Step 1: Understanding the Concept:
Acidity depends on the stability of the conjugate base. Phenols are more acidic than alcohols due to resonance stabilization of the phenoxide ion.
Step 2: Detailed Explanation:
Alcohols (like ethanol) are neutral or very weakly acidic (pKa ≈ 16). Phenols are more acidic (pKa ≈ 10).
The presence of electron-withdrawing groups (like -NO2 at p-position) increases the acidity of phenol. Electron-donating groups (like -CH3 at p- or m-position) decrease the acidity of phenol.
However, all phenols are still much stronger acids than ethanol. Therefore, ethanol is the weakest acid among the given options.
Step 3: Final Answer:
Ethanol is the weakest acid.