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  2. Dimethylbutadiene - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutadiene

    Dimethylbutadiene, formally referred to as 2,3-dimethyl-1,3-butadiene, is an organic compound with the formula (CH 3) 2 C 4 H 4. It is colorless liquid which served an important role in the early history of synthetic rubber .

  3. Dimethylbutene - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutene

    This article about a hydrocarbon is a stub. You can help Wikipedia by expanding it.

  4. 2,3-Dimethylbutane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylbutane

    This article about a hydrocarbon is a stub. You can help Wikipedia by expanding it.

  5. 1,2-Butadiene - Wikipedia

    en.wikipedia.org/wiki/1,2-Butadiene

    This page was last edited on 30 October 2024, at 13:41 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  6. Category:Alkadienes - Wikipedia

    en.wikipedia.org/wiki/Category:Alkadienes

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  7. Diels–Alder reaction - Wikipedia

    en.wikipedia.org/wiki/Diels–Alder_reaction

    In 1910, Sergey Lebedev systematically investigated thermal polymerization of three conjugated dienes (butadiene, isoprene and dimethylbutadiene), a process now recognized as a Diels-Alder self-reaction, providing a detailed analysis of the dimerization products and recognizing the importance of the conjugated system in the process. [69]

  8. 2,2-Dimethylbutane - Wikipedia

    en.wikipedia.org/wiki/2,2-Dimethylbutane

    Butlerov's student V. Goryainov originally discovered neohexane in 1872 by cross-coupling of zinc ethyl with tert-butyl iodide. [5]2,2-Dimethylbutane can be synthesised by the hydroisomerisation of 2,3-dimethylbutane using an acid catalyst.

  9. Talk:Dimethylbutadiene - Wikipedia

    en.wikipedia.org/wiki/Talk:Dimethylbutadiene

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