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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

    Bahasa Indonesia; Italiano; ... Butyne is an alkyne that contains 4 carbon and 6 hydrogen. It contains one triple bond and has two isomeric organic chemical compounds:

  4. 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 strained ...

  5. Category:Alkynes - Wikipedia

    en.wikipedia.org/wiki/Category:Alkynes

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  6. 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 ...

  7. Diacetylene - Wikipedia

    en.wikipedia.org/wiki/Diacetylene

    Bahasa Indonesia; Italiano; ... This compound may be made by the dehydrohalogenation of 1,4-dichloro-2-butyne by potassium hydroxide (in alcoholic medium) at ~70°C: [1]

  8. Category:Alkyne derivatives - Wikipedia

    en.wikipedia.org/wiki/Category:Alkyne_derivatives

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  9. 1-Butyne - Wikipedia

    en.wikipedia.org/wiki/1-Butyne

    1-Butyne is an organic compound with the formula CH 3 CH 2 C≡CH. It is a terminal alkyne. The compound is a common terminal alkyne substrate in diverse studies of catalysis. It is a colorless combustible gas. [1] 1-Butyne participates in reactions typical for terminal alkynes, such as alkyne metathesis, [2] hydrogenation, condensation with ...