The acidic strength of these compounds can be determined based on the substituents attached to the aromatic ring, which influence the electron density and hence the acidity.
- Compound A: Has two \( NO_2 \) groups, which are electron-withdrawing groups that increase the acidity.
- Compound B: Has a \( SO_3H \) group, which is an extremely strong electron-withdrawing group, significantly increasing the acidity, but still lower than the combination of two \( NO_2 \) groups in A.
- Compound C: Has an \( OCH_3 \) group, which is electron-donating and thus lowers the acidity.
- Compound D: Has a \( CH_3 \) group, another electron-donating group, further reducing the acidity.
Thus, the correct order of acidity is \( A > C > D > B \), where compound A is the most acidic, followed by C, D, and B.