Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
Problem 26MP: Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium...
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Give clear detailed mechanism Solution with explanation needed..don't give Handwritten answer
![What is the major organic product for the reaction below:
H₂
Lindlar Catalyst
CH3CH₂C=CCH3
H3CH₂C
H
H₂CH₂C
H₂C
H
H
K
H
H
CH3
CH3
CH3
O CH3CH2CH2CH2CH3](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb1b4a131-f1e9-4058-89f3-f58de2b8b968%2Fec6ea864-33ce-4d31-bc54-ffb3f676baf9%2Fvzri9s8_processed.png&w=3840&q=75)
Transcribed Image Text:What is the major organic product for the reaction below:
H₂
Lindlar Catalyst
CH3CH₂C=CCH3
H3CH₂C
H
H₂CH₂C
H₂C
H
H
K
H
H
CH3
CH3
CH3
O CH3CH2CH2CH2CH3
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