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The strongest acid among the following a...

The strongest acid among the following aromatic compound is:

A

o-Nitrophenol

B

p-Chlorophenol

C

p-Nitrophenol

D

m-Nitrophenol

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The correct Answer is:
To determine the strongest acid among the given aromatic compounds, we will analyze the effects of substituents on their acidity. ### Step-by-Step Solution: 1. **Identify the Compounds**: We need to consider the aromatic compounds given in the question. Let's assume we have nitrophenol and chlorophenol as the main candidates. 2. **Understand Electron-Withdrawing Groups**: Both the nitro group (-NO2) and the chlorine atom (-Cl) are electron-withdrawing groups. Electron-withdrawing groups increase the acidity of aromatic compounds by stabilizing the negative charge on the conjugate base formed after deprotonation. 3. **Compare the Effects of Substituents**: - **Nitrophenol**: The nitro group is a strong electron-withdrawing group due to its resonance and inductive effects. It can stabilize the negative charge on the phenoxide ion (the conjugate base) formed when nitrophenol loses a proton. - **Chlorophenol**: The chlorine atom is also an electron-withdrawing group, but it is less effective than the nitro group in stabilizing the negative charge due to its weaker resonance effect. 4. **Consider Resonance Effects**: - In nitrophenol, the nitro group can participate in resonance at the ortho and para positions, which helps stabilize the conjugate base. - In chlorophenol, the chlorine can also participate in resonance, but its effect is weaker than that of the nitro group. 5. **Analyze Ortho and Para Positions**: - **Ortho-Nitrophenol**: While it can stabilize the conjugate base through resonance, it can also form intramolecular hydrogen bonding, which reduces its acidity. - **Para-Nitrophenol**: This compound does not have the intramolecular hydrogen bonding issue and can effectively stabilize the conjugate base through resonance. 6. **Conclusion**: Since para-nitrophenol has the strongest electron-withdrawing effect and does not suffer from the intramolecular hydrogen bonding that affects ortho-nitrophenol, it is the strongest acid among the compounds considered. ### Final Answer: The strongest acid among the given aromatic compounds is **para-nitrophenol**. ---

To determine the strongest acid among the given aromatic compounds, we will analyze the effects of substituents on their acidity. ### Step-by-Step Solution: 1. **Identify the Compounds**: We need to consider the aromatic compounds given in the question. Let's assume we have nitrophenol and chlorophenol as the main candidates. 2. **Understand Electron-Withdrawing Groups**: ...
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