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  2. Methylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexane

    Methylcyclohexane (cyclohexylmethane) is an organic compound with the molecular formula is CH 3 C 6 H 11. Classified as saturated hydrocarbon , it is a colourless liquid with a faint odor. Methylcyclohexane is used as a solvent .

  3. Alkyl cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Alkyl_cycloalkane

    Alkyl cycloalkanes are chemical compounds with an alkyl group with a single ring of carbons to which hydrogens are attached according to the formula C n H 2n. They are named analogously to their normal alkane counterpart of the same carbon count: methylcyclopropane, methylcyclobutane, methylcyclopentane, methylcyclohexane, etc. [1]

  4. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    trans-1,3-Disubstituted cyclohexanes are like cis-1,2- and cis-1,4- and can flip between the two equivalent axial/equatorial forms. [ 2 ] Cis -1,4-Di- tert -butylcyclohexane has an axial tert -butyl group in the chair conformation and conversion to the twist-boat conformation places both groups in more favorable equatorial positions.

  5. 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 .

  6. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    A cycloalkyl group is derived from a cycloalkane by removal of a hydrogen atom from a ring and has the general formula −C n H 2n−1. [2] Typically an alkyl is a part of a larger molecule. In structural formulae, the symbol R is used to designate a generic (unspecified) alkyl group. The smallest alkyl group is methyl, with the formula −CH 3 ...

  7. 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. [5]

  8. Methylcyclohexanone - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexanone

    Methylcyclohexanones are a group of three isomers: 2-methylcyclohexanone, 3-methylcyclohexanone, and 4-methylcyclohexanone. [1] They can be viewed as derivative of cyclohexanone. They can be prepared by oxidation of methylcyclohexane as well as partial hydrogenation of the corresponding cresols. All are colorless liquids. The 2- and 3-isomers ...

  9. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Cyclohexane is a cycloalkane with the molecular formula C 6 H 12.Cyclohexane is non-polar.Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used).