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A : p - nitrophenol has high pK(a) in c...

A : p - nitrophenol has high `pK_(a)` in comparison to o-nitrophenol
R : In o-nitrophenol , intermolecular H-bonding is present

A

If both Assertion & Reason are true and the reason is the correct explanation of the assertion, then mark (1)

B

If both Assertion & Reason are true but the reason is not the correct explanation of the assertion, then mark (2)

C

If Assertion is true statement but Reason is false , then mark (3)

D

If both Assertion and Reason are false statements , then mark (4)

Text Solution

AI Generated Solution

The correct Answer is:
To analyze the assertion and reason provided in the question, we will break down the concepts of pKa, acidity, and hydrogen bonding in ortho- and para-nitrophenol. ### Step-by-Step Solution: 1. **Understanding pKa and Acidity**: - The pKa value is a measure of the acidity of a compound. A higher pKa value indicates a weaker acid, while a lower pKa value indicates a stronger acid. - Therefore, if para-nitrophenol has a higher pKa value than ortho-nitrophenol, it means that para-nitrophenol is a weaker acid compared to ortho-nitrophenol. 2. **Structure of Ortho- and Para-Nitrophenol**: - Para-nitrophenol has the nitro group (NO2) positioned at the para position relative to the hydroxyl group (OH). - Ortho-nitrophenol has the nitro group positioned at the ortho position relative to the hydroxyl group. 3. **Intermolecular Hydrogen Bonding in Ortho-Nitrophenol**: - In ortho-nitrophenol, the proximity of the hydroxyl group and the nitro group allows for intramolecular hydrogen bonding, which stabilizes the molecule. - This intramolecular hydrogen bonding reduces the availability of the hydrogen atom from the hydroxyl group to dissociate as a proton (H+), thus increasing the acidity of ortho-nitrophenol compared to para-nitrophenol. 4. **Conclusion on Assertion and Reason**: - The assertion (A) that para-nitrophenol has a higher pKa than ortho-nitrophenol is true. - The reason (R) that intermolecular hydrogen bonding is present in ortho-nitrophenol is misleading. It should be noted that it is intramolecular hydrogen bonding that affects the acidity. - Therefore, while both the assertion and reason are true, the reason does not correctly explain the assertion. ### Final Answer: - Assertion (A) is true. - Reason (R) is true but does not explain (A) correctly.
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o-Nitrophenol has lower/higher pk_(a) value than m-nitrophenol.

Boiling point of p-nitrophenol is more than O-nitrophenol why?

Knowledge Check

  • o-nitrophenol is

    A
    more volatile than p-nitrophenol
    B
    less volatile than p-nitrophenol
    C
    Equally volatile as p-nitrophenol
    D
    Non-volatile
  • Assertion (A) : p-Nitrophenol has a higher melting point than o-nitrophenol. Reason (R) : o-Nitrophenol exhibits intermolecular hydrogen bonding.

    A
    Both A and R are true and R is the correct explanation of A.
    B
    Both A and R are true and R is not a correct explanation of A.
    C
    A is true but R is false.
    D
    A is false but R is true.
  • p-nitrophenol and o-nitrophenol are separated by

    A
    Crystallisation
    B
    Fractional crystallisation
    C
    Distillation
    D
    Steam distillation
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