Chapter 22: Q68P-D (page 1204)
Question:Show how you would use an aldol, Claisen, or another type of condensation to make each compound
d.

Short Answer
Answer

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Chapter 22: Q68P-D (page 1204)
Question:Show how you would use an aldol, Claisen, or another type of condensation to make each compound
d.

Answer

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Show how you would use the acetoacetic ester synthesis to make the following compounds

Write equations showing the expected products of the following enamine alkylation and acylation reactions. Then give the final products expected after hydrolysis of the iminium salts.
(a) pyrrolidine enamine of pentan-3-one + allyl chloride
(b) pyrrolidine enamine of acetophenone + butanoyl chloride
(c) piperidine enamine of cyclopentanone + methyl iodide
(d) piperidine enamine of cyclopentanone + methyl vinyl ketone
The following compound results from base-catalyzed aldol cyclization of a 2-substituted cyclohexanone.

Show how you would use an aldol, Claisen, or another type of condensation to make each compound.

When propionaldehyde is warmed with sodium hydroxide, one of the products is 2-methylpent-2-enal. Propose a mechanism for this reaction.
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