Which of the following combination has the slowest esterification reaction rate? 1. CH3CH2CH2COOH IL (CH3)2CHCOOH I. CH3CH2CH2CH2CH2OH IV. (CH3)3CCH2OH II & II O 1& II O 1& IV O I & IV O 1& 1 O & IV

Organic Chemistry
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ISBN:9781305080485
Author:John E. McMurry
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Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions
Section19.SE: Something Extra
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QUESTION 18
Which of the following combination has the slowest esterification reaction rate?
1. CH3CH2CH2COOH
IL (CH3)2CHCOOH
II. CH3CH2CH2CH2CH20H
IV. (CH3)3CCH20H
O I & II
O1& IV
O & IV
O 1 & V
Transcribed Image Text:QUESTION 18 Which of the following combination has the slowest esterification reaction rate? 1. CH3CH2CH2COOH IL (CH3)2CHCOOH II. CH3CH2CH2CH2CH20H IV. (CH3)3CCH20H O I & II O1& IV O & IV O 1 & V
QUESTION 17
Which of the following is the correct order of mechanism steps for Fischer esterification?
[3] Protonation of one hydroxyl group in the intermediate by acid
[b] Protonation on carboxylic acid
a Hydrogen connected to the alcohol oxygen deprotonated by another alcohol
[d) Nucieophilic attack on the protonated carboxylic acid by an alcohol
re) Deprotonation by an alcohol
A Loss of protonated hydroxyl group as a water molecule & formation of carbon-oxygen double bond
[b]- (a)--(a]- [d] (d
(a] [b)-(- (d]- n-(e)
Transcribed Image Text:QUESTION 17 Which of the following is the correct order of mechanism steps for Fischer esterification? [3] Protonation of one hydroxyl group in the intermediate by acid [b] Protonation on carboxylic acid a Hydrogen connected to the alcohol oxygen deprotonated by another alcohol [d) Nucieophilic attack on the protonated carboxylic acid by an alcohol re) Deprotonation by an alcohol A Loss of protonated hydroxyl group as a water molecule & formation of carbon-oxygen double bond [b]- (a)--(a]- [d] (d (a] [b)-(- (d]- n-(e)
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