Which of the following is the correct order o | vedclass

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(C) The acidic strength depends on the stability of the conjugate base formed after the loss of a proton $(H^+)$.$1$. Benzoic acid $(II)$ and $p$-Tolu

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$II > III > I > IV$

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(C) The acidic strength depends on the stability of the conjugate base formed after the loss of a proton $(H^+)$.$1$. Benzoic acid $(II)$ and $p$-Toluic acid $(III)$ are carboxylic acids,which are generally much stronger acids than phenols ($I$ and $IV$).$2$. Between $II$ and $III$,$p$-Toluic acid $(III)$ has a methyl group $(-CH_3)$ at the $p$-position,which is an electron-donating group ($+I$ effect),decreasing the acidity compared to benzoic acid $(II)$. Thus,$II > III$.$3$. Between $p$-Nitrophenol $(I)$ and $p$-Cresol $(IV)$,$p$-Nitrophenol $(I)$ has a strong electron-withdrawing group $(-NO_2)$,which stabilizes the phenoxide ion,making it more acidic than $p$-Cresol $(IV)$,which has an electron-donating methyl group $(-CH_3)$. Thus,$I > IV$.$4$. Comparing all,the order is $II > III > I > IV$.

Which of the following is the correct order of acidic strength for the given compounds?
$I$: $p$-Nitrophenol
$II$: Benzoic acid
$III$: $p$-Toluic acid
$IV$: $p$-Cresol

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Which of the following is the correct order of acidic strength for the given compounds?$I$: $p$-Nitrophenol$II$: Benzoic acid$III$: $p$-Toluic acid$IV$: $p$-Cresol