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  2. 2-Butyne - Wikipedia

    en.wikipedia.org/wiki/2-butyne

    2-Butyne (dimethylacetylene, crotonylene or but-2-yne) is an alkyne with chemical formula CH 3 C≡CCH 3. Produced artificially, it is a colorless, volatile, pungent liquid at standard temperature and pressure .

  3. Butyne - Wikipedia

    en.wikipedia.org/wiki/Butyne

    Butyne is an alkyne that contains 4 carbon and 6 hydrogen. It contains one triple bond and has two isomeric organic chemical compounds: 1-Butyne (ethylacetylene)

  4. Cyclopropene - Wikipedia

    en.wikipedia.org/wiki/Cyclopropene

    The synthesis of purely aliphatic cyclopropenes was first illustrated by the copper-catalyzed additions of carbenes to alkynes. In the presence of a copper catalyst, ethyl diazoacetate reacts with acetylenes to give cyclopropenes. 1,2-Dimethylcyclopropene-3-carboxylate arises via this method from 2-butyne. Copper, as copper sulfate and copper ...

  5. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    The C≡C bond distance of 118 picometers (for C 2 H 2) is much shorter than the C=C distance in alkenes (132 pm, for C 2 H 4) or the C–C bond in alkanes (153 pm). [3] Illustrative alkynes: a, acetylene, b, two depictions of propyne, c, 1-butyne, d, 2-butyne, e, the naturally occurring 1-phenylhepta-1,3,5-triyne, and f, the

  6. 2-Methyl-2-butene - Wikipedia

    en.wikipedia.org/wiki/2-Methyl-2-butene

    2-Methyl-2-butene, 2m2b, 2-methylbut-2-ene, beta-isoamylene, or Trimmethylethylene is an alkene hydrocarbon with the molecular formula C 5 H 10. Used as a free radical scavenger in trichloromethane (chloroform) and dichloromethane (methylene chloride). It is also used to scavenge hypochlorous acid (HOCl) in the Pinnick oxidation.

  7. 2-Methylbut-3-yn-2-ol - Wikipedia

    en.wikipedia.org/wiki/2-Methylbut-3-yn-2-ol

    [2] 2-Methylbut-3-yn-2-ol is produced on an industrial scale as a precursor to terpenes and terpenoids. 2-Methylbut-3-yn-2-ol is an intermediate in this industrial route to geraniol. [3] 2-Methylbut-3-yn-2-ol also is used as a monoprotected version of acetylene. For example, after arylation at carbon, the acetone can be removed with base: [4]

  8. Propyne - Wikipedia

    en.wikipedia.org/wiki/Propyne

    This nucleophilic reagent adds to carbonyl groups, producing alcohols and esters. [7] Whereas purified propyne is expensive, MAPP gas could be used to cheaply generate large amounts of the reagent. [8] Propyne, along with 2-butyne, is also used to synthesize alkylated hydroquinones in the total synthesis of vitamin E. [9]

  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.

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