(v)+\" .window-icon {height: 12px; width: 12px;}\":\"\")+(60>=g||60>=h?\"#learn_more_btn\"+M(v)+\" .window-icon {height: 11px; width: 11px;}\":\n\"\")+(50>=g||50>=h?\"#learn_more_btn\"+M(v)+\" .window-icon {height: 9px; width: 9px;}\":\"\"):\"\")+\"</style>\");return c(d+b)},fw=function(a){var b=a.creativeIndexSuffix;a=a.Ik;return Dv('<a id=\"ad_options_btn'+L(b)+'\" class=\"btn responsive-btn primary-btn shadow\"><span id=\"options_text'+L(b)+'\" class=\"btn-text\">'+Gv(a)+\"</span></a>\")},gw=function(a,b){return Dv('<img id=\"why_this_ad_icon'+L(a)+'\" class=\"btn-icon\" src=\"'+L(Vv(b))+'\" alt=\"\">')},ew=function(){return Dv('<svg viewBox=\"0 0 24 24\"><path class=\"native-arrow\" d=\"M20 11H7.83l5.59-5.59L12 4l-8 8 8 8 1.41-1.41L7.83 13H20v-2z\"/></svg>')},\nhw=function(){return Dv('<svg class=\"window-icon\" xmlns=\"http://www.w3.org/2000/svg\" viewBox=\"0 -2 24 24\"><path d=\"M0 0h24v24H0V0z\" fill=\"none\"/><path d=\"M19 19H5V5h7V3H5c-1.11 0-2 .9-2 2v14c0 1.1.89 2 2 2h14c1.1 0 2-.9 2-2v-7h-2v7zM14 3v2h3.59l-9.83 9.83 1.41 1.41L19 6.41V10h2V3h-7z\"/></svg>')};var jw=function(a,b){var c=a.creativeIndexSuffix,d=a.Hl,e=a.om,f=Dv,g=Hv({hl:d?\"left\":\"right\",Ok:d?\"right\":\"left\"},a);d=g.hl;var h=g.Ok,k=g.creativeIndexSuffix,m=g.Qk,n=g.Sk,p=g.Rk,r=g.xm,t=g.Xl,w=g.jh,z=g.Ih,I=g.fg,v=g.vg,T=g.Wh;g=g.Jf;b=b&&b.bl;b=\"&nbsp;\"+Dv((v?'<link href=\"https://fonts.googleapis.com/css?family=Google+Sans_old\" rel=\"stylesheet\"'+(b?' nonce=\"'+L($v(b))+'\"':\"\")+\">\":\"\")+\"<style\"+(b?' nonce=\"'+L($v(b))+'\"':\"\")+\">#survey-container\"+M(k)+\" {position: absolute; top: 0; left: 0;\"+(w?\n\"width: 100%; height: 100%;\":\"width: \"+M(z)+\"px; height: \"+M(I)+\"px;\")+\"overflow: hidden;\"+(g?\"display: table;\":\"\")+\"background-color: #fafafa; font-size: 0; white-space: nowrap;}.survey-native-scroll #survey-container\"+M(k)+\" {overflow-x: scroll;}.survey-horiz, .survey-vert {text-align: center;}#survey-container\"+M(k)+\" * {box-sizing: border-box; -moz-box-sizing: border-box; -webkit-box-sizing: border-box;}.survey-block {height: \"+M(m)+\"px;}.survey-option {position: relative; overflow: hidden; display: inline-block; padding: 1px 5px; width: \"+\nM(n)+\"px; height: \"+M(m)+\"px; border: 1px solid #e0e0e0; background-color: #fff; cursor: pointer;}.survey-option:hover, .survey-scroll .survey-option:active {background-color: #f5f5f5;}.survey-option div {width: 100%; height: 100%; display: table; text-align: center;}.survey-option span {vertical-align: middle; display: table-cell; color: #4285f4; font-family: Arial, sans-serif; text-align: center; font-size: 12px; line-height: 14px; white-space: normal;}@media (min-height: 54px) {.survey-horiz.survey-spaced .survey-option, .survey-vert .survey-option {box-shadow: 0 0 2px rgba(0,0,0,0.12), 0px 1px 3px rgba(0,0,0,0.26) !important; border: none;}}#mute_panel\"+\nM(k)+\".survey-horiz .survey-option {display: inline-block; margin-\"+M(h)+\": -1px; box-shadow: none;}#mute_panel\"+M(k)+\".survey-horiz .survey-option:first-child {margin-\"+M(h)+\": 0;}#mute_panel\"+M(k)+\".survey-horiz.survey-spaced .survey-option {margin-\"+M(h)+\": \"+M(p)+\"px;}#mute_panel\"+M(k)+\".survey-horiz.survey-spaced .survey-option:first-child {margin-\"+M(h)+\": 0;}#mute_panel\"+M(k)+\".survey-horiz.jake-middle .survey-block {margin-top: \"+M((I-m)/2)+\"px;}#mute_panel\"+M(k)+\".survey-horiz.jake-top .survey-block {margin-top: \"+\nM(p)+\"px;}#mute_panel\"+M(k)+\".survey-vert .survey-option, #mute_panel\"+M(k)+\".survey-horiz.survey-spaced .survey-option {border-radius: 2px;}#mute_panel\"+M(k)+\".survey-vert .survey-option {margin: \"+M(p)+\"px auto 0 auto; display: block;}#mute_panel\"+M(k)+\".survey-vert.jake-top .survey-option:first-child {margin-top: \"+M(p)+\"px;}#mute_panel\"+M(k)+\".survey-vert.jake-middle .survey-option:first-child {margin-top: \"+M((I-r)/2)+\"px;}#mute_panel\"+M(k)+\".survey-grid #survey-container\"+M(k)+\" {width: initial; height: initial; white-space: normal; padding: 1px;}#mute_panel\"+\nM(k)+\".survey-grid .survey-option {display: inline-block; width: \"+M((z-6)/2)+\"px; height: \"+M((I-6)/2)+\"px; margin: 1px;}#mute_panel\"+M(k)+\".survey-small-grid #survey-container\"+M(k)+\" {white-space: normal; padding: \"+M(I/2-(m+2))+\"px 0px;}#mute_panel\"+M(k)+\".survey-small-grid #option-container\"+M(k)+\" {padding: 0 \"+M(z/2-(n+2))+\"px;}#mute_panel\"+M(k)+\".survey-small-grid .survey-option {display: inline-block; margin: 1px;}.option-container {\"+(g?