Home
Class 12
CHEMISTRY
Assertion: o-nitrophenol has higher boil...

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.

A

If both A and R are true and R is the correct explanation of A.

B

If both A and R are true but R is not the correct explanation of A.

C

If A is true but R is false

D

If A is false but R is true.

Text Solution

AI Generated Solution

The correct Answer is:
To solve the given question, we need to analyze the assertion and reason provided, and then determine their validity. ### Step 1: Understand the Structures - **Ortho-nitrophenol (o-nitrophenol)** has the nitro group (-NO2) and hydroxyl group (-OH) positioned on adjacent carbon atoms of the benzene ring. - **Para-nitrophenol (p-nitrophenol)** has the nitro group and hydroxyl group positioned on opposite sides of the benzene ring. ### Step 2: Analyze Hydrogen Bonding - **Ortho-nitrophenol** can form **intramolecular hydrogen bonding**. This means that the -OH group can form a hydrogen bond with the -NO2 group within the same molecule, which stabilizes the structure but does not contribute significantly to boiling point. - **Para-nitrophenol** can form **intermolecular hydrogen bonding**. This means that the -OH group of one molecule can form hydrogen bonds with the -NO2 group of another molecule, leading to stronger interactions between molecules. ### Step 3: Compare Boiling Points - Intermolecular hydrogen bonding is generally stronger than intramolecular hydrogen bonding. Therefore, para-nitrophenol, which exhibits intermolecular hydrogen bonding, will have a higher boiling point compared to ortho-nitrophenol, which primarily exhibits intramolecular hydrogen bonding. ### Step 4: Evaluate the Assertion and Reason - **Assertion**: "o-nitrophenol has a higher boiling point than p-nitrophenol." This is **false** because para-nitrophenol has a higher boiling point due to stronger intermolecular hydrogen bonding. - **Reason**: "Intermolecular hydrogen bonding is present in p-nitrophenol and intramolecular hydrogen bonding in o-nitrophenol." This is **true**. ### Conclusion - The assertion is false, and the reason is true. Therefore, the correct answer is that the assertion is incorrect, but the reason is correct. ### Final Answer - The assertion is false, and the reason is true.

To solve the given question, we need to analyze the assertion and reason provided, and then determine their validity. ### Step 1: Understand the Structures - **Ortho-nitrophenol (o-nitrophenol)** has the nitro group (-NO2) and hydroxyl group (-OH) positioned on adjacent carbon atoms of the benzene ring. - **Para-nitrophenol (p-nitrophenol)** has the nitro group and hydroxyl group positioned on opposite sides of the benzene ring. ### Step 2: Analyze Hydrogen Bonding - **Ortho-nitrophenol** can form **intramolecular hydrogen bonding**. This means that the -OH group can form a hydrogen bond with the -NO2 group within the same molecule, which stabilizes the structure but does not contribute significantly to boiling point. ...
Promotional Banner

Similar Questions

Explore conceptually related problems

o-nitrophenol is

Intermolecular hydrogen bonds are not present in ?

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.

P–O–P bond is absent in :-

o-nitrophenol is more volatile than p-nitrophenol it is due to

Assertion : beta- pleated sheet structure of protein shows maximum extension. Reason : Intermolecular hydrogen bonding is present in them.

Show hydrogen bonding in the molecules of o-nitrophenol and p-nitrophenol.

Ortho -nitrophenol is less soluble in water than p -and m- nitrophenols because

Ortho -nitrophenol is less soluble in water than p -and m- nitrophenols because