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a
(III) > (IV) > (II) > (I)
b
(IV) > (III) > (I) > (II)
c
(III) > (II) > (I) > (IV)
d
(II) > (III) > (IV) > (I)
answer is A.
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Detailed Solution
Carboxylic acid is more acidic than phenol. When an electron releasing group is present in the para position to -COOH group in aromatic carboxylic acid, the acidity is reduced. When Cl atom is present in the para position to -OH group in phenol, it increases its acidity because -Cl withdraws electron density from the ring and stabilizes the phenoxide ion.