The correct order of increasing acidic streng | vedclass

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Question

(C) The correct order of increasing acidic strength is: $	ext{ethanol} < 	ext{phenol} < 	ext{acetic acid} < 	ext{chloroacetic acid}$.$1$. $	ext{E

Vedclass · Accepted Answer

ethanol $ < $ phenol $ < $ acetic acid $ < $ chloroacetic acid

Vedclass · Answer

(C) The correct order of increasing acidic strength is: $	ext{ethanol} $1$. $	ext{Ethanol}$ is the least acidic among the given compounds.$2$. $	ext{Phenol}$ is more acidic than $	ext{ethanol}$ because the $	ext{phenoxide ion}$ formed after deprotonation is stabilized by resonance,whereas the $	ext{ethoxide ion}$ is not.$3$. $	ext{Carboxylic acids}$ are more acidic than $	ext{phenols}$ because the $	ext{carboxylate ion}$ is stabilized by two equivalent resonance structures.$4$. $	ext{Chloroacetic acid}$ $(ClCH_2COOH)$ is more acidic than $	ext{acetic acid}$ $(CH_3COOH)$ due to the strong electron-withdrawing inductive effect ($-I$ effect) of the $	ext{chlorine}$ atom,which stabilizes the $	ext{carboxylate anion}$.Therefore,the correct option is $(C)$.

The correct order of increasing acidic strength among the following is:

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