m CPBA/H2O

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Take 1-methylcyclohexene as the alkene and treat it with the reagent.

The image displays a chemical reaction involving a reactant, cyclohexene, represented by a hexagonal ring with a double bond. The reaction condition is specified as "mCPBA/H₂O," which indicates the use of meta-Chloroperoxybenzoic acid (mCPBA) and water. An arrow points to the right, suggesting the production of a reaction product typically present in such chemical equations. However, the product isn't shown in this image. 

In this context, mCPBA is a common reagent for epoxidation reactions, where cyclohexene is likely converted into an epoxide in the presence of mCPBA and water. Epoxidation involves the formation of an epoxide ring by the addition of an oxygen atom across the double bond of cyclohexene.
Transcribed Image Text:The image displays a chemical reaction involving a reactant, cyclohexene, represented by a hexagonal ring with a double bond. The reaction condition is specified as "mCPBA/H₂O," which indicates the use of meta-Chloroperoxybenzoic acid (mCPBA) and water. An arrow points to the right, suggesting the production of a reaction product typically present in such chemical equations. However, the product isn't shown in this image. In this context, mCPBA is a common reagent for epoxidation reactions, where cyclohexene is likely converted into an epoxide in the presence of mCPBA and water. Epoxidation involves the formation of an epoxide ring by the addition of an oxygen atom across the double bond of cyclohexene.
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