The decreasing order of nucleophilicity among the following nucleophiles is:
$(I)$ $CH_3-COO^{-}$
$(II)$ $CH_3O^{-}$
$(III)$ $C_6H_5O^{-}$
$(IV)$ $CH_3-SO_3^-$

  • A
    $I, II, III, IV$
  • B
    $IV, III, II, I$
  • C
    $II, III, I, IV$
  • D
    $III, II, I, IV$

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Similar Questions

Carboxylic acids contain a carbonyl group but do not show the nucleophilic addition reaction like aldehydes or ketones. Why?

The correct order of their reactivity towards hydrolysis at room temperature is:

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

The order of strengths of the following carboxylic acids is:
$(i)$ $CH_3-CH_2-COOH$
$(ii)$ $CH_3-COOH$
$(iii)$ $C_6H_5-COOH$
$(iv)$ $C_6H_5-CH_2-COOH$

Carboxylic acids have higher boiling points than aldehydes,ketones,and even alcohols of comparable molecular mass. This is due to their:

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