Most acidic alcohol out of the following comp | vedclass

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Question

(C) The acidity of alcohols depends on the stability of the conjugate base (alkoxide ion) formed after the loss of a proton $(H^+)$.Electron-donating

Vedclass · Accepted Answer

$CH_3OH$

Vedclass · Answer

(C) The acidity of alcohols depends on the stability of the conjugate base (alkoxide ion) formed after the loss of a proton $(H^+)$.Electron-donating groups (like alkyl groups) destabilize the alkoxide ion by increasing the negative charge density,thereby decreasing acidity.In $(CH_3)_3COH$ (tert-butyl alcohol),there are three electron-donating methyl groups,making it the least acidic.In $CH_3CH_2OH$ (ethanol),there is one ethyl group.In $CH_3OH$ (methanol),there is no alkyl group attached to the carbon bearing the $-OH$ group.Comparing the aliphatic alcohols,$CH_3OH$ is the most acidic due to the absence of electron-donating alkyl groups.Note: $PhOH$ (phenol) is more acidic than aliphatic alcohols,but the question specifically asks for the most acidic 'alcohol'. Phenol is classified as a phenol,not an alcohol.

Most acidic alcohol out of the following compounds is

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