\"display: table-cell; vertical-align: middle;\":\"margin-top: \"+\nM(T)+\"px; display: inline-block;\")+\"}.scroll, .native-scroll {position: absolute; top: 0; display: none;}.scroll {width: 30px; border: 1px solid transparent; background-color: #666; background-color: rgba(0,0,0,0.6); text-align: center; transition: visibility 150ms step-end; cursor: pointer;}.native-scroll {width: 10px;}.survey-scroll .scroll, .survey-native-scroll .native-scroll {display: block;}.scroll div {position: absolute; top: 50%; left: 50%; height: 36px; width: 36px; margin: -18px 0 0 -18px;}.scroll:hover, .scroll:active {background-color: #999; background-color: rgba(0,0,0,0.4);}.scroll-right {\"+\nM(d)+\": 0;}.native-scroll.scroll-\"+M(d)+\" {-webkit-box-shadow: inset -10px 0 10px -10px rgba(0,0,0,0.3); -moz-box-shadow: inset -10px 0 10px -10px rgba(0,0,0,0.3); box-shadow: inset -10px 0 10px -10px rgba(0,0,0,0.3);}.scroll-right {border-top-\"+M(h)+\"-radius: 4px; border-bottom-\"+M(h)+'-radius: 4px;}.scroll-right div {background-image:url(\"'+Vv(t)+\"/images/icons/material/system/1x/keyboard_arrow_\"+Pv(d)+'_white_36dp.png\");}.scroll-left {'+M(h)+\": 0;}.native-scroll.scroll-\"+M(h)+\" {-webkit-box-shadow: inset 10px 0 10px -10px rgba(0,0,0,0.3); -moz-box-shadow: inset 10px 0 10px -10px rgba(0,0,0,0.3); box-shadow: inset 10px 0 10px -10px rgba(0,0,0,0.3);}.scroll-left {border-top-\"+\nM(d)+\"-radius: 4px; border-bottom-\"+M(d)+'-radius: 4px;}.scroll-left div {background-image:url(\"'+Vv(t)+\"/images/icons/material/system/1x/keyboard_arrow_\"+Pv(h)+'_white_36dp.png\");}.survey-option {transition: margin 150ms linear;}'+(v?\".survey-option {font-family: 'Google Sans', sans-serif; border-radius: 4px;}@media (min-height: 54px) {.survey-horiz.survey-spaced .survey-option, .survey-vert .survey-option {box-shadow: inset 0 0 0 1px #dadce0 !important; border: none;}}\":\"\")+\"</style>\")+'<div id=\"survey-container'+\nL(c)+'\"><div id=\"option-container'+L(c)+'\" class=\"option-container\">';e=Hv({options:e},a);a=e.options;e=e.creativeIndexSuffix;d=\"\";h=a.length;for(k=0;k<h;k++)d+='<a wp=\"1\" class=\"survey-block survey-option\"><div wp=\"0\"><span>'+Gv(a[k])+\"</span></div></a>\";d+='<a id=\"scroll-left'+L(e)+'\" class=\"survey-block scroll scroll-left\" style=\"visibility:hidden\"><div></div></a><a id=\"scroll-right'+L(e)+'\" class=\"survey-block scroll scroll-right\" style=\"visibility:visible\"><div></div></a>';a=Dv(d);return f(b+\na+'</div></div><a id=\"native-scroll-left'+L(c)+'\" class=\"survey-block native-scroll scroll-left\" style=\"visibility:hidden\"><div></div></a><a id=\"native-scroll-right'+L(c)+'\" class=\"survey-block native-scroll scroll-right\" style=\"visibility:visible\"><div></div></a>')};var lw=function(a,b,c,d,e,f,g,h,k,m,n,p,r){this.F=a;this.g=b;this.l=c;this.U=g;this.j=h;this.la=k;this.R=d;this.Ha=e;this.K=f;this.ia=n;this.fa=p;this.da=r;this.aa=void 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WV(b),y(d,self.crypto.subtle.sign({name:\"HMAC\",hash:{name:a.hash}},a.key,b),2);c=d.g;return d.return(new Uint8Array(c.slice(0,a.Rc)))})},cW=function(a,b,c){var d;return A(function(e){if(1==e.h)return WV(b),WV(c),y(e,bW(a,c),2);d=e.g;if(b.length!==d.length)var f=!1;else{for(var g=f=0;g<b.length;g++)f|=b[g]^d[g];f=0==f}return e.return(f)})};\nfunction dW(a,b,c){var d;return A(function(e){if(1==e.h){WV(b);if(!Number.isInteger(c))throw new Y(\"invalid tag size, must be an integer\");if(10>c)throw new Y(\"tag too short, must be at least \"+(10).toString()+\" bytes\");switch(a){case \"SHA-1\":if(20<c)throw new Y(\"tag too long, must not be larger than 20 bytes\");break;case \"SHA-256\":if(32<c)throw new Y(\"tag too long, must not be larger than 32 bytes\");break;case \"SHA-384\":if(48<c)throw new Y(\"tag too long, must not be larger than 48 bytes\");break;\ncase \"SHA-512\":if(64<c)throw new Y(\"tag too long, must not be larger than 64 bytes\");break;default:throw new Y(a+\" is not 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k.return(c.g.decrypt(d))})};\nfunction fW(a,b,c,d,e){var f,g;return A(function(h){if(1==h.h)return WV(a),WV(d),y(h,ZV(a,b),2);if(3!=h.h)return f=h.g,y(h,dW(c,d,e),3);g=h.g;return h.return(new eW(f,b,g,e))})};var gW=function(){};\ngW.prototype.Zd=function(a){if(a instanceof Uint8Array){try{var b=uU(a)}catch(e){throw new X(\"Could not parse the given Uint8Array as a serialized proto of type.googleapis.com/google.crypto.tink.AesCtrHmacAeadKey\");}if(!b||!F(b,pU,1)||!F(b,rU,2))throw new X(\"Could not parse the given Uint8Array as a serialized proto of type.googleapis.com/google.crypto.tink.AesCtrHmacAeadKey\");}else if(a instanceof tU)b=a;else throw new X(\"Expected AesCtrHmacAeadKeyFormat-proto\");var c=hW(F(b,pU,1));a=c.Mk;c=c.hf;\nvar d=new hU;d=Cj(d,1,0,0);a=Ij(d,2,a);c=QV(c);a=Dj(a,3,c);c=iW(F(b,rU,2));b=c.Al;c=c.zl;d=new lU;d=Cj(d,1,0,0);b=Ij(d,2,b);c=QV(c);b=Dj(b,3,c);c=new nU;a=Ij(c,2,a);return Ij(a,3,b)};\nvar hW=function(a){if(!a)throw new X(\"Invalid AES CTR HMAC key format: key format undefined\");var b=Qj(a,2);VV(b);a=F(a,fU,1);if(!a)throw new X(\"Invalid AES CTR HMAC key format: params undefined\");var c=Qj(a,1);if(12>c||16<c)throw new X(\"Invalid AES CTR HMAC key format: IV size is out of range: \"+c);return{Mk:a,hf:b,Kc:c}},iW=function(a){if(!a)throw new X(\"Invalid AES CTR HMAC key format: key format undefined\");var b=Qj(a,2);if(16>b)throw new X(\"Invalid AES CTR HMAC key format: HMAC key is too small: \"+\nQj(a,2));a=F(a,jU,1);if(!a)throw new X(\"Invalid AES CTR HMAC key format: params undefined\");var c=Qj(a,2);if(10>c)throw new X(\"Invalid HMAC params: tag size \"+c+\" is too small.