Select the correct decreasing order of acid s | vedclass

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(C) $1$. Acid strength depends on the stability of the conjugate base formed after the loss of a proton $(H^+)$.$2$. $p-Nitrophenol$ $(d)$ is the stro

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$d > c > a > b$

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(C) $1$. Acid strength depends on the stability of the conjugate base formed after the loss of a proton $(H^+)$.$2$. $p-Nitrophenol$ $(d)$ is the strongest acid because the $-NO_2$ group exerts a strong $-I$ and $-M$ effect, which stabilizes the phenoxide ion significantly.$3$. $Phenol$ $(c)$ is more acidic than alcohols because the phenoxide ion is stabilized by resonance.$4$. Among alcohols, $Ethanol$ $(a)$ is more acidic than $2-Methylpropan-2-ol$ $(b)$ because the electron-donating inductive effect $(+I)$ of the three methyl groups in $2-Methylpropan-2-ol$ destabilizes the alkoxide ion more than the single methyl group in $Ethanol$.$5$. Thus, the decreasing order of acid strength is $d > c > a > b$.

Select the correct decreasing order of acid strength for the following compounds: $(a)$ $Ethanol$ $(b)$ $2-Methylpropan-2-ol$ $(c)$ $Phenol$ $(d)$ $p-Nitrophenol$.

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