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  2. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    Cyclohexanol is the organic compound with the formula HOCH(CH 2) 5. The molecule is related to cyclohexane by replacement of one hydrogen atom by a hydroxyl group . [ 4 ] This compound exists as a deliquescent colorless solid with a camphor-like odor, which, when very pure, melts near room temperature.

  3. 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).

  4. Cyclohexane (data page) - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_(data_page)

    Liquid properties Std enthalpy change of formation, Δ f H o liquid –156.4 kJ/mol Standard molar entropy, S o liquid: 204 J/(mol K) Enthalpy of combustion, Δ c H o –3919.6 kJ/mol Heat capacity, c p: 156 J/(mol K) or 1.85 J/(g K) Gas properties Std enthalpy change of formation, Δ f H o gas –123.1 kJ/mol Standard molar entropy, S o gas ...

  5. Cyclohexanone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone

    Cyclohexanone is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [11]. C 6 H 12 + O 2 → (CH 2) 5 CO + H 2 O. This process forms cyclohexanol as a by-product, and this mixture, called "KA Oil" for ketone-alcohol oil, is the main feedstock for the production of adipic acid.

  6. Cyclohexane-1,2,3,4,5,6-hexol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane-1,2,3,4,5,6-hexol

    Cyclohexane-1,2,3,4,5,6-hexol is a family of chemical compounds with formula C 6 H 12 O 6, whose molecule consists of a ring of six carbon atoms, each bound to one hydrogen atom and one hydroxyl group (–OH). There are nine stereoisomers, that differ by the position of the hydroxyl groups relative to the mean plane of the ring.

  7. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    In another major industrial process, cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [10] 2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid, used to make nylon.

  8. 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]

  9. Cyclohexyl chloride - Wikipedia

    en.wikipedia.org/wiki/Cyclohexyl_chloride

    Cyclohexyl chloride (or chlorocyclohexane) is a chlorinated hydrocarbon with the formula (CH 2) 5 CHCl. It is a colorless liquid. Cyclohexyl chloride can be prepared from cyclohexanol by treatment with hydrogen chloride. [1]