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  2. 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.

  3. 1-Ethynylcyclohexanol - Wikipedia

    en.wikipedia.org/wiki/1-Ethynylcyclohexanol

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  4. Ethylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Ethylcyclohexane

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  5. 2-Ethylhexanol - Wikipedia

    en.wikipedia.org/wiki/2-Ethylhexanol

    2-Ethylhexanol (abbreviated 2-EH) is an organic compound with the chemical formula C H 3 CH 2 CH 2 CH 2 CH(CH 2 CH 3)CH 2 OH.It is a branched, eight-carbon chiral alcohol.It is a colorless liquid that is poorly soluble in water but soluble in most organic solvents.

  6. 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.

  7. Evelyn effect - Wikipedia

    en.wikipedia.org/wiki/Evelyn_effect

    The Evelyn effect is defined as the phenomena in which the product ratios in a chemical reaction change as the reaction proceeds. This phenomenon contradicts the fundamental principle in organic chemistry by reactions always go by the lowest energy pathway.

  8. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

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  9. Hydration reaction - Wikipedia

    en.wikipedia.org/wiki/Hydration_reaction

    The general chemical equation for the hydration of alkenes is the following: . RRC=CH 2 + H 2 O → RRC(OH)-CH 3. A hydroxyl group (OH −) attaches to one carbon of the double bond, and a proton (H +) adds to the other.