What is the main reason for the fact that carboxylic acids can undergo ionization?

  • A
    Absence of $\alpha-hydrogen$
  • B
    Resonance stabilisation of the carboxylate ion
  • C
    High reactivity of $\alpha-hydrogen$
  • D
    Hydrogen bonding

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$HCOOH$ shows all tests of aldehyde because

In the given reaction :
$CH_3-COOH$ $\mathop{\xrightarrow{(i) Br_2/P}}_{(ii) NaCN, (iii) H_2O/H^{+}/\Delta}$ $[X]$
$[X]$ will be :

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Product $(A)$ of the above reaction is

Among the following acids,the strongest acid is

The increasing order of acidic strength among the following compounds is
$I.$ Benzoic acid
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$III.$ $3, 4-$dinitrobenzoic acid
$IV.$ $4-$methoxybenzoic acid

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