\");if(!jW.has(Sj(a,1)))throw new X(\"Unknown hash type.\");if(c>jW.get(Sj(a,1)))throw new X(\"Invalid HMAC params: tag size \"+c+\" is out of range.\");switch(Sj(a,1)){case 1:var d=\"SHA-1\";break;case 3:d=\"SHA-256\";break;case 4:d=\"SHA-512\";break;default:d=\"UNKNOWN HASH\"}return{Al:a,zl:b,yl:d,Rc:c}},jW=new Map([[1,20],[3,32],[4,64]]),\nkW=function(){this.g=new gW};l=kW.prototype;\nl.xb=function(a,b){var c,d,e,f,g,h=this,k,m,n,p,r,t;return A(function(w){if(1==w.h){if(a!=h.Oa())throw new X(\"Requested primitive type which is not supported by this key manager.\");if(b instanceof YU){if(!h.Nd(Rj(b,1)))throw new X(\"Key type \"+Rj(b,1)+\" is not supported. This key manager supports \"+h.Ua()+\".\");try{k=oU(Aj(b,2))}catch(T){throw new X(\"Could not parse the key in key data as a serialized proto of type.googleapis.com/google.crypto.tink.AesCtrHmacAeadKey\");}if(null===k||void 0===k)throw new X(\"Could not parse the key in key data as a serialized proto of type.googleapis.com/google.crypto.tink.AesCtrHmacAeadKey\");\n}else if(b instanceof nU)k=b;else throw new X(\"Given key type is not supported. This key manager supports \"+h.Ua()+\".\");var z=F(k,hU,2);if(!z)throw new X(\"Invalid AES CTR HMAC key format: key undefined\");XV(z.getVersion(),h.getVersion());var I=new pU;var v=F(z,fU,2);I=Ij(I,1,v);v=lV(Aj(z,3));I=Cj(I,2,v,0);I=hW(I).Kc;f=kV(Aj(z,3));g=I;m=f;n=g;z=F(k,lU,3);if(!z)throw new X(\"Invalid AES CTR HMAC key format: key undefined\");XV(z.getVersion(),h.getVersion());I=new rU;v=F(z,jU,2);I=Ij(I,1,v);v=lV(Aj(z,\n3));I=Cj(I,2,v,0);v=iW(I);I=v.yl;v=v.Rc;c=kV(Aj(z,3));d=I;e=v;p=c;r=d;t=e;return y(w,fW(m,n,r,p,t),2)}return w.return(w.g)})};l.Nd=function(a){return a===this.Ua()};l.Ua=function(){return\"type.googleapis.com/google.crypto.tink.AesCtrHmacAeadKey\"};l.Oa=function(){return TV};l.getVersion=function(){return 0};l.Pd=function(){return this.g};var lW=function(a){var b=a.vc;this.key=a.key;this.vc=b};lW.prototype.encrypt=function(a,b,c){var d=this,e,f;return A(function(g){if(1==g.h){if(12!==a.length)throw new X(\"IV must be 12 bytes\");e={name:\"AES-GCM\",iv:a,tagLength:128};c&&(e.additionalData=c);return y(g,self.crypto.subtle.encrypt(e,d.key,b),2)}f=g.g;return g.return(d.vc?mV(a,new Uint8Array(f)):new Uint8Array(f))})};\nlW.prototype.decrypt=function(a,b,c){var d=this,e,f,g,h,k;return A(function(m){if(1==m.h){e=d.vc?28:16;if(b.length<e)throw new X(\"ciphertext too short\");if(12!==a.length)throw new X(\"IV must be 12 bytes\");f={name:\"AES-GCM\",iv:a,tagLength:128};c&&(f.additionalData=c);g=d.vc?new Uint8Array(b.subarray(12)):b;m.j=2;h=Uint8Array;return y(m,self.crypto.subtle.decrypt(f,d.key,g),4)}if(2!=m.h)return m.return(new h(m.g));k=ua(m);throw new X(k.toString());})};\nfunction mW(a){var b=a.key,c=a.vc,d;return A(function(e){if(1==e.h){if(![16,32].includes(b.length))throw new Y(\"unsupported AES key size: ${n}\");return y(e,self.crypto.subtle.importKey(\"raw\",b,{name:\"AES-GCM\",length:b.length},!1,[\"encrypt\",\"decrypt\"]),2)}d=e.g;return e.return(new lW({key:d,vc:c}))})};var nW=function(a){this.key=a;this.g=new lW({key:a,vc:!0})};x(nW,TV);nW.prototype.encrypt=function(a,b){var c=this,d;return A(function(e){d=QV(12);return e.return(c.g.encrypt(d,a,b))})};nW.prototype.decrypt=function(a,b){var c=this,d;return A(function(e){d=new Uint8Array(12);d.set(a.subarray(0,12));return e.return(c.g.decrypt(d,a,b))})};\nfunction oW(a){var b;return A(function(c){if(1==c.h)return VV(a.length),y(c,self.crypto.subtle.importKey(\"raw\",a,{name:\"AES-GCM\",length:a.length},!1,[\"encrypt\",\"decrypt\"]),2);b=c.g;return c.return(new nW(b))})};var pW=function(){};\npW.prototype.Zd=function(a){if(a instanceof Uint8Array){try{var b=yU(a)}catch(c){throw new X(\"Could not parse the input as a serialized proto of type.googleapis.com/google.crypto.tink.AesGcmKey key format.\");}if(!Qj(b,2))throw new X(\"Could not parse the input as a serialized proto of type.googleapis.com/google.crypto.tink.AesGcmKey key format.\");a=b}else if(!