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Assertion (A) Phenols give o-and p-nitro...

Assertion (A) Phenols give o-and p-nitrophenol on nitration with conc. `HNO_(3)` and `H_(2)SO_(4)` mixture.
Reason (R) `-OH` group in phenol is o-,p-directing.

A

Assertion and reason both are correct and reason is correct explanation of assertion.

B

Assertion and reason both are wrong statements.

C

Assertion is correct statement but reason is wrong statement.

D

Assertion is wrong statement but reason is correct statement.

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The correct Answer is:
To solve the question, we need to analyze both the assertion and the reason provided. ### Step 1: Analyze the Assertion The assertion states that phenols give o- and p-nitrophenol on nitration with a mixture of concentrated HNO3 and H2SO4. - When phenol is treated with concentrated nitric acid (HNO3) and concentrated sulfuric acid (H2SO4), it undergoes nitration. - The expected products of this reaction are indeed ortho (o-) and para (p-) nitrophenol. However, under strong nitrating conditions (like the mixture of HNO3 and H2SO4), phenol can further react to form 2,4,6-trinitrophenol, commonly known as picric acid. Thus, the assertion that phenol gives only o- and p-nitrophenol is incorrect because the reaction can lead to the formation of a more highly nitrated product. ### Step 2: Analyze the Reason The reason states that the -OH group in phenol is o-, p-directing. - The -OH (hydroxyl) group is indeed an electron-donating group, which activates the aromatic ring for electrophilic substitution. - This means that when electrophiles (like NO2+) approach the aromatic ring, they are more likely to attack the ortho and para positions relative to the -OH group. Thus, the reason is correct as it accurately describes the directing effects of the -OH group. ### Conclusion - The assertion is incorrect because the reaction with concentrated HNO3 and H2SO4 can lead to the formation of 2,4,6-trinitrophenol (picric acid), not just o- and p-nitrophenol. - The reason is correct because the -OH group is indeed o-, p-directing. ### Final Answer - Assertion (A) is incorrect. - Reason (R) is correct. - Therefore, the correct option is D: Assertion is wrong, but the reason is correct. ---

To solve the question, we need to analyze both the assertion and the reason provided. ### Step 1: Analyze the Assertion The assertion states that phenols give o- and p-nitrophenol on nitration with a mixture of concentrated HNO3 and H2SO4. - When phenol is treated with concentrated nitric acid (HNO3) and concentrated sulfuric acid (H2SO4), it undergoes nitration. - The expected products of this reaction are indeed ortho (o-) and para (p-) nitrophenol. However, under strong nitrating conditions (like the mixture of HNO3 and H2SO4), phenol can further react to form 2,4,6-trinitrophenol, commonly known as picric acid. ...
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NCERT EXEMPLAR-ALCOHOLS, PHENOLS AND ETHERS-Alcohols, Phenols And Ethers
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  2. Arrange water, ethanol and phenol in increasing order of acidity and g...

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  3. Match the structures of the compounds given in Column I with the name ...

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  4. Match the starting material given in Column I with the products formed...

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  5. Match the items of Column I with items of Column II.

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  6. Match the items of Column I with items of Column II.

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  7. Assertion (A) Addition reaction of water to but-1-ene in acidic medium...

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  8. Assertion (A) p-nitrophenol is more acidic than phenol. Reason (R) N...

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  9. Assertion (A) IUPAC name of the compound CH(3)-underset(CH(3))unders...

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  10. Assertion (A) Bond angle is ethers is slightly less than tetrahedral a...

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  11. Assertion (A) Boiling points of alcohols and ethers are high. Reason...

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  12. Assertion (A) Like bromination of benzene, bromination of phenol is al...

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  13. Assertion (A) o-nitrophenol is less soluble in water than the m and p-...

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  14. Assertion (A) Ethanol is a weaker acid than phenol. Reason (R) Sodiu...

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  15. Assertion (A) Phenol forms 2, 4, 6-tribromophenol o treatement with Br...

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  16. Assertion (A) Phenols give o-and p-nitrophenol on nitration with conc....

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  17. Write the mechanism of the reaction of HI with methoxybenzene.

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  18. (a) Name the starting material used in the industrial preparation of p...

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  19. How can phenol be converted to aspirin ?

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  20. Explain a process in which a biocatalyst is used industrial preparatio...

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