Between CH_3COOH and HCOOH,HCOOH will be: | vedclass

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Question

(C) The acidity of carboxylic acids depends on the stability of the carboxylate ion formed after the loss of a proton. In $CH_3COOH$,the methyl group

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More acidic

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(C) The acidity of carboxylic acids depends on the stability of the carboxylate ion formed after the loss of a proton. In $CH_3COOH$,the methyl group $(-CH_3)$ exerts a positive inductive effect ($+I$ effect),which increases the electron density on the carboxylate group,thereby destabilizing the conjugate base and decreasing acidity. In $HCOOH$,there is only a hydrogen atom attached to the carboxyl group,which does not exert any $+I$ effect. Therefore,$HCOOH$ is more acidic than $CH_3COOH$.

Between $CH_3COOH$ and $HCOOH$,$HCOOH$ will be:

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