Q8. [6] When Claisen products are heated in the presence of acid, they often undergo another reaction. Propose a complete mechanism for the reaction below (ester hydrolysis followed by thermal decarboxylation followed by keto-enol tautomerism). MS. H₂O*, heat OH D
Q8. [6] When Claisen products are heated in the presence of acid, they often undergo another reaction. Propose a complete mechanism for the reaction below (ester hydrolysis followed by thermal decarboxylation followed by keto-enol tautomerism). MS. H₂O*, heat OH D
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![Q8. [6] When Claisen products are heated in the presence of acid, they often undergo another reaction.
Propose a complete mechanism for the reaction below (ester hydrolysis followed by thermal decarboxylation
followed by keto-enol tautomerism).
SS.
H₂O*, heat
OH](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fbfa88dff-ad52-4b1c-8dff-1ce44d4d0dd5%2Fa72188b3-2bd7-410a-9308-28c3b2eb234e%2Fdipjmlp_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Q8. [6] When Claisen products are heated in the presence of acid, they often undergo another reaction.
Propose a complete mechanism for the reaction below (ester hydrolysis followed by thermal decarboxylation
followed by keto-enol tautomerism).
SS.
H₂O*, heat
OH
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