Show how would you accomplish the following synthetic conversions by adding an organolithium reagent to an acid. (a) COOH (b) Br (c) pentanoic acid - heptan-3-one (d) phenylacetic acid 3,3-dimethyl-1-phenylbutan-2-one

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter11: Reactions Of Alkyl Halides: Nucleophilic Substitutions And Eliminations
Section11.SE: Something Extra
Problem 35MP: One step in the urea cycle for ridding the body of ammonia is the conversion of argininosuccinate to...
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Show how would you accomplish the following synthetic conversions by adding an
organolithium reagent to an acid.
(a)
COOH
(b)
Br
(c) pentanoic acid - heptan-3-one
(d) phenylacetic acid 3,3-dimethyl-1-phenylbutan-2-one
Transcribed Image Text:Show how would you accomplish the following synthetic conversions by adding an organolithium reagent to an acid. (a) COOH (b) Br (c) pentanoic acid - heptan-3-one (d) phenylacetic acid 3,3-dimethyl-1-phenylbutan-2-one
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