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![Draw a plausible mechanism for the following transformation:
[H2SO4]
excess EtOH
-H2O
EtO OEt](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F88a41c52-4f3e-4331-9ea2-65f8854095d8%2Ff93a7e38-4170-461f-a7d5-ba9e54e5400c%2Fxec6iof_processed.png&w=3840&q=75)
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- The Favorskii reaction involves treatment of an -bromo ketone with base to yield a ring-contracted product. For example, reaction of 2-bromocyclohexanone with aqueous NaOH yields cyclopentanecarboxylic acid. Propose a mechanism.Draw a plausible mechanism for the following transformation: [H2SO4] excess EtOH -H₂O EtO OEtPropoase a plausible mechanism for the following transformation: HO H [H3O*] EtOH
