Question 1

How would you prepare the following compound using an alkylation reaction?

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Question 2

Identify products a and
b.

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b.
 ...

Question 3

Predict the major aldol product of the following reaction.

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Question 4

Identify the intermediate imine that results from the following reaction.

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Question 5

When treated with base and heat, the following diketone undergoes an intramolecular aldol reaction followed by dehydration to produce cis-jasmone, a perfume component. Draw the structure of the product.

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Question 6

Draw the structure of the diastereomer that is formed preferentially in the following reaction:

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Quiz 17: Carbonyl Alpha-Substitution and Condensation Reactions

How would you prepare the following compound using an alkylation reaction?

Identify products a and b.

Predict the major aldol product of the following reaction.

Identify the intermediate imine that results from the following reaction.

When treated with base and heat, the following diketone undergoes an intramolecular aldol reaction followed by dehydration to produce cis-jasmone, a perfume component. Draw the structure of the product.

Draw the structure of the diastereomer that is formed preferentially in the following reaction: