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alkene
(redirected from Carbon-carbon double bond)

   Also found in: Dictionary/thesaurus, Medical, Wikipedia 0.01 sec.
alkene (ăl`kēn), any of a group of aliphatic hydrocarbons whose molecules contain one or more carbon-carbon double bonds (see chemical bond chemical bond, mechanism whereby atoms combine to form molecules. There is a chemical bond between two atoms or groups of atoms when the forces acting between them are strong enough to lead to the formation of an aggregate with sufficient stability to be regarded as
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). Alkenes with only one double bond have the general formula CnH2n. In the International Union of Pure and Applied Chemistry (IUPAC) system of chemical nomenclature, the name of an alkene is derived from the name of the corresponding alkane alkane , any of a group of aliphatic hydrocarbons whose molecules contain only single bonds (see chemical bond). Alkanes have the general chemical formula CnH2n+2.
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 by replacing the -ane alkane suffix with -ene and, if necessary, adding a prefix to indicate the location of the double bond in the molecule. The IUPAC name of the simplest alkene, H2C=CH2, is ethene, which is derived from ethane. Propene is related to propane. Two alkenes, 1-butene and 2-butene, are related to butane; these two compounds, which differ in the location of the double bond in their molecules, are structural isomers isomer , in chemistry, one of two or more compounds having the same molecular formula but different structures (arrangements of atoms in the molecule). Isomerism is the occurrence of such compounds. Isomerism was first recognized by J. J. Berzelius in 1827.
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. In addition to these IUPAC names, many of the alkenes have common names, e.g., ethene is called ethylene and propene propylene. The alkenes as a group are sometimes called the ethylene series. Since the carbon-carbon double bond is sometimes called an olefinic linkage, the alkenes are sometimes called the olefins. Many of the reactions in which alkenes take part involve the cleavage of half the carbon-carbon double bond and subsequent formation of two single bonds, one to each of the adjacent carbon atoms. Such reactions include hydrogenation, with the formation of an alkane, and hydration, with the formation of an alcohol.

olefin

 or alkene

Any unsaturated hydrocarbon containing one or more pairs of carbon atoms linked by a double bond (see covalent bond, saturation). Olefins may be classified by whether the double bond is in a ring (cyclic) or a chain (acyclic, or aliphatic) or by the number of double bonds (monoolefin, diolefin, etc.). Rare in nature, olefins are obtained by the cracking of petroleum fractions at high temperatures. The simplest ones (ethylene, propylene, butylene, butadiene, and isoprene) are the basis of the petrochemicals industry. They react by adding other chemical agents at the double bond to form derivatives or polymers.


alkene
a. any unsaturated aliphatic hydrocarbon with the general formula CnH2n
b. (as modifier): alkene series

alkene [′al‚kēn]
(organic chemistry)
One of a class of unsaturated aliphatic hydrocarbons containing one or more carbon-to-carbon double bonds.


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Highly versatile molecules that contain carbon-carbon double bonds, alkenes, or olefins, are ubiquitous in medicinally relevant and biologically active molecules.
4, wherein the epoxidized compound is an epoxidation product of fatty acid moieties having one or more carbon-carbon double bonds, wherein less than 20% mole of the fatty acid moieties contain three or more carbon-carbon double bonds, and wherein greater than 60% mole of the fatty acid moieties contain two carbon-carbon double bonds; and combining the pigment and the fatty (meth)acrylate in a liquid carrier medium.
By targeting the carbon-carbon double bond, which is usually difficult to break, metathesis reactions provide "a new way to link molecules together," says Ronald Breslow, a chemist at Columbia University and Grubbs' Ph.
 
 
 
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