The correct answer is option (A): I>III>II
The acidity can be determined by the stability of the conjugate base formed after losing a proton. More stable the conjugate more stronger the acid. I: 4-Nitrobenzoic acid: it has a strong electron-withdrawing group. The negative charge on the base is stabilized by the electron-withdrawing effect of the nitro group. II 4-Methoxybenzoic acid: The methoxy group is attached to the beneze ring. The Methoxy group is electron donating but is not as effective as the nitro group. III Benzoic acid: It has no substituent group Therefore, the order of acidity will be I>III>II