The decreasing order of acidic strength for the following acids is:
$(A)$ $CH_3COOH$
$(B)$ $CH_3CHClCH_2COOH$
$(C)$ $ClCH_2COOH$
$(D)$ $Cl_2CHCOOH$

  • A
    $B > C > A > D$
  • B
    $D > C > B > A$
  • C
    $D > B > C > A$
  • D
    $C > D > B > A$

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Similar Questions

Given below are two statements :
Statement $I :$ The esterification of carboxylic acid with an alcohol is a nucleophilic acyl substitution.
Statement $II :$ Electron withdrawing groups in the carboxylic acid will increase the rate of esterification reaction.
Choose the most appropriate option

Which one is the strongest acid?

Which of the following compounds reacts with methyl magnesium iodide to produce ethyl acetate?

Identify $A$ and $B$ in the following reaction:
$CH_3-CH_3 \stackrel{B}{\longleftarrow} CH_3COOH \stackrel{A}{\longrightarrow} CH_3CH_2OH$
$A \quad B$

Which of the following carboxylic acids will undergo decarboxylation most easily?

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