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Chapter 23: Q23-7P (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

Step 1:

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

The following structure represents an intermediate formed by the addition of an ester enolate ion to a second ester molecule. Identify the reactant, the leaving group, and the product.

Aldol condensation of 3-methyl cyclohexanone leads to a mixture of two enone products, not counting double-bond isomers. Draw them.

The following reactions are unlikely to provide the indicated product in high yield. What is wrong with each?

What product would you expect to obtain from aldol cyclization of hexanedial, $O H C C H_{2} C H_{2} C H_{2} C H_{2} C H O$

The following reaction involves two successive intramolecular Michael reactions. Write both steps, and show their mechanisms.

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

Short Answer

Step by step solution

Step 1:

chemical reaction:

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Most popular questions from this chapter

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