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1. OH R-C-R + R-MgX R CI R 2. -CH=CH-CH3 -CH=CH-CH2 base

1. OH R-C-R + R-MgX R CI R 2. -CH=CH-CH3 -CH=CH-CH2 base

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter22: Organic And Biological Molecules
Section: Chapter Questions
Problem 176MP
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For 1 and 2, provide a mechanistic explanation for the following observation: 1. Acid chlorides undergo reaction with Grignard reagents at room temperature to form a tertiary alcohol. 2. Treatment of an α,β-unsaturated carbonyl compound with a base yields an anion by removal of H+ from the γ carbon. Why are the hydrogens on this carbon acidic?
1. OH R-C-R + R-MgX R CI R
Transcribed Image Text:1. OH R-C-R + R-MgX R CI R
2. -CH=CH-CH3 -CH=CH-CH2 base
Transcribed Image Text:2. -CH=CH-CH3 -CH=CH-CH2 base
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