Which of the following structures would not be a legitmate intermediate for the mechanism of the ischer estenitication shown belo? H2SO, CH,OH OCH3 H20 OCH3 OH O OH OH OCH3 HO. OCH, ÓCH3 A B D

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter23: Carbonyl Condensation Reactions
Section23.SE: Something Extra
Problem 24VC
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Which of the following structures would not be a legitmate intermediate for the mechanism of the ischer esteritication shown below?
H2SO4
CH,OH
OCH3
H20
OCH3
он
он
он
OH
OCH3
OH
OCH3
ÓCH3
A
C
D
Transcribed Image Text:Which of the following structures would not be a legitmate intermediate for the mechanism of the ischer esteritication shown below? H2SO4 CH,OH OCH3 H20 OCH3 он он он OH OCH3 OH OCH3 ÓCH3 A C D
Question 23
Which of the folowing carborylic acid derivatives has the fastest rate of hydrolysis to give acetic acid (e, is most reactivey?
CH3
NH2
CH3
CI
CH3
CH3
CH3
OCH2CH3
Transcribed Image Text:Question 23 Which of the folowing carborylic acid derivatives has the fastest rate of hydrolysis to give acetic acid (e, is most reactivey? CH3 NH2 CH3 CI CH3 CH3 CH3 OCH2CH3
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