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Chapter 22: Q69-E (page 1204)

Question: Predict the products of the following reactions

e.

Short Answer

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Answer

Step by step solution

01

Enamine alkylation

Enamine shows reaction under mild conditions they displace the halide from the alkyl halide for the formation of the alkylated iminium salt followed by hydrolysis to form an alkylated ketone.

02

Mechanism

  1. Enamine displaces halide
  2. Formation of alkylated iminium ion
  3. Hydrolysis
  4. Formation of alkylated ketone

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Most popular questions from this chapter

Show how you would accomplish the following conversions in good yields. You may use any necessary reagents.

Predict the products from this sequence of reactions

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

c.

The following compound results from base-catalyzed aldol cyclization of a 2-substituted cyclohexanone.

  1. Show the diketone that would cyclize to give this product.
  2. Propose a mechanism for the cyclization

Question: Predict the products of the following reactions

g.
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