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  2. But-2-ene - Wikipedia

    en.wikipedia.org/wiki/But-2-ene

    But-2-ene is an acyclic alkene with four carbon atoms. It is the simplest alkene exhibiting cis/trans-isomerism (also known as (E/Z)-isomerism); that is, it exists as two geometric isomers cis-but-2-ene ((Z)-but-2-ene) and trans-but-2-ene ((E)-but-2-ene). It is a petrochemical, produced by the catalytic cracking of crude oil or the dimerization ...

  3. Butene - Wikipedia

    en.wikipedia.org/wiki/Butene

    Skeletal formula 3D model 1-butene, ... cis-2-butene, cis-β ... In the chemical structures above, the small blue numbers in the structure images are the numbering of ...

  4. File:Cis-2-butene.svg - Wikipedia

    en.wikipedia.org/wiki/File:Cis-2-butene.svg

    English: Skeletal diagram of cis-2-butene. Date: 10 August 2008: Source: ... Structure des molécules/La stéréoisométrie ZE; Usage on fr.wiktionary.org cis;

  5. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    Very often, cis–trans stereoisomers contain double bonds or ring structures. In both cases the rotation of bonds is restricted or prevented. [4] When the substituent groups are oriented in the same direction, the diastereomer is referred to as cis, whereas when the substituents are oriented in opposing directions, the diastereomer is referred to as trans.

  6. File:Cis-2-Buten.svg - Wikipedia

    en.wikipedia.org/wiki/File:Cis-2-Buten.svg

    English: Structure of cis-2-butene. Date: 24 March 2007: Source: Own work: Author: NEUROtiker: Permission (Reusing this file) Own work, all rights released (Public ...

  7. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    [5] [6] Examples of the latter are the enantiomers, whose molecules are mirror images of each other, and the cis and trans versions of 2-butene. Among the structural isomers, one can distinguish several classes including skeletal isomers, positional isomers (or regioisomers), functional isomers, tautomers, [7] and structural isotopomers. [8]

  8. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    Trans-alkenes are about 1 kcal/mol more stable than cis-alkenes. An example of this effect is cis- vs trans-2-butene. The difference is attributed to unfavorable non-bonded interactions in the cis isomer. This effects helps to explain the formation of trans-fats in food processing. In some cases, the isomerization can be reversed using UV-light.

  9. Isobutylene - Wikipedia

    en.wikipedia.org/wiki/Isobutylene

    Isobutylene (or 2-methylpropene) is a hydrocarbon with the chemical formula (CH 3) 2 C=CH 2. It is a four-carbon branched alkene (olefin), one of the four isomers of butylene . It is a colorless flammable gas, and is of considerable industrial value.