(a instanceof xU))throw new X(\"Expected AesGcmKeyFormat-proto\");b=a;VV(Qj(b,2));a=new vU;b=QV(Qj(b,2));a=Dj(a,3,b);return Cj(a,1,0,0)};\nvar qW=function(){this.g=new pW};l=qW.prototype;\nl.xb=function(a,b){var c=this,d;return A(function(e){if(1==e.h){if(a!=c.Oa())throw new X(\"Requested primitive type which is not supported by this key manager.\");if(b instanceof YU){if(\"type.googleapis.com/google.crypto.tink.AesGcmKey\"!=Rj(b,1))throw new X(\"Key type \"+Rj(b,1)+\" is not supported. This key manager supports type.googleapis.com/google.crypto.tink.AesGcmKey.\");try{var f=wU(Aj(b,2))}catch(g){throw new X(\"Could not parse the input as a serialized proto of type.googleapis.com/google.crypto.tink.AesGcmKey key.\");}}else if(b instanceof\nvU)f=b;else throw new X(\"Key type is not supported. This key manager supports type.googleapis.com/google.crypto.tink.AesGcmKey.\");d=f;VV(lV(Aj(d,3)));XV(d.getVersion(),0);return y(e,oW(kV(Aj(d,3))),2)}return e.return(e.g)})};l.Nd=function(a){return a===this.Ua()};l.Ua=function(){return\"type.googleapis.com/google.crypto.tink.AesGcmKey\"};l.Oa=function(){return TV};l.getVersion=function(){return 0};l.Pd=function(){return this.g};var rW=function(){};var sW=function(a){this.g=a};x(sW,rW);sW.prototype.decrypt=function(a,b){var c=this,d,e,f,g,h;return A(function(k){switch(k.h){case 1:if(!a)throw new X(\"Ciphertext has to be non-null.\");if(!(5<a.length)){k.h=2;break}d=a.subarray(0,5);return y(k,jV(c.g,d),3);case 3:return e=k.g,f=a.subarray(5,a.length),k.j=4,y(k,tW(e,f,b),6);case 6:g=k.g;k.h=5;k.j=0;break;case 4:ua(k);case 5:if(g)return k.return(g);case 2:return y(k,jV(c.g,fV),7);case 7:return h=k.g,k.return(tW(h,a,b))}})};\nvar tW=function(a,b,c){var d,e,f,g;return A(function(h){switch(h.h){case 1:d=a.length,e=0;case 2:if(!(e<d)){h.h=4;break}if(1!=a[e].g){h.h=3;break}f=a[e].xb();g=void 0;h.j=5;return y(h,f.decrypt(b,c),7);case 7:g=h.g;h.h=6;h.j=0;break;case 5:ua(h);h.h=3;break;case 6:return h.return(g);case 3:e++;h.h=2;break;case 4:throw new X(\"Decryption failed for the given ciphertext.\");}})},uW=function(){};uW.prototype.Tj=function(a){if(!a)throw new X(\"Primitive set has to be non-null.\");return new sW(a)};\nuW.prototype.Oa=function(){return rW};function vW(a){var b=null;var c=a instanceof MU?F(a,JU,2):a;var d=F(c,FU,2);if(!d)throw new X(\"Params not set\");d=F(d,DU,1);if(!d)throw new X(\"KEM params not set\");d=GV(Sj(d,1));var e=vV(d),f=FV(kV(Aj(c,3)),e);c=FV(kV(Aj(c,4)),e);a instanceof MU&&(b=FV(kV(Aj(a,3)),e));a=b;b={kty:\"EC\",crv:sV(d),x:rV(f),y:rV(c),ext:!0};a&&(b.d=rV(a));return b};function wW(a){var b=F(a,DU,1);if(!b)throw new X(\"Invalid params - missing KEM params.\");var c=Sj(b,1);if(2!==c&&3!==c&&4!==c)throw new X(\"Invalid KEM params - unknown curve type.\");b=Sj(b,2);if(1!==b&&3!==b&&2!==b&&4!==b)throw new X(\"Invalid KEM params - unknown hash type.\");b=F(a,BU,2);if(!b)throw new X(\"Invalid params - missing DEM params.\");if(!F(b,zU,2))throw new X(\"Invalid DEM params - missing AEAD key template.\");b=Rj(F(b,zU,2),1);if(\"type.googleapis.com/google.crypto.tink.AesCtrHmacAeadKey\"!=\nb&&\"type.googleapis.com/google.crypto.tink.AesGcmKey\"!=b)throw new X(\"Invalid DEM params - \"+b+\" template is not supported by ECIES AEAD HKDF.\");a=Sj(a,3);if(1!==a&&2!==a&&3!==a)throw new X(\"Invalid key params - unknown EC point format.\");}function xW(a,b){XV(a.getVersion(),b);b=F(a,FU,2);if(!b)throw new X(\"Invalid public key - missing key params.\");wW(b);if(!lV(Aj(a,3))||!lV(Aj(a,4)))throw new X(\"Invalid public key - missing value of X or Y.\");};var yW=function(){};var zW=function(a){var b=Rj(a,1);switch(b){case \"type.googleapis.com/google.crypto.tink.AesCtrHmacAeadKey\":try{var c=uU(Aj(a,2))}catch(f){throw new X(\"Could not parse the given Uint8Array as a serialized proto of type.googleapis.com/google.crypto.tink.AesCtrHmacAeadKey.\");}if(!F(c,pU,1)||!F(c,rU,2))throw new X(\"Could not parse the given Uint8Array as a serialized proto of type.googleapis.com/google.crypto.tink.AesCtrHmacAeadKey.\");a=c;var d=F(a,pU,1);if(!d)throw new X(\"AES-CTR key format not set\");\nd=Qj(d,2);c=F(a,rU,2);if(!c)throw new X(\"HMAC key format not set\");c=d+Qj(c,2);break;case \"type.googleapis.com/google.crypto.tink.AesGcmKey\":try{var e=yU(Aj(a,2))}catch(f){throw new X(\"Could not parse the given Uint8Array as a serialized proto of type.googleapis.com/google.crypto.tink.AesGcmKey.\");}if(!Qj(e,2))throw new X(\"Could not parse the given Uint8Array as a serialized proto of type.googleapis.com/google.crypto.tink.AesGcmKey.\");a=e;c=Qj(a,2);break;default:throw new X(\"Key type URL \"+b+\" is not supported.\");\n}this.key=NV(b).Pd().Zd(a);this.g=b;this.te=c;this.hf=d};\nzW.prototype.jd=function(a){var b=this,c;return A(function(d){if(a.length!