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the Baeyer-Villiger oxidation of cyclohexyl meth

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Concepts and reason

The concepts used to solve this problem is based on Baeyer-Villiger oxidation.

Firstly, the chemical reaction of cyclohexyl methyl ketone with peroxy acid is written. After that, the formation of the product is explained by the mechanism.

Fundamentals

Baeyer-Villiger oxidation:

Baeyer-Villiger oxidation is an organic reaction that is used to convert ketone to an ester using a peroxy acid.

The reaction is illustrated as follows.

HO
R
.R2
R2
Ri
Peroxy acid
Ester
Ketone

The more electron rich migrate to the oxygen. The order is given as follows.

3- alkyl 2-alkyl> aryl>-alkyl > methyl

The chemical reaction of cyclohexyl methyl ketone with peroxy acids as follows.

CHз
C
НО
CH3
R
Peroxy acid
Су
cyclohexyl acetate
ketone

The mechanism for the formation of cyclohexyl acetate from the reaction cyclohexyl methyl ketone with a peroxy acid is shown below.

н
CH3
CHз
R
H
Н
.CH3
CH3
Н
CH3
R
.CH3
):
CH3
R
Н-О
cyclohexyl acetate
Product

Ans:

The main product formed from the Baeyer-Villiger oxidation of cyclohexyl methyl ketone is as follows.

CH3
cyclohexyl acetate

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the Baeyer-Villiger oxidation of cyclohexyl methyl ketone, shown below, draw the main organic product.
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