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  2. Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexene

    1-Methylcyclohexene; 3-Methylcyclohexene; 4-Methylcyclohexene This page was last edited on 18 November 2024, at 14:45 (UTC). Text is available under the ...

  3. 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.

  4. 1-Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/1-Methylcyclohexene

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

  5. Evelyn effect - Wikipedia

    en.wikipedia.org/wiki/Evelyn_effect

    For these two reactions, there are 3 possible products, 3-methyl-cyclohexene,1-methyl-cyclohexene, methylene-cyclohexane. The production of each of these occurs at different rates and the ratios of these also change over time. It is well known that the dehydration of the cis isomer is 30 times faster than the trans isomer.

  6. Methylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexane

    CH 3 C 6 H 5 + 3 H 2 → CH 3 C 6 H 11. Methylcyclohexane, as a component of a mixture, is usually dehydrogenated to toluene, which increases the octane rating of gasoline. [4] The conversion of methylcyclohexane to toluene is a classic aromatization reaction. This platinum (Pt)-catalyzed process is practiced on scale in the production 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. 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. All are colorless volatile liquids classified as a cyclic olefins. They are specialized reagents.

  9. Cyclohexa-1,3-diene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexa-1,3-diene

    Cyclohexa-1,3-diene is an organic compound with the formula (C 2 H 4)(CH) 4. It is a colorless, flammable liquid. It is a colorless, flammable liquid. Its refractive index is 1.475 (20 °C, D).

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