Search results
Results from the WOW.Com Content Network
This latter cumene converts into cumene radical and feeds back into subsequent chain formations of cumene hydroperoxides. A pressure of 5 atm is used to ensure that the unstable peroxide is kept in liquid state. Cumene hydroperoxide undergoes a rearrangement reaction in an acidic medium (the Hock rearrangement) to give phenol and acetone. In ...
It is a flammable colorless liquid that has a boiling point of 152 °C. Nearly all the cumene that is produced as a pure compound on an industrial scale is converted to cumene hydroperoxide, which is an intermediate in the synthesis of other industrially important chemicals, primarily phenol and acetone (known as the cumene process).
In commercial applications, the alkylating agents are generally alkenes, some of the largest scale reactions practiced in industry.Such alkylations are of major industrial importance, e.g. for the production of ethylbenzene, the precursor to polystyrene, from benzene and ethylene and for the production of cumene from benzene and propene in cumene process:
Most of those methods, but not all, involve the use of a solvent either for liquid-liquid extraction or extractive distillation. Many different solvents are suitable, including sulfolane (C 4 H 8 O 2 S), furfural (C 5 H 4 O 2 ), tetraethylene glycol (C 8 H 18 O 5 ), dimethylsulfoxide (C 2 H 6 OS), and N-methyl-2-pyrrolidone (C 5 H 9 NO).
1,2,4-Trimethylbenzene, also known as pseudocumene, is an organic compound with the chemical formula C 6 H 3 (CH 3) 3.Classified as an aromatic hydrocarbon, it is a flammable colorless liquid with a strong odor.
Cumene hydroperoxide is the organic compound with the formula C 6 H 5 C(CH 3) 2 OOH; this oily liquid is classified as an organic hydroperoxide. [2] Products of decomposition of cumene hydroperoxide are methylstyrene, acetophenone, and 2-phenylpropan-2-ol. [3] It is produced by treatment of cumene with oxygen, an autoxidation.
n-Propylbenzene is an aromatic hydrocarbon with the formula C 6 H 5 CH 2 CH 2 CH 3.The molecule consists of a propyl group attached to a phenyl ring. It is a colorless liquid. A more common structural isomer of this compound is cumene.
The DETAL process involving dehydrogenation of n-paraffins to olefins, and subsequent reaction with benzene using a fixed bed catalyst. This is newer technology and has several of the stages depicted in the HF/n-paraffins process, but it is principally different in the benzene alkylation step, during which a solid-state catalyst is employed.