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Cyclohexylbenzene is the organic compound with the structural formula C 6 H 5 −C 6 H 11. It is a derivative of benzene with a cyclohexyl substituent (C 6 H 11 ). It is a colorless liquid.
Benzene is converted to cyclohexylbenzene by acid-catalyzed alkylation with cyclohexene. [6] 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.
C 12 H 9 N 3 O 4: azo violet: C 12 H 9 ClF 3 N 3 O: norflurazon: 27314-13-2 C 12 H 9 Cl 2 NO 3: vinclozoline: 50471-44-8 C 12 H 9 N: carbazole: 86-74-8 C 12 H 9 NO: phenoxazine: 135-67-1 C 12 H 9 NS: phenothiazine: 92-84-2 C 12 H 9 P
A route analogous to the cumene process begins with cyclohexylbenzene. It is oxidized to a hydroperoxide, akin to the production of cumene hydroperoxide. Via the Hock rearrangement, cyclohexylbenzene hydroperoxide cleaves to give phenol and cyclohexanone. Cyclohexanone is an important precursor to some nylons. [25]
Cyclohexylbenzene can replace isopropylbenzene. Via the Hock rearrangement, cyclohexylbenzene hydroperoxide cleaves to give phenol and cyclohexanone. Cyclohexanone is an important precursor to some nylons. [8] Starting with the alkylation of benzene with mixture of 1 and 2-butenes, the cumene process produces phenol and butanones. [5]
Alumnus Anudeep Revuri, 23, of New Brunswick, allegedly developed the closed network used by the group to sell narcotics to other Rutgers students.
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The State Department said an American teacher arrested in Russian on drug charges in 2021 has been designated by the U.S. government as wrongfully detained.