The IUPAC name of the above compound is:
 

1. 1-Phenylpropan-2-ol
2. 2-Phenylpropan-2-ol
3. 1-Phenylpropan-1-ol
4. 2-Phenylpropan-1-ol

Subtopic:  Alcohols: Preparation & Properties |
 84%
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The IUPAC name of the below compound is:

1.  3,4-Dimethylhexane –1,3,5-triol 

2.  3,5-Dimethylhexane –1,1,5-triol 

3.  3,5-Dimethylhexane –1,3,5-triol 

4.  3,1-Dimethylhexane –1,3,5-triol 

Subtopic:  Alcohols: Preparation & Properties |
 78%
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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 |
 88%
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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
Subtopic:  Alcohols: Preparation & Properties |
 56%
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The reaction of hydrogen iodide with benzyl ethyl ether gives -

1. Ethanol

2. Benzyl iodide

3. Benzyl iodide and Ethanol

4. None of the above

Subtopic:  Ethers: Preparation & Properties, Uses |
 56%
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The correct sequence of reactions is-

1.  
2.   
3.
4.

Subtopic:  Phenols: Preparation & Properties |
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The major product of Williamson’s ether synthesis reaction would be:


1. Benzene
2. Methoxy benzene
3. Ethoxy benzene
4. Ethane

Subtopic:  Ethers: Preparation & Properties, Uses |
 91%
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In the following Williamson’s synthesis reaction,

CH3CH2ONa + CH3-Br → ?

The product will be:

1. 1-Methoxyethane 2. 2-Methoxyethane
3. 3-Methoxyethane 4. 4-Methoxyethane
Subtopic:  Ethers: Preparