Give the relative rates of reaction of the four carboxylic acid derivatives below with methylamine to give an N-methyl amide. H3C OCH3 H3C CI H3C NH2 H3C CH3 a C d Most reactive 2nd most reactive 3rd most reactive Least reactive Give the relative rates of reaction of the four carboxylic acid derivatives below with aqueous sodium hydroxide to give the sodium carboxylate salt. གཅིག་ལྡན དང་ཅིག་ཡིས་སྡུད་པ་དངའི་ཟག་པ་དཀྱི Most reactive CH3 3 2nd most reactive 3rd most reactive Least reactive H3C NH2 H3C OH
Give the relative rates of reaction of the four carboxylic acid derivatives below with methylamine to give an N-methyl amide. H3C OCH3 H3C CI H3C NH2 H3C CH3 a C d Most reactive 2nd most reactive 3rd most reactive Least reactive Give the relative rates of reaction of the four carboxylic acid derivatives below with aqueous sodium hydroxide to give the sodium carboxylate salt. གཅིག་ལྡན དང་ཅིག་ཡིས་སྡུད་པ་དངའི་ཟག་པ་དཀྱི Most reactive CH3 3 2nd most reactive 3rd most reactive Least reactive H3C NH2 H3C OH
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
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:Give the relative rates of reaction of the four carboxylic acid derivatives below with methylamine to give an N-methyl amide.
H3C
OCH3
H3C
CI
H3C
NH2
H3C
CH3
a
C
d
Most reactive
2nd most reactive
3rd most reactive
Least reactive

Transcribed Image Text:Give the relative rates of reaction of the four carboxylic acid derivatives below with aqueous sodium hydroxide to give the
sodium carboxylate salt.
གཅིག་ལྡན དང་ཅིག་ཡིས་སྡུད་པ་དངའི་ཟག་པ་དཀྱི
Most reactive
CH3
3
2nd most reactive
3rd most reactive
Least reactive
H3C
NH2
H3C
OH
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