The structure and name of intermediate compound is -

1.  



Cumene hydroperoxide
2.



Cumene hydroperoxide
3.



Cumene hydroperoxide
4. None of these

Subtopic:  Phenols: Preparation & Properties |
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  The IUPAC name of the following compound is:
        
1. Cyclopent-1-en-3-ol
2. Cyclopent-3-en-1-ol
3. Cyclopent-2-en-1-ol
4. Cyclopent-1-en-2-ol

Subtopic:  Alcohols: Preparation & Properties |
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"A" in the reaction below is:

1. Chlorobenzene 2. 1,2-Dichlorobenzene
3. 1,3-dichlorobenzene 4. None of these
Subtopic:  Phenols: Preparation & Properties |
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The IUPAC name of above mentioned compound is:
1. 1-Chloro-3-ethylbutan-3-ol
2. 1-Chloro-3-ethylbutan-1-ol
3. 3-Chloro-3-ethylbutan-1-ol
4. 3-(Chloromethyl)pentan-1-ol

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 reaction of 3-methylbutan-2-ol with HBr gives:

1. 2-Bromo-3-methyl butane 2. 2-Bromo-2-methyl butane
3. 3-Bromo-2-methyl butane 4. 3-Bromo-3-methyl butane
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The reaction of hydrogen iodide with methoxybenzene gives:

1. Phenol 2. Iodomethane
3. Phenol and Iodomethane 4. None of the above
Subtopic:  Ethers: Preparation & Properties, Uses |
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What is the product of the reaction of hydrogen iodide with benzyl ethyl ether?

1. Ethanol

2. Benzyl iodide

3. Benzyl iodide and Ethanol

4. None of the above

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The correct sequence of reactions is:

1.  
2.   
3.
4.

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The correct set of reactions among the following is:

1.
2.
3.
4. None of the above
Subtopic:  Alcohols: Preparation & Properties |
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