Which of the following compounds is/are aromatic alcohol?

1. (A), (B), (C), (D)     2. (A), (D)  
3. (B), (C)  4. (A) Only

Subtopic:  Alcohols: Preparation & Properties |
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The proposed mechanism for hydration of ethene to yield ethanol is as follows:

The wrong step in the above mechanism is:

1. Step 1 2. Step 2
3. Step 3 4. Both steps 2 and 3
Subtopic:  Mechanism of Dehydration, Methanol & Ethanol |
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The IUPAC name of the product of  o-hydroxy benzyl alcohol and PClamong the following is :

1. o-Hydroxy benzyl chloride
2. o-Chloromethylphenol
3. o-Chloromethylchlorobenzene
4. p-Hydroxymethylphenol

Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
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The major product (P) of the following reaction is:

1. 2.
3. 4.

Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
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What is the major product formed in the following reaction?
  

1.
2.
3.
4.
Subtopic:  Mechanism of Dehydration, Methanol & Ethanol |
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Select the correct option based on statements below:

Assertion (A): Phenol does not react with NaHCO3 but 2,4,6-trinitrophenol does react with the evolution of CO2
Reason (R): 2,4,6-trinitrophenol is a stronger acid than carbolic acid.
  
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:  Phenols: Preparation & Properties |
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Which of the following represents the correct order of acidity?
 
1. CH3OH >C2H5OH >H2
2. H2O >CH3OH > C2H5OH 
3. CH3OH > H2O >  C2H5OH 
4. C2H5OH > CH3OH >H2
Subtopic:  Alcohols: Preparation & Properties |
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The order of reactivity of the following Compounds in electrophilic monochlorination at the most favourable position is

1.  I < II < IV < III

2.  III < IV < I < II

3.  IV < III < II < I

4.  III < II < IV < I

Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
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1-Phenoxypropane is treated with an excess of conc. Hl at 0°C and the mixture of products is treated with thionyl chloride. The products formed are:

1. n-propanol + Chlorobenzene
2. Phenol + n-propyl iodide
3. n-propyl chloride + Chlorobenzene
4. n-propyl chloride + Phenol

Subtopic:  Ethers: Preparation & Properties, Uses |
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The product of the given reaction is: 
  
1. t-Butylether 
2. 2-Methylpropene 
3. 2-Methylpent-1-ene 
4. 2,2,3,3-Tetramethylbutane 
 
Subtopic:  Phenols: Preparation & Properties |
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