d) Outline a Wittig synthesis of 3-methylhex-3-ene. f) Show all the steps in the synthesis of 3-butyl-2-heptanone starting with ethylacetoacetate as one of the reagents. g) Give an example of the use of enamines in organic synthesis.

d) Outline a Wittig synthesis of 3-methylhex-3-ene. f) Show all the steps in the synthesis of 3-butyl-2-heptanone starting with ethylacetoacetate as one of the reagents. g) Give an example of the use of enamines in organic synthesis.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter17: Carboxylic Acids

Section: Chapter Questions

Problem 17.23P

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all mechanism should be shown

d) Outline a Wittig synthesis of 3-methylhex-3-ene.
f) Show all the steps in the synthesis of 3-butyl-2-heptanone starting with
ethylacetoacetate as one of the reagents.
g) Give an example of the use of enamines in organic synthesis.

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