==b.te)throw new X(\"Key is not of the correct length, expected length: \"+b.te+\", but got key of length: \"+a.length+\".\");if(\"type.googleapis.com/google.crypto.tink.AesCtrHmacAeadKey\"===b.g){var e=b.key,f=F(e,hU,2);if(!f)throw new X(\"AES-CTR key not set\");Dj(f,3,a.slice(0,b.hf));f=F(e,lU,3);if(!f)throw new X(\"HMAC key not set\");Dj(f,3,a.slice(b.hf,b.te));c=e}else{if(!(b.key instanceof vU))throw new X(\"Key is not an AES-CTR key\");\nc=Dj(b.key,3,a)}return d.return(OV(TV,c,b.g))})};function AW(a,b,c,d,e){var f,g,h,k,m,n,p,r,t;return A(function(w){switch(w.h){case 1:if(!Number.isInteger(a))throw new Y(\"size must be an integer\");if(0>=a)throw new Y(\"size must be positive\");switch(b){case \"SHA-1\":f=20;if(5100<a)throw new Y(\"size too large\");break;case \"SHA-256\":f=32;if(8160<a)throw new Y(\"size too large\");break;case \"SHA-512\":f=64;if(16320<a)throw new Y(\"size too large\");break;default:throw new Y(b+\" is not supported\");}WV(c);WV(d);g=e;if(null==e||void 0===g||0==g.length)g=new Uint8Array(f);\nWV(g);return y(w,dW(b,g,f),2);case 2:return h=w.g,y(w,bW(h,c),3);case 3:return k=w.g,y(w,dW(b,k,f),4);case 4:h=w.g,m=1,n=0,p=new Uint8Array(0),r=new Uint8Array(a);case 5:return t=new Uint8Array(p.length+d.length+1),t.set(p,0),t.set(d,p.length),t[t.length-1]=m,y(w,bW(h,t),8);case 8:p=w.g;if(n+p.length<a)r.set(p,n),n+=p.length,m++;else{r.set(p.subarray(0,a-n),n);w.h=7;break}w.h=5;break;case 7:return w.return(r)}})};var BW=function(a){if(!a)throw new X(\"Recipient public key has to be non-null.\");if(\"public\"!==a.type||!a.algorithm)throw new X(\"Expected Crypto key of type: public.\");this.publicKey=a};\nBW.prototype.fh=function(a,b,c,d,e){var f=this,g,h,k,m,n,p,r,t,w,z;return A(function(I){switch(I.h){case 1:g=f.publicKey.algorithm;h=g.namedCurve;if(!h)throw new X(\"Curve has to be defined.\");return y(I,BV(h),2);case 2:return k=I.g,y(I,AV(k.privateKey,f.publicKey),3);case 3:return m=I.g,y(I,CV(k.publicKey),4);case 4:p=n=I.g;r=p.crv;if(!r)throw new X(\"Curve has to be defined.\");t=uV(r,b,n);w=mV(t,m);return y(I,AW(a,c,w,d,e),5);case 5:return z=I.g,I.return({key:z,token:t})}})};\nfunction CW(a){var b;return A(function(c){if(1==c.h)return y(c,DV(a),2);b=c.g;return c.return(new BW(b))})};var DW=function(a,b,c,d,e){if(!a)throw new X(\"KEM sender has to be non-null.\");if(!b)throw new X(\"HMAC algorithm has to be non-null.\");if(!c)throw new X(\"Point format has to be non-null.\");if(!d)throw new X(\"DEM helper has to be non-null.\");this.o=a;this.h=b;this.l=c;this.g=d;this.j=e};x(DW,yW);\nDW.prototype.encrypt=function(a,b){b=void 0===b?new Uint8Array(0):b;var c=this,d,e,f,g,h;return A(function(k){switch(k.h){case 1:return d=c.g.te,y(k,c.o.fh(d,c.l,c.h,b,c.j),2);case 2:return e=k.g,y(k,c.g.jd(e.key),3);case 3:return f=k.g,y(k,f.encrypt(a),4);case 4:return g=k.g,h=e.token,k.return(mV(h,g))}})};\nfunction EW(a,b,c,d,e){var f;return A(function(g){if(1==g.h){if(!a)throw new X(\"Recipient public key has to be non-null.\");if(!b)throw new X(\"HMAC algorithm has to be non-null.\");if(!c)throw new X(\"Point format has to be non-null.\");if(!d)throw new X(\"DEM helper has to be non-null.\");return y(g,CW(a),2)}f=g.g;return g.return(new DW(f,b,c,d,e))})};var FW=function(){};FW.prototype.Zd=function(){throw new X(\"This operation is not supported for public keys. Use EciesAeadHkdfPrivateKeyManager to generate new keys.\");};var GW=function(){this.g=new FW};l=GW.prototype;\nl.xb=function(a,b){var c=this,d,e,f,g,h,k,m,n,p,r;return A(function(t){if(a!==c.Oa())throw new X(\"Requested primitive type which is not supported by this key manager.\");if(b instanceof YU){if(\"type.googleapis.com/google.crypto.tink.EciesAeadHkdfPublicKey\"!==Rj(b,1))throw new X(\"Key type \"+Rj(b,1)+\" is not supported. This key manager supports type.googleapis.com/google.crypto.tink.EciesAeadHkdfPublicKey.\");try{var w=LU(Aj(b,2))}catch(z){throw new X(\"Input cannot be parsed as type.googleapis.com/google.crypto.tink.EciesAeadHkdfPublicKey key-proto.\");\n}if(!F(w,FU,2)||!Aj(w,3)||!Aj(w,4))throw new X(\"Input cannot be parsed as type.googleapis.com/google.crypto.tink.EciesAeadHkdfPublicKey key-proto.\");}else if(b instanceof JU)w=b;else throw new X(\"Key type is not supported. This key manager supports type.googleapis.com/google.crypto.tink.EciesAeadHkdfPublicKey.\");d=w;xW(d,c.getVersion());e=vW(d);f=F(d,FU,2);g=F(f,BU,2);if(!g)throw new X(\"DEM params not set\");h=F(g,zU,2);k=new zW(h);m=IV(Sj(f,3));n=F(f,DU,1);if(!n)throw new X(\"KEM params not set\");\np=HV(Sj(n,2));r=kV(Aj(n,11));return t.return(EW(e,p,m,k,r))})};l.Nd=function(a){return a===this.Ua()};l.Ua=function(){return\"type.googleapis.com/google.crypto.tink.EciesAeadHkdfPublicKey\"};l.Oa=function(){return yW};l.getVersion=function(){return 0};l.Pd=function(){return this.g};var HW=function(a){if(!a)throw new X(\"Private key has to be non-null.