Determine the product in the following conjugated addition reaction.

Show how the following products might be synthesized from suitable Michael donors and acceptors.

(e)

In Solved Problem 22-9, the target molecule was synthesized using a Michael addition to form the bond that is β,γ to the upper carbonyl group. Another approach is to use a Michael addition to form the bond that is β,γ to the other (lower) carbonyl group. Show how you would accomplish this alternative synthesis.

Show how cyclohexanone might be converted to the following δ-diketone (Hint: Stork).

Which of the following pairs of starting materials can be used to synthesize ${\mathrm{CH}}_3\mathrm{COCH}{2}_2\mathrm{CH}{2}_1\mathrm{COOEt}$ via a Michael addition reaction?

Determine the product in the following conjugated addition reaction.

Determine the product in the following conjugated addition reaction

What reagents should be used to prepare the following compounds?

b.