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  2. 1-Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/1-Methylcyclohexene

    Oxidation of 1-methylcyclohexene catalyzed by cytochrome P450 yields a 2:1 mixture of hydroxylation to epoxidation products. [4] The stereochemistry of hydroformylation has been examined using 1-methylcyclohexene. The main product has the formyl group on the less substituted alkene-carbon, trans with respect to the methyl substituent.

  3. Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexene

    Download as PDF; Printable version; In other projects ... move to sidebar hide. Methylcyclohexene can refer to any of three compounds: 1-Methylcyclohexene; 3 ...

  4. 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 .

  5. 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.

  6. Methylenecyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylenecyclohexane

    Download as PDF; Printable version; ... [1] [2] [3] It can also be synthesized as a side product of the dehydration of 2-methylcyclohexanol into 1-methylcyclohexene.

  7. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  8. Cyclohexenone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexenone

    Cyclohexenone is an organic compound which is a versatile intermediate used in the synthesis of a variety of chemical products such as pharmaceuticals and fragrances. [2] It is colorless liquid, but commercial samples are often yellow.

  9. 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 ...