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  2. 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.

  3. Cyclohexane (data page) - Wikipedia

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

    1 Material Safety Data Sheet. 2 Structure and properties. 3 Thermodynamic properties. 4 Vapor pressure of liquid. 5 Distillation data. 6 Spectral data. 7 References.

  4. Cyclohexanone oxime - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone_oxime

    Cyclohexanone oxime can be prepared from the condensation reaction between cyclohexanone and hydroxylamine: [1] C 5 H 10 CO + H 2 NOH → C 5 H 10 C=NOH + H 2 O. Alternatively, another industrial route involves the reaction of cyclohexane with nitrosyl chloride, which is a free-radical reaction. This method is advantageous as cyclohexane is ...

  5. Cyclohexenone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexenone

    It can be obtained from cyclohexanone by α-bromination followed by treatment with base. Hydrolysis of 3-chloro cyclohexene followed by oxidation of the cyclohexenol is yet another route. Cyclohexenone is produced industrially by catalytic oxidation of cyclohexene, for example with hydrogen peroxide and vanadium catalysts. Several patents ...

  6. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 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.

  7. Methylcyclohexanone - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexanone

    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 are chiral.

  8. Cycloheptanone - Wikipedia

    en.wikipedia.org/wiki/Cycloheptanone

    Cycloheptanone is also produced by the reaction of cyclohexanone with sodium ethoxide and nitromethane. The resulting sodium salt of 1-(nitromethyl)cyclohexanol is added to acetic acid and shaken with hydrogen gas in the presence of W-4 Raney nickel catalyst. Sodium nitrite and acetic acid are then added to give cycloheptanone. [5]

  9. 1-Ethynylcyclohexanol - Wikipedia

    en.wikipedia.org/wiki/1-Ethynylcyclohexanol

    Synthesis of 1-ethynylcyclohexanol from cyclohexanone. 1-Ethynylcyclohexanol can be prepared from cyclohexanone by the reacting it with sodium acetylide in liquid ammonia , followed by an acidic work-up .