Home
Class 12
CHEMISTRY
o-nitrophenol is...

o-nitrophenol is

A

more volatile than p-nitrophenol

B

less volatile than p-nitrophenol

C

Equally volatile as p-nitrophenol

D

Non-volatile

Text Solution

AI Generated Solution

The correct Answer is:
To determine the volatility of ortho-nitrophenol compared to para-nitrophenol, we need to analyze the molecular structures and the type of hydrogen bonding present in each compound. ### Step-by-Step Solution: 1. **Identify the Structures**: - **Ortho-nitrophenol**: The structure consists of a hydroxyl group (-OH) and a nitro group (-NO2) attached to the benzene ring at adjacent positions (ortho position). - **Para-nitrophenol**: The structure consists of a hydroxyl group (-OH) and a nitro group (-NO2) attached to the benzene ring at opposite positions (para position). 2. **Analyze Hydrogen Bonding**: - **Ortho-nitrophenol**: In this compound, the -OH group can form an intramolecular hydrogen bond with the nitro group. This means that the hydrogen bonding occurs within the same molecule, which stabilizes the molecule but does not lead to strong intermolecular interactions. - **Para-nitrophenol**: In this compound, the -OH group can form intermolecular hydrogen bonds with other para-nitrophenol molecules. This leads to stronger interactions between different molecules. 3. **Determine the Effect on Boiling Point**: - **Boiling Point and Volatility Relationship**: The boiling point of a substance is inversely related to its volatility. A higher boiling point indicates lower volatility. - **Ortho-nitrophenol** has intramolecular hydrogen bonding, which does not significantly increase its boiling point. - **Para-nitrophenol** has intermolecular hydrogen bonding, which increases its boiling point due to stronger molecular association. 4. **Conclusion**: - Since ortho-nitrophenol has a lower boiling point due to the lack of significant intermolecular hydrogen bonding, it is more volatile than para-nitrophenol. ### Final Answer: Ortho-nitrophenol is **more volatile than para-nitrophenol**. ---
Doubtnut Promotions Banner Mobile Dark
|

Similar Questions

Explore conceptually related problems

The boiling point of p- nitrophenol is higher than that of o- nitrophenol because.

Explain why p-nitrophenol is more acidic than phenol ?

Knowledge Check

  • Assertion : Boiling point of p-nitrophenol is greater than that of o-nitrophenol. Reason : There is intramolecular hydrogen bonding in p-nitrophenol and intermolecular hydrogen bonding in o-nitrophenol.

    A
    If both assertion and reason are true and reason is the correct explanation of assertion.
    B
    If both assertion and reason are true but reason in not the correct explanation of assertion.
    C
    If assertion is true but reason is false.
    D
    If both assertion and reason are false.
  • P-nitrophenol is a stronger acid than phenol while p-cresol is a weaker acid. Discuss.

    A
    `-CH_(3)` group decreases the electron density on oxygen of O-H group making p-cresol a weaker acid
    B
    `-NO_(2)` group decreases electron density on oxygen of `O - H` group making p-nitrophenol a stronger acid
    C
    `-CH_(3)` group increases the electron density on oxygen of `O -H` group making release of `H^(+)` easier
    D
    `-NO_(2)` group increases the electron density on oxygen of `O - H` group making release of `H^(+)` easier .
  • The most suitable method of separation of 1:1 mixture of ortho and para-nitrophenols is : sublimation chromatography crystallisation steam distillation

    A
    sublimation
    B
    chromatography
    C
    crystallisation
    D
    steam distillation
  • Similar Questions

    Explore conceptually related problems

    Assertion (A) p-nitrophenol is more acidic than phenol. Reason (R) Nitro group helps in the stabilisation of the phenoxide ion by dispersal of negative charge due to resonance.

    Which of the following isomers is move volatile : o-nitrophenol or p-nitrophenol

    Which of the following isomers is more volatile : o-nitrophenol or p-nitrophenol ?

    Assertion: o-nitrophenol has higher boilling point than p-nitrophenol. Reason: Intermolecular hydrogen bonding is present in p-nitrophenol and intrmolecular hydrogen bonding in o-nitrophenol.

    Explain why : o-nitrophenol possesses low boiling point in spite of the presence of hydrogen bonding in it.