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The major product of the following reaction sequence will be

(1)PhCOCl/Pyridine(2)CH3COCl/AlCl3
(3)Zn-Hg/HCl/(4)Br2/Fe

1. 
2.
3.
4.
Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
 55%
Level 3: 35%-60%
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Select the correct option based on statements below:

Assertion (A): -OH, -OCH3 groups are o, p-directing.
Reason (R): Ring is activated by the resonance effect of -OH, -OCH3 groups.
  
1. Both (A) and (R) are true and (R) is the correct explanation of (A).
2. Both (A) and (R) are true but (R) is not the correct explanation of (A).
3. (A) is true but (R) is false.
4. Both (A) and (R) are false.
Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
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Level 2: 60%+
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Select the correct option based on statements below:

Assertion (A): Like the bromination of benzene, bromination of phenol is carried out in the presence of Lewis acid.
Reason (R): Lewis acid polarizes the bromine molecule.
 
1. Both (A) and (R) are True and (R) is the correct explanation of (A).
2. Both (A) and (R) are True but (R) is not the correct explanation of (A).
3. (A) is True but (R) is False.
4. (A) is False but (R) is True.
Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
Level 3: 35%-60%
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Select the correct option based on the statements below:

Assertion (A): Phenols give o-and p-nitrophenol on nitration with conc. HNO3 and H2SO4 mixture.
Reason (R): —OH group in phenol is o-, p-directing.
 
1. Both (A) and (R) are True, and (R) is the correct explanation of (A).
2. Both (A) and (R) are True but (R) is not the correct explanation of (A).
3. (A) is True but (R) is False.
4. (A) is False but (R) is True.
Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
Level 3: 35%-60%
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The group that activates the benzene ring towards electrophilic substitution reaction is:

1. OH 2. NO2
3. CN 4. COOH
Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
 79%
Level 2: 60%+
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The alkoxy group in aryl alkyl ethers activates the benzene ring towards:

1. Nucleophilic addition reaction

2. Electrophilic addition reaction

3. Nucleophilic substitution reaction

4. Electrophilic substitution reaction

Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
 63%
Level 2: 60%+
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An appropriate set of reactants for the preparation of 1-methoxy-4-nitrobenzene is/are : 

1.
2.
3. \(\mathrm{CH_3-CH_2-CH_2-O-CH_3+HBr}\)
4. \(\mathrm{(CH_3)_3C-OC_2H_5+HI}\)

Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
 80%
Level 1: 80%+
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In Kolbe’s reaction, 

 

the product formed will be:

1.  para-Salicylaldehyde

2.  ortho-Salicylaldehyde

3. para-Salicylic acid

4. ortho-Salicylic acid

Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
 70%
Level 2: 60%+
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In Reimer-Tiemann reaction

the product will be:

1. ortho-Salicylaldehyde

2. para-Salicylaldehyde

3. meta-Salicylaldehyde

4. All of the above

Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
 86%
Level 1: 80%+
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In the following Williamson ether synthesis reaction, what will be the major product?

      

1. 1-Methoxypropane

2. 2-Methoxypropane

3. 3-Methoxypropane

4. All of the above

Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
 74%
Level 2: 60%+
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