To determine the correct answer, let's examine both statements separately:
- Statement I: p-nitrophenol is more acidic than m-nitrophenol and o-nitrophenol.
- P-nitrophenol is more acidic due to the electron-withdrawing nitro group, which stabilizes the phenoxide ion through resonance and inductive effects, with the para position maximizing these effects.
- O-nitrophenol's acidity is reduced by steric hindrance and hydrogen bonding. M-nitrophenol benefits less from resonance and inductive effects compared to the para isomer.
- Consequently, p-nitrophenol is indeed more acidic than both m-nitrophenol and o-nitrophenol.
- Statement II: Ethanol will give immediate turbidity with Lucas reagent.
- Lucas reagent (hydrochloric acid and zinc chloride) differentiates alcohols by their reaction rate, indicated by turbidity formation.
- Tertiary alcohols react immediately, secondary alcohols react within minutes, and primary alcohols show no reaction at room temperature.
- Ethanol, a primary alcohol, does not produce immediate turbidity with Lucas reagent.
- Therefore, Statement II is false.
Based on this analysis, Statement I is true because p-nitrophenol's enhanced acidity is accurately explained. Statement II is false as ethanol does not yield immediate turbidity with Lucas reagent.
Therefore, the correct answer is: Statement I is true but Statement II is false.