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
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Question
Propose a suitable synthesis

Transcribed Image Text:This image illustrates a chemical reaction involving the transformation of cyclohexene into cyclohexanone.
On the left, the structure of cyclohexene is depicted as a six-membered carbon ring with one double bond.
An arrow pointing to the right indicates a chemical reaction or transformation.
On the right, the structure of cyclohexanone is shown. It is also a six-membered carbon ring, but it features a ketone functional group (C=O) attached to one of the carbon atoms, indicating the presence of an oxygen atom double-bonded to the carbon atom in the ring. Additionally, a hydrogen atom (H) is bonded to the oxygen, completing the conversion to cyclohexanone.
This reaction is likely an oxidation process where cyclohexene is oxidized to form cyclohexanone.
Expert Solution

Step 1
-> Alkene has nucleophilic character hence it can give electrophilic addition reaction. In presence of Acid first of all carbocation formed and reaction proceeds through most stable carbocation.
-> Alkyl halide form Grignard reagent and can give nucleophilic addition reaction to carbonyl center.
-> PCC can oxidize alcohol to carbonyl compound.
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