Concept explainers
(a)
Interpretation:
The structure of the carboxylic acid that can be reacted with diazomethane to form the given methyl ester is to be drawn.
Concept introduction:
Methyl esters can be prepared from the carboxylic acid when reacted with diazomethane. The negatively charged oxygen of the carboxylate ion formed by deprotonation of carboxylic acid acts as a nucleophile. The carbon atom of diazomethane is converted to an electron-poor site by protonation. The reaction proceeds via
(b)
Interpretation:
The structure of the carboxylic acid that can be reacted with diazomethane to form the given methyl ester is to be drawn.
Concept introduction:
Methyl esters can be prepared from the carboxylic acid when reacted with diazomethane. The negatively charged oxygen of the carboxylate ion formed by deprotonation of carboxylic acid acts as a nucleophile. The carbon atom of diazomethane is converted to an electron-poor site by protonation. The reaction proceeds via
(c)
Interpretation:
The structure of the carboxylic acid that can be reacted with diazomethane to form the given methyl ester is to be drawn.
Concept introduction:
Methyl esters can be prepared from the carboxylic acid when reacted with diazomethane. The negatively charged oxygen of the carboxylate ion formed by deprotonation of carboxylic acid acts as a nucleophile. The carbon atom of diazomethane is converted to an electron-poor site by protonation. The reaction proceeds via
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ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
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- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning