Among the tertiary alcohols shown below, which one cannot be synthesized by reacting an appropriate Grignard reagent with an ester? CH2CH3 H3C-C-OH CH3 CH3 H3C-C-OH CH3 CH2CH3 H3C-C-OH ČH2CH3 CH2CH3 Нас -с-он CH(CH3)2 CH(CH3)2 H3C-C-OH CH(CH3)2

Among the tertiary alcohols shown below, which one cannot be synthesized by reacting an appropriate Grignard reagent with an ester? CH2CH3 H3C-C-OH CH3 CH3 H3C-C-OH CH3 CH2CH3 H3C-C-OH ČH2CH3 CH2CH3 Нас -с-он CH(CH3)2 CH(CH3)2 H3C-C-OH CH(CH3)2

EBK A SMALL SCALE APPROACH TO ORGANIC L

4th Edition

ISBN:9781305446021

Author:Lampman

Publisher:Lampman

Chapter22: 4-methylcyclohexene

Section: Chapter Questions

Problem 2Q

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Concept explainers

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

Question

Among the tertiary alcohols shown below, which one cannot be synthesized
by reacting an appropriate Grignard reagent with an ester?
CH2CH3
H3C-C-OH
CH3
CH3
H3C-C-OH
CH3
CH2CH3
H3C-C-OH
CH2CH3
CH,CH3
H3C-C-OH
CH(CH3)2
CH(CH3)2
H3C-C-OH
CH(CH3)2

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