\");if(\"private\"!==a.type||!a.algorithm)throw new X(\"Expected crypto key of type: private.\");this.g=a};HW.prototype.Yg=function(a,b,c,d,e,f){var g=this,h,k,m,n,p,r,t;return A(function(w){switch(w.h){case 1:h=g.g.algorithm;k=h.namedCurve;if(!k)throw new X(\"Curve has to be defined.\");m=zV(k,c,a);return y(w,DV(m),2);case 2:return n=w.g,y(w,AV(g.g,n),3);case 3:return p=w.g,r=mV(a,p),y(w,AW(b,d,r,e,f),4);case 4:return t=w.g,w.return(t)}})};\nfunction PW(a){var b;return A(function(c){if(1==c.h)return y(c,EV(a),2);b=c.g;return c.return(new HW(b))})};var aX=function(a,b,c,d,e,f){if(!a)throw new X(\"Recipient private key has to be non-null.\");if(!b)throw new X(\"KEM recipient has to be non-null.\");if(!c)throw new X(\"HKDF hash algorithm has to be non-null.\");if(!d)throw new X(\"Point format has to be non-null.\");if(!e)throw new X(\"DEM helper has to be non-null.\");a=a.crv;if(!a)throw new X(\"Curve has to be defined.\");a=tV(a);a:{switch(d){case 1:a=2*vV(a)+1;break a;case 2:a=vV(a)+1;break a;case 3:a=2*vV(a);break a}a=void 0}this.A=b;this.j=c;this.o=d;\nthis.h=e;this.g=a;this.l=f};x(aX,rW);aX.prototype.decrypt=function(a,b){var c=this,d,e,f;return A(function(g){if(1==g.h){if(a.length<c.g)throw new X(\"Ciphertext is too short.\");d=a.slice(0,c.g);e=a.slice(c.g,a.length);return y(g,c.jd(d,b),2)}f=g.g;return g.return(f.decrypt(e))})};aX.prototype.jd=function(a,b){var c=this,d;return A(function(e){if(1==e.h)return b||(b=new Uint8Array(0)),y(e,c.A.Yg(a,c.h.te,c.o,c.j,b,c.l),2);d=e.g;return e.return(c.h.jd(d))})};\nfunction bX(a,b,c,d,e){var f;return A(function(g){if(1==g.h){if(!a)throw new X(\"Recipient private key has to be non-null.\");if(!b)throw new X(\"HKDF hash algorithm has to be non-null.\");if(!c)throw new X(\"Point format has to be non-null.\");if(!d)throw new X(\"DEM helper has to be non-null.\");if(!a)throw new X(\"Recipient private key has to be non-null.\");return y(g,PW(a),2)}f=g.g;return g.return(new aX(a,f,b,c,d,e))})};var cX=function(){};\ncX.prototype.Zd=function(a){var b,c,d,e,f,g,h,k,m;return A(function(n){switch(n.h){case 1:if(!a)throw new X(\"Key format has to be non-null.\");if(a instanceof Uint8Array){try{var p=IU(a)}catch(z){throw new X(\"Input cannot be parsed as type.googleapis.com/google.crypto.tink.EciesAeadHkdfPrivateKey key format proto.\");}if(!F(p,FU,1))throw new X(\"Input cannot be parsed as type.googleapis.com/google.crypto.tink.EciesAeadHkdfPrivateKey key format proto.\");}else if(a instanceof HU)p=a;else throw new X(\"Expected type.googleapis.com/google.crypto.tink.EciesAeadHkdfPrivateKey key format proto.\");\nb=p;p=F(b,FU,1);if(!p)throw new X(\"Invalid key format - missing key params.\");wW(p);c=F(b,FU,1);if(!c)throw new X(\"Params not set\");d=F(c,DU,1);if(!d)throw new X(\"KEM params not set\");e=Sj(d,1);f=GV(e);g=sV(f);return y(n,BV(g),2);case 2:return h=n.g,y(n,CV(h.publicKey),3);case 3:return k=n.g,y(n,CV(h.privateKey),4);case 4:m=n.g;p=n.return;var r=k.x;var t=k.y;if(void 0===r)throw new X(\"x must be set\");if(void 0===t)throw new X(\"y must be set\");var w=new JU;w=Cj(w,1,0,0);w=Ij(w,2,c);r=pV(r);r=Dj(w,\n3,r);t=pV(t);r=Dj(r,4,t);t=m.d;if(void 0===t)throw new X(\"d must be set\");w=new MU;w=Cj(w,1,0,0);r=Ij(w,2,r);t=pV(t);t=Dj(r,3,t);return p.call(n,t)}})};var dX=function(){this.g=new cX};l=dX.prototype;\nl.xb=function(a,b){var c=this,d,e,f,g,h,k,m,n,p,r,t;return A(function(w){if(a!==c.Oa())throw new X(\"Requested primitive type which is not supported by this key manager.\");if(b instanceof YU){if(\"type.googleapis.com/google.crypto.tink.EciesAeadHkdfPrivateKey\"!==Rj(b,1))throw new X(\"Key type \"+Rj(b,1)+\" is not supported. This key manager supports type.googleapis.com/google.crypto.tink.EciesAeadHkdfPrivateKey.\");var z=Aj(b,2);try{var I=NU(z)}catch(v){throw new X(\"Input cannot be parsed as type.googleapis.com/google.crypto.tink.EciesAeadHkdfPrivateKey key-proto.\");\n}if(!F(I,JU,2)||!Aj(I,3))throw new X(\"Input cannot be parsed as type.googleapis.com/google.crypto.tink.EciesAeadHkdfPrivateKey key-proto.\");z=I}else if(b instanceof MU)z=b;else throw new X(\"Key type is not supported. This key manager supports type.googleapis.com/google.crypto.tink.EciesAeadHkdfPrivateKey.\");d=z;XV(d.getVersion(),0);if(!Aj(d,3))throw new X(\"Invalid private key - missing private key value.\");z=F(d,JU,2);if(!z)throw new X(\"Invalid private key - missing public key information.