What is the order of the decreasing reactivity for the carboxylic acid derivatives given above, in a nucleophilic substitution reaction?
II, IV, I, III
I, II, III, IV
IV, I, II, III
III, IV, I, II
A
III, IV, I, II
B
IV, I, II, III
C
II, IV, I, III
D
I, II, III, IV
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Solution
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Acid chloride is the most reactive followed by acid anhydride, then ester and amide is the most stable acid derivative. So, the order is as given above :
Hence, the correct option is A.
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