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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. Benzylacetone - Wikipedia

    en.wikipedia.org/wiki/Benzylacetone

    Benzylacetone (IUPAC name: 4-phenylbutan-2-one) is a liquid with a sweet, flowery smell that is considered to be the most abundant attractant compound in flowers (e.g. Coyote Tobacco, Nicotiana attenuata) [1] [2] and one of volatile components of cocoa.

  4. Butyrophenone - Wikipedia

    en.wikipedia.org/wiki/Butyrophenone

    Butyrophenone is an organic compound with the formula C 6 H 5 C(O)C 3 H 7.It is a colorless liquid. The butyrophenone structure—a ketone flanked by a phenyl ring and a butyl chain—forms the basis for many other chemicals containing various substituents.

  5. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    C 2 H 4 + 1/ 2 O 2 → C 2 H 4 O. Alkenes react with ozone, leading to the scission of the double bond. The process is called ozonolysis. Often the reaction procedure includes a mild reductant, such as dimethylsulfide (SMe 2): RCH=CHR' + O 3 + SMe 2 → RCHO + R'CHO + O=SMe 2 R 2 C=CHR' + O 3 → R 2 CHO + R'CHO + O=SMe 2

  6. Benzylideneacetone - Wikipedia

    en.wikipedia.org/wiki/Benzylideneacetone

    As with most methyl ketones, benzylideneacetone is moderately acidic at the alpha position, and it can be readily deprotonated to form the corresponding enolate [6]. The compound undergoes the reactions expected for its collection of functional groups: e.g., the double bond adds bromine, the heterodiene adds electron-rich alkenes in Diels-Alder reactions to give dihydropyrans, the methyl group ...

  7. Butene - Wikipedia

    en.wikipedia.org/wiki/Butene

    Butene, also known as butylene, is an alkene with the formula C 4 H 8. The word butene may refer to any of the individual compounds. They are colourless gases that ...

  8. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    Enolization is an example of isomerization, as is tautomerization. [2] When the isomerization occurs intramolecularly it may be called a rearrangement reaction. [citation needed] When the activation energy for the isomerization reaction is sufficiently small, both isomers will exist in a temperature-dependent equilibrium with each other.

  9. Methyl vinyl ketone - Wikipedia

    en.wikipedia.org/wiki/Methyl_vinyl_ketone

    Methyl vinyl ketone (MVK, IUPAC name: butenone) is the organic compound with the formula CH 3 C(O)CH=CH 2. It is a reactive compound classified as an enone , in fact the simplest example thereof. It is a colorless, flammable, highly toxic liquid with a pungent odor.