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Chapter 23: Q7P (page 761)

Show how you would synthesize the following compound using an aldol reaction:

Short Answer

Expert verified

The name of the given compound is: Cyclopropyl Acetaldehyde.

Step by step solution

Formation of Compound

For the formation of this compound through aldol reaction we must have aldehyde having 1 cyclopropyl ring with at least 1𝛂-hydrogen atom.

Chemical Reaction:

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Most popular questions from this chapter

What product would you obtain from a base-catalyzed Michael reaction of 3-buten-2-one with each of the following nucleophilic donors?

The third and fourth steps in the synthesis of Hagemann’s ester from ethyl acetoacetate and formaldehyde (Problem 23-71) are an intramolecular aldol cyclization to yield a substituted cyclohexenone, and a decarboxylation reaction. Write both reactions, and show the products of each step.

Show how you might use an enamine reaction to prepare each of the following compounds: