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

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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 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
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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