Step 1: Effect of substituents on acidity.
Electron-withdrawing groups like \( \text{Cl} \) or \( \text{NO}_2 \) increase the acidity of phenols by stabilizing the negative charge on the oxygen after deprotonation. Conversely, electron-donating groups like \( \text{OCH}_3 \) reduce the acidity of phenol.
Step 2: Conclusion.
Thus, phenol is less acidic than p-methoxyphenol, but more acidic than p-chlorophenol. Therefore, options (A) and (C) are correct.
Final Answer:
\[
\boxed{\text{(A) p-chlorophenol, (C) p-methoxyphenol}}
\]