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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.
1 Material Safety Data Sheet. 2 Structure and properties. 3 Thermodynamic properties. ... Download as PDF; Printable version; In other projects Wikidata item; Appearance.
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 ...
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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 ...
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Cyclohexanehexone, also known as hexaketocyclohexane and triquinoyl, is an organic compound with formula C 6 O 6, the sixfold ketone of cyclohexane.It is an oxide of carbon (an oxocarbon), a hexamer of carbon monoxide.
Cyclohexylbenzene is a precursor to both phenol and cyclohexanone. [7] Hydration of cyclohexene gives cyclohexanol, which can be dehydrogenated to give cyclohexanone, a precursor to caprolactam. [8] The oxidative cleavage of cyclohexene gives adipic acid. Hydrogen peroxide is used as the oxidant in the presence of a tungsten catalyst. [9]