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Alkene elements appear to be useful in generating a mCPBA reaction. A product of Alkene is cyclohexene because it is generally used as a solvent. When cyclohexane is added to mCPBA, it creates epoxide.

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What is the mechanism of the oxidation reaction between a ketone and MCPBA?

The oxidation reaction between a ketone and MCPBA involves the transfer of an oxygen atom from MCPBA to the ketone, resulting in the formation of an ester. This process is known as Baeyer-Villiger oxidation.


What is the mechanism of the Baeyer-Villiger oxidation reaction involving MCPBA?

In the Baeyer-Villiger oxidation reaction with MCPBA, a peracid like MCPBA reacts with a ketone or aldehyde to form an ester or lactone. This reaction involves the transfer of an oxygen atom from the peracid to the carbonyl group, resulting in the formation of a new bond between the oxygen and the carbon atom adjacent to the carbonyl group.


Why is it not possible to selectively epoxidize an alkene with mCPBA in the presence of a ketone?

It is not possible to selectively epoxidize an alkene with mCPBA in the presence of a ketone because mCPBA can react with both the alkene and the ketone, leading to non-selective reactions and the formation of undesired byproducts.


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