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Arrange in increasing order of acidity

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A. I > II > III
B. III > II > I
C. I > III > II
D. II > I > III

Last updated date: 16th Jun 2024
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Hint: In Chemistry, there are three types of substances namely acidic, basic, and neutral. It all is related to the amount of hydrogen ion that the compound can generate. The acidic substance turns moist litmus paper bred and the basic ones turn the litmus paper blue. The neutral compounds don't affect the litmus paper.

Complete step by step answer:
The inductive effect $(I)$ is the effect regarding the transmission of the inequality in the sharing of the electron during the bonding process through the chain of atoms in the may be the reason for a permanent dipole in the compound due to this effect.
The electron-withdrawing effect is termed negative ($ - I$) and the electron-donating effect is termed the positive inductive effect ($ + I$).
Acidic strength of the compound is increased due to the presence of the groups showing ($ - I$) effect. The $ - OH$ group present is electrons withdrawing through the inductive effect.
The strongest acid must have the most stable conjugate base. That is why for the alcohol, the acidity trend is $1^\circ > 2^\circ > 3^\circ $ . The methyl groups compensate for the electrons withdrawn by the hydroxyl group. The tertiary carbon compensates the highest for the inductive effect hence nullifying it but the primary carbon is not able to do so hence is the most acidic.

So, the correct answer is Option A.

Note: Though the hydroxyl group is electron-withdrawing by inductive effect, it is electron-donating through the resonance effect.
The mesomeric effect is the property that depends on the substituent group that is attached to the main is related to the polarity shift that occurs in the molecule due to the presence of the substituent group on the main compound. The interaction of the pi- bonds with the lone pair of the compound or another pi-bond is the action that results in the mesomeric effect.