\");xW(z,\n0);e=vW(d);f=F(d,JU,2);if(!f)throw new X(\"Public key not set\");g=F(f,FU,2);if(!g)throw new X(\"Params not set\");h=F(g,BU,2);if(!h)throw new X(\"DEM params not set\");k=F(h,zU,2);if(!k)throw new X(\"Key template not set\");m=new zW(k);n=IV(Sj(g,3));p=F(g,DU,1);if(!p)throw new X(\"KEM params not set\");r=HV(Sj(p,2));t=kV(Aj(p,11));return w.return(bX(e,r,n,m,t))})};l.Nd=function(a){return a===this.Ua()};l.Ua=function(){return\"type.googleapis.com/google.crypto.tink.EciesAeadHkdfPrivateKey\"};l.Oa=function(){return rW};\nl.getVersion=function(){return 0};l.Pd=function(){return this.g};var eX=function(a){this.g=a};x(eX,yW);eX.prototype.encrypt=function(a,b){var c=this,d,e,f,g;return A(function(h){if(1==h.h){if(!a)throw new X(\"Plaintext has to be non-null.\");d=c.g.h;if(!d)throw new X(\"Primary not set.\");e=d.xb();return y(h,e.encrypt(a,b),2)}f=h.g;g=d.identifier;return h.return(mV(g,f))})};var fX=function(){};fX.prototype.Tj=function(a){if(!a)throw new X(\"Primitive set has to be non-null.\");if(!a.h)throw new X(\"Primary has to be non-null.\");return new eX(a)};fX.prototype.Oa=function(){return yW};var hX=gX(1,0),iX=gX(2,16),jX=gX(2,18),kX=gX(2,1),lX=gX(2,3),mX=gX(2,1),nX=gX(2,2),oX=qV(\"KEM\"),pX=qV(\"HPKE\"),qX=qV(\"HPKE-v1\");function gX(a,b){for(var c=new Uint8Array(a),d=0;d<a;d++)c[d]=b>>8*(a-d-1)&255;return c}function rX(a){var b=a.Hc;return mV(qX,a.ib,qV(a.Ic),b)}function sX(a){var b=a.pd,c=a.info,d=a.ib;return mV(gX(2,a.length),qX,d,qV(b),c)}function tX(a){switch(a){case 2:return 1;case 4:return 3;default:throw new Y(\"Unrecognized NIST HPKE KEM identifier\");}}\nfunction uX(a,b){var c;return A(function(d){return 1==d.h?(c=zV(a,1,b),y(d,DV(c),2)):d.return(d.g)})}function vX(a){var b=a.Xg,c=a.publicKey,d=a.privateKey,e;return A(function(f){return 1==f.h?(e=zV(b,1,c),e.d=rV(d),y(f,EV(e),2)):f.return(f.g)})}function wX(a){var b,c;return A(function(d){if(1==d.h)return b=a.algorithm,y(d,CV(a),2);c=d.g;if(!c.crv)throw new X(\"Curve has to be defined.\");return d.return(uV(b.namedCurve,1,c))})};var xX=function(a,b,c,d){this.gh=a;this.key=b;this.j=c;this.h=d;this.g=BigInt(0);this.l=(BigInt(1)<<BigInt(96))-BigInt(1)};xX.prototype.seal=function(a,b){var c=this,d;return A(function(e){return 1==e.h?(d=yX(c),y(e,c.h.seal({key:c.key,nonce:d,Ul:a,Jg:b}),2)):e.return(e.g)})};xX.prototype.open=function(a,b){var c=this,d;return A(function(e){d=yX(c);return e.return(c.h.open({key:c.key,nonce:d,Tk:a,Jg:b}))})};\nvar yX=function(a){for(var b=a.g,c=new Uint8Array(12),d=0;12>d;d++)c[d]=Number(b>>BigInt(8*(12-d-1)))&255;b=a.j;if(b.length!==c.length)throw new Y(\"Both byte arrays should be of the same length\");d=new Uint8Array(b.length);for(var e=0;e<d.length;e++)d[e]=b[e]^c[e];if(a.g>=a.l)throw new X(\"message limit reached\");a.g+=BigInt(1);return d};\nfunction zX(a,b,c,d,e,f){var g,h,k,m,n,p,r;return A(function(t){switch(t.h){case 1:a:{switch(e.Kf){case 16:var w=mX;break a;case 32:w=nX;break a}w=void 0}a:{switch(d.Hf){case \"SHA-256\":var z=kX;break a;case \"SHA-512\":z=lX;break a}z=void 0}g=mV(pX,AX(c),z,w);return y(t,BX(d,{Hc:new Uint8Array(0),Ic:\"psk_id_hash\",ib:g}),2);case 2:return h=t.g,y(t,BX(d,{Hc:f,Ic:\"info_hash\",ib:g}),3);case 3:return k=t.g,m=mV(hX,h,k),y(t,BX(d,{Hc:new Uint8Array(0),Ic:\"secret\",ib:g,salt:b}),4);case 4:return n=t.g,y(t,CX(d,\n{tj:n,info:m,pd:\"key\",ib:g,length:e.Kf}),5);case 5:return p=t.g,y(t,CX(d,{tj:n,info:m,pd:\"base_nonce\",ib:g,length:12}),6);case 6:return r=t.g,t.return(new xX(a,p,r,e))}})}function DX(a,b,c,d,e){var f,g,h;return A(function(k){return 1==k.h?y(k,b.fh(a),2):3!=k.h?(f=k.g,g=f.gh,h=f.hm,y(k,zX(g,h,b,c,d,e),3)):k.return(k.g)})}function EX(a,b,c,d,e,f){var g;return A(function(h){return 1==h.h?y(h,c.Yg(a,b),2):3!=h.h?(g=h.g,y(h,zX(a,g,c,d,e,f),3)):h.return(h.g)})};var FX=function(a,b){this.privateKey=a;this.publicKey=b},GX=function(a){return A(function(b){return 1==b.h?y(b,wX(a.publicKey),2):b.return(b.g)})};function HX(a){var b=a.privateKey,c=a.publicKey,d=a.Xg,e,f;return A(function(g){if(1==g.h){if(!b)throw new Y(\"KEM private key was null or undefined\");if(!c)throw new Y(\"KEM public key was null or undefined\");return y(g,uX(sV(d),c),2)}if(3!=g.h)return e=g.g,y(g,vX({Xg:sV(d),publicKey:c,privateKey:b}),3);f=g.g;return g.return(new FX(f,e))})}\nfunction IX(a){return A(function(b){JX(a.privateKey,\"private\");JX(a.publicKey,\"public\");return b.return(new FX(a.privateKey,a.publicKey))})}function JX(a,b){if(b!==a.type)throw new Y(\"keyPair \"+b+\" key was of type \"+a.type);a=a.algorithm;if(\"ECDH\"!==a.name)throw new Y(\"keyPair \"+b+\" key should be ECDH but found \"+a.name);};var KX=function(a){this.Kf=a};KX.prototype.seal=function(a){var b=a.key,c=a.nonce,d=a.Ul,e=a.Jg,f=this,g;return A(function(h){if(1==h.h){if(b.length!==f.Kf)throw new X(\"Unexpected key length: \"+b.length.toString());return y(h,mW({key:b,vc:!1}),2)}return 3!=h.h?(g=h.g,y(h,g.encrypt(c,d,e),3)):h.return(h.g)})};\nKX.prototype.open=function(a){var b=a.key,c=a.nonce,d=a.Tk,e=a.Jg,f=this,g;return A(function(h){if(1==h.h){if(b.length!==f.Kf)throw new X(\"Unexpected key length: \"+b.length.toString());return y(h,mW({key:b,vc:!1}),2)}g=h.g;return h.return(g.decrypt(c,d,e))})};var LX=function(a){this.Hf=a},BX=function(a,b){var c=b.Hc,d=b.Ic,e=b.ib,f=b.salt;return A(function(g){return 1==g.h?y(g,MX(a,rX({Ic:d,Hc:c,ib:e}),f),2):g.return(g.g)})},CX=function(a,b){var c=b.tj,d=b.info,e=b.pd,f=b.ib,g=b.length;return A(function(h){return 1==h.h?y(h,a.expand(c,sX({pd:e,info:d,ib:f,length:g}),g),2):h.return(h.g)})},NX=function(a,b){var c=b.Hc,d=b.Ic,e=b.info,f=b.pd,g=b.ib,h=b.length,k=b.salt,m;return A(function(n){return 1==n.h?y(n,MX(a,rX({Ic:d,Hc:c,ib:g}),k),2):3!=n.h?(m=n.g,\ny(n,a.expand(m,sX({pd:f,info:e,ib:g,length:h}),h),3)):n.return(n.g)})};\nLX.prototype.expand=function(a,b,c){var d=this,e,f,g,h,k,m,n;return A(function(p){switch(p.h){case 1:if(!Number.isInteger(c))throw new X(\"length must be an integer\");if(0>=c)throw new X(\"length must be positive\");e=OX(d);if(c>255*e)throw new X(\"length too large\");WV(b);return y(p,dW(d.Hf,a,e),2);case 2:f=p.g,g=1,h=0,k=new Uint8Array(0),m=new Uint8Array(c);case 3:return n=new Uint8Array(k.length+b.length+1),n.set(k,0),n.set(b,k.length),n[n.length-1]=g,y(p,bW(f,n),6);case 6:k=p.g;if(h+k.length<c)m.set(k,\nh),h+=k.length,g++;else{m.set(k.subarray(0,c-h),h);p.h=5;break}p.h=3;break;case 5:return p.return(m)}})};var MX=function(a,b,c){var d,e,f,g;return A(function(h){if(1==h.h)return WV(b),d=OX(a),(null==(e=c)?0:e.length)||(c=new Uint8Array(d)),WV(c),y(h,dW(a.Hf,c,d),2);if(3!=h.h)return f=h.g,y(h,bW(f,b),3);g=h.g;return h.return(g)})},OX=function(a){switch(a.Hf){case \"SHA-256\":return 32;case \"SHA-512\":return 64}};var PX=function(a,b){this.j=a;this.g=b},QX=function(a){switch(a){case 1:return new PX(new LX(\"SHA-256\"),1);case 3:return new PX(new LX(\"SHA-512\"),3)}};PX.prototype.h=function(a,b,c){var d=this,e,f;return A(function(g){return 1==g.h?(e=mV(b,c),f=mV(oX,AX(d)),y(g,NX(d.j,{Hc:a,Ic:\"eae_prk\",info:e,pd:\"shared_secret\",ib:f,length:OX(d.j)}),2)):g.return(g.g)})};\nPX.prototype.l=function(a,b){var c=this,d,e,f,g,h;return A(function(k){switch(k.h){case 1:return y(k,uX(sV(c.g),a),2);case 2:return d=k.g,y(k,AV(b.privateKey,d),3);case 3:return e=k.g,y(k,GX(b),4);case 4:return f=k.g,y(k,c.h(e,f,a),5);case 5:return g=k.g,h={hm:g,gh:f},k.return(h)}})};PX.prototype.fh=function(a){var b=this,c,d,e,f;return A(function(g){switch(g.h){case 1:return y(g,BV(sV(b.g)),2);case 2:return c=g.g,d=b,e=d.l,f=a,y(g,IX(c),4);case 4:return y(g,e.call(d,f,g.g),3);case 3:return g.return(g.g)}})};\nPX.prototype.Yg=function(a,b){var c=this,d,e,f,g,h,k;return A(function(m){switch(m.h){case 1:return d=b.privateKey,y(m,uX(sV(c.g),a),2);case 2:return e=m.g,y(m,AV(d,e),3);case 3:return f=m.g,g=c,h=g.h,k=a,y(m,GX(b),4);case 4:return m.return(h.call(g,f,k,m.g))}})};var AX=function(a){switch(a.g){case 1:return iX;case 3:return jX}};/*\n\n Copyright 2023 Google LLC\n SPDX-License-Identifier: Apache-2.0\n*/\nvar RX=function(a){switch(Sj(a,1)){case 2:return QX(1);case 4:return QX(3);default:throw new Y(\"Unrecognized HPKE KEM identifier\");}},SX=function(a){switch(Sj(a,2)){case 1:return new LX(\"SHA-256\");case 3:return new LX(\"SHA-512\");default:throw new Y(\"Unrecognized HPKE KDF identifier\");}},TX=function(a){switch(a.jd()){case 1:return new KX(16);case 2:return new KX(32);default:throw new Y(\"Unrecognized HPKE AEAD identifier\");}};var UX=function(a,b,c,d,e){if(!a)throw new Y(\"Recipient private key must be non-null.\");if(!b)throw new Y(\"KEM algorithm must be 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n=YP(k)||XP(k)||PP(k)||QP(k);if(YP(k)){$0(\"action\");var p=new J_(k,e,h,m,n);n=new hZ(p,h,e.g,m,n)}else if(null!=vP(k)&&0!==VL.g)$0(\"vpaid\"),n=new k1(k,e,h);else if(ZP(k))$0(\"simid\"),n=new a0(k,e,h,m),n=new u0({Gk:n,im:e,ad:k});else if(OP(k,\"linear\"))$0(\"video\"),n=new J_(k,e,h,m,n);else if(v1(k))$0(\"nonlinear\"),n=new VZ(k,e,h);else{h=null;break b}null!=KP(k)&&(k=new d_(n,e,new x1,h),$0(\"multiple_fb\"),n=\nnew d0(k,e.g,h));h=n}null!=h&&f.push(h)}a=f}if(0==a.length)throw Error(\"Manager creation failure, failed to determine ad type.\");$0(\"multiple_pod\");return new d0(new OZ(a),d,c,b.h)};var y1=function(a,b,c,d){this.j=a;this.h=b;this.g=c;this.l=d};y1.prototype.build=function(a,b){a.enablePreloading&&rN()?uZ(this.g.h,2):uZ(this.g.h,1);if(this.h instanceof WN){var c=this.h,d=this.j,e=this.g,f=new x1;gN().report(100,{type:\"vmap\"});a=new U0(f,c,d,b,a,e)}else b=this.h,c=this.g,d=new x1,w1(b),a=d.create(b,c,a);this.l(a);return a};var z1=function(a,b,c,d,e){mn.call(this);var 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\ No newline at end of file