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  2. 4-Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/4-Methylcyclohexene

    4-Methylcyclohexene is an organic compound consisting of cyclohexene with a methyl group substituent attached to carbon most distant from the alkene group. Two other structural isomers are known: 1-methylcyclohexene and 3-methylcyclohexene .

  3. Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexene

    Methylcyclohexene can refer to any of three compounds: 1-Methylcyclohexene; 3-Methylcyclohexene; 4-Methylcyclohexene This page was last edited on 18 November ...

  4. Work-up - Wikipedia

    en.wikipedia.org/wiki/Work-up

    Synthesis of 4-methylcyclohexene with work-up step in red. A concentrated solution of sodium chloride in water, known as a brine solution, is added to the mixture and the layers are allowed to separate. The brine is used to remove any acid or water from the organic layer.

  5. Methylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexane

    Most methylcyclohexane is extracted from petroleum but it can be also produced by catalytic hydrogenation of toluene: CH 3 C 6 H 5 + 3 H 2 → CH 3 C 6 H 11. The hydrocarbon is a minor component of automobile fuel, with its share in US gasoline varying between 0.3 and 1.7% in early 1990s [10] and 0.1 to 1% in 2011. [11]

  6. Evelyn effect - Wikipedia

    en.wikipedia.org/wiki/Evelyn_effect

    It then appears that the reaction proceeds mainly by a trans mechanism and, following the Zaitsev rule, 1-methylcyclohexene is preferentially formed in the early stages of the reaction. Indeed, if only about 10% of the total distillate is collected as the first fraction, one finds that the alkene is about 93% l-methylcyclohexene: at the end of ...

  7. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Cyclohexene is a hydrocarbon with the formula (CH 2) 4 C 2 H 2. It is an example of a cycloalkene. At room temperature, cyclohexene is a colorless liquid with a sharp odor. Among its uses, it is an intermediate in the commercial synthesis of nylon. [3]

  8. Methylenecyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylenecyclohexane

    This page was last edited on 20 September 2022, at 17:21 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  9. 3-Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/3-Methylcyclohexene

    3-Methylcyclohexene an organic compound consisting of cyclohexene with a methyl group substituent adjacent to the alkene group. Two other structural isomers are known: 1-methylcyclohexene and 4-methylcyclohexene. All are colorless volatile liquids classified as a cyclic olefins. They are specialized reagents.