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B. Bonus (10 pts) Intramolecular Aldol... CH3

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Answer #1

Answer.

In order to find out the final product, we need to follow the following steps:

Step-1: Identify the  - carbon

1 and  2 are the  - carbons of the ketone group while  ' is the  - carbon of the aldehyde group.

With ring forming reactions, five and six membered rings are preferred and there is a possibility of ring formation if the attacking carbon is  2.

Step-2: An acid-base reaction

Hydroxide functions as a base and removes the acidic  - hydrogen bonded to the  - carbon and gives the reactive enolate.

Step-3: Nucleophilic attack

Answer In order to find out the final product, we need to follow the following steps: Step-1: Identify the O carbon CH CAH CH 2 3 2. α1 and α 2 are the α-carbons of the ketone group while α , is the α-carbon of the aldehyde group. With ring forming reactions, five and six membered rings are preferred and there is a possibility of ring formation if the attacking carbon is Step-2: An acid-base reaction CH OH C CHH 2

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