enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. Baeyer–Villiger oxidation - Wikipedia

    en.wikipedia.org/wiki/Baeyer–Villiger_oxidation

    The Baeyer–Villiger oxidation is an organic reaction that forms an ester from a ketone or a lactone from a cyclic ketone, using peroxyacids or peroxides as the oxidant. [1] The reaction is named after Adolf von Baeyer and Victor Villiger who first reported the reaction in 1899. [1] Baeyer-Villiger oxidation

  4. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    The oxidation of primary alcohols to carboxylic acids can be carried out using a variety of reagents, but O 2 /air and nitric acid dominate as the oxidants on a commercial scale. Large scale oxidations of this type are used for the conversion of cyclohexanol alone or as a mixture with cyclohexanone to adipic acid .

  5. 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.

  6. Adipic acid - Wikipedia

    en.wikipedia.org/wiki/Adipic_acid

    Adipic acid is produced by oxidation of a mixture of cyclohexanone and cyclohexanol, which is called KA oil, an abbreviation of ketone-alcohol oil. Nitric acid is the oxidant. The pathway is multistep. Early in the reaction, the cyclohexanol is converted to the ketone, releasing nitrous acid:

  7. 1,2-Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/1,2-Cyclohexanedione

    It is a colorless compound that is soluble in a variety of organic solvents. It can be prepared by oxidation of cyclohexanone by selenium dioxide. [1] The enol is about 1 kcal/mol more stable than the diketo form. [2] Numerous diimine and dioxime ligands have been prepared from this diketone. [1] It also condenses with 1,2-diamines to give ...

  8. Cyclohexanone monooxygenase - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone_monooxygenase

    Cyclohexanone monooxygenase is one of the most prominent Baeyer-Villiger monooxygenases (BVMOs) and has a low substrate specificity, allowing it to catalyze a number of reactions; given the variety of substrates, cyclohexanone monooxygenase is a useful enzyme for industrial applications.

  9. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Although rather unreactive, cyclohexane undergoes autoxidation to give a mixture of cyclohexanone and cyclohexanol. The cyclohexanone–cyclohexanol mixture, called "KA oil", is a raw material for adipic acid and caprolactam, precursors to nylon. Several million kilograms of cyclohexanone and cyclohexanol are produced annually. [9]