Which of the following has the most acidic pr | vedclass

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(D) The acidity of a proton depends on the stability of the conjugate base formed after the removal of the proton. In $(CH_3CO)_3CH$,the central carbo

Vedclass · Accepted Answer

$(CH_3CO)_3CH$

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(D) The acidity of a proton depends on the stability of the conjugate base formed after the removal of the proton. In $(CH_3CO)_3CH$,the central carbon is attached to three electron-withdrawing acetyl groups $(-COCH_3)$. Upon removal of the proton,the resulting carbanion is stabilized by resonance across three carbonyl groups,making it the most stable conjugate base among the given options. Therefore,$(CH_3CO)_3CH$ has the most acidic proton.

Which of the following has the most acidic proton?

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