Assertion :Phenol is more reactive than benzene towards $O H$
$B e c a u s e$ Reason: In the case of phenol, the intermediate carbocation is more resonance stabilized.

Both Assertion and Reason are correct and Reason is the correct explanation for Assertion

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Both Assertion and Reason are correct but Reason is not the correct explanation for Assertion

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Assertion is correct but Reason is incorrect

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Assertion is incorrect but Reason is correct

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Solution

The correct option is A Both Assertion and Reason are correct and Reason is the correct explanation for Assertion
Phenol is more reactive than benzene towards
The -OH group attached to benzene in phenol is a highly activating group. The lone pair on oxygen is delocalised into the benzene ring and makes benzene very electron rich

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Q. Read the assertion and reason carefully to mark the correct option out of the options given below:
(a)If both assertion and reason are true and the reason is the correct explanation of the assertion.
(b)If both assertion and reason are true but reason is not the correct explanation of the assertion.
(c)If assertion is true but reason is false.
(d)If assertion is false but reason is true.

Assertion: Phenol is more reactive than benzene towards electrophilic substitution reaction.
Reason : In the case of phenol, the intermediate phenoxide is more resonance stabilized.

Assertion (A) Phenols give o-and p-nitrophenol on nitration with conc. $H N O_{3} a n d H_{2} S O_{4}$ 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.
(e) Both assertion and reason are correct statements but reason is not correct explanation of assertion.

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.
(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.
(e) Both assertion and reason are correct statements but reason is not correct explanation of assertion.

Assertion (A) Phenol forms 2, 4, 6-tribromophenol on treatment with $B r_{2}$ in carbon disulphide at 273K.
Reason (R) Bromine polarises in carbon disulphide.
(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.
(e) Both assertion and reason are correct statements but reason is not correct explanation of assertion.

Assertion (A) Like bromination of benzene, bromination of phenol is also carried out in the presence of Lewis acid.
Reason (R) Lewis acid polarises the bromine molecule.
(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.
(e) Both assertion and reason are correct statements but reason is not correct explanation of assertion.

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Assertion :Phenol is more reactive than benzene towards OHBecause Reason: In the case of phenol, the intermediate carbocation is more resonance stabilized.

Assertion :Phenol is more reactive than benzene towards $O H$
$B e c a u s e$ Reason: In the case of phenol, the intermediate carbocation is more resonance stabilized.