Identify the product of Cummene-Peroxide reaction among the following.
A.Phenol + Acetaldehyde
B.Phenol + Acetone
C.Ethanol + Acetaldehyde
D.Ethanol + Acetone
Answer
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Hint:The given reaction is Cumene-Peroxide rearrangement. It is a very important method in organic chemistry used for the preparation of phenol. Cumene is known as isopropyl benzene. Cumene-hydroperoxide is used as a polymerization initiator and for the synthesis of acetone and phenol.
Complete step by step answer:
As we know the starting material is benzene hydroperoxide.
The first step is the formation of benzene peroxide from cumene
Here, cumene on adding oxygen forms cumene hydroperoxide.
The tertiary hydroperoxide undergoes rearrangement in an acidic medium.
When cumene hydroperoxide is hydrolyzed in an acidic medium. This is known as Hock Rearrangement.
In the first step, the terminal hydroperoxy Oxygen atom will be protonated.
In the second step, the phenyl group then migrates from the benzyl carbon to the adjacent oxygen atom. It will further provide a resonance stabilized tertiary carbocation.
This is known as Baeyer- Villiger oxidation.
In this reaction, the carbocations are attacked by water and a proton is transferred from oxygen to the ether O. The ion then gives phenol and acetone.
Therefore, the product of Cumene- hydroperoxide rearrangement reaction is acetone and phenol.
Hence, the correct option is (B).
Note: The Cumene-peroxide rearrangement or Hock rearrangement is used for the preparation of phenol. On decomposing cumene hydroperoxide, we get methyl styrene, acetophenone, and cumy alcohol. If the isopropyl benzene or the cumene is replaced with cyclohexyl benzene, it cleaves to give phenol and cyclohexanone. It is used as a precursor for the synthesis of nylon. 2-naphthol can by a method analogous to the Cumene process.
Complete step by step answer:
As we know the starting material is benzene hydroperoxide.
The first step is the formation of benzene peroxide from cumene
Here, cumene on adding oxygen forms cumene hydroperoxide.
The tertiary hydroperoxide undergoes rearrangement in an acidic medium.
When cumene hydroperoxide is hydrolyzed in an acidic medium. This is known as Hock Rearrangement.
In the first step, the terminal hydroperoxy Oxygen atom will be protonated.
In the second step, the phenyl group then migrates from the benzyl carbon to the adjacent oxygen atom. It will further provide a resonance stabilized tertiary carbocation.
This is known as Baeyer- Villiger oxidation.
In this reaction, the carbocations are attacked by water and a proton is transferred from oxygen to the ether O. The ion then gives phenol and acetone.
Therefore, the product of Cumene- hydroperoxide rearrangement reaction is acetone and phenol.
Hence, the correct option is (B).
Note: The Cumene-peroxide rearrangement or Hock rearrangement is used for the preparation of phenol. On decomposing cumene hydroperoxide, we get methyl styrene, acetophenone, and cumy alcohol. If the isopropyl benzene or the cumene is replaced with cyclohexyl benzene, it cleaves to give phenol and cyclohexanone. It is used as a precursor for the synthesis of nylon. 2-naphthol can by a method analogous to the Cumene process.
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