The correct acidity order of the following is

Question

The correct acidity order of the following is <img class="img-fluid question-image" alt="image" src="https://cdn.tardigrade.in/img/question/chemistry/1c2647c85463f563b8720b17268102a1-.png" /> (A) (III) > (IV) > (II) > (I) (B) (IV) > (III) > (I) > (II) (C) (III) > (II) > (I) > (IV) (D) (ii) > (III) > (IV) > (I)

Tardigrade Admin · Accepted Answer

Carboxylic acid is stronger acid than phenol. The presence of electron withdrawing group (e.g. Cl) increases acidic strength, while presence of electron donating group (e.g. CH3) decreases acidic strength.

Q. The correct acidity order of the following is

(III) > (IV) > (II) > (I)

(IV) > (III) > (I) > (II)

(III) > (II) > (I) > (IV)

(ii) > (III) > (IV) > (I)

Carboxylic acid is stronger acid than phenol. The presence of electron withdrawing group (e.g. $Cl$ ) increases acidic strength, while presence of electron donating group (e.g. $C H_{3}$ ) decreases acidic strength.

Q. The correct acidity order of the following is

(III) > (IV) > (II) > (I)

(IV) > (III) > (I) > (II)

(III) > (II) > (I) > (IV)

(ii) > (III) > (IV) > (I)

Carboxylic acid is stronger acid than phenol. The presence of electron withdrawing group (e.g. Cl) increases acidic strength, while presence of electron donating group (e.g. CH3​) decreases acidic strength.

Carboxylic acid is stronger acid than phenol. The presence of electron withdrawing group (e.g. $Cl$ ) increases acidic strength, while presence of electron donating group (e.g. $C H_{3}$ ) decreases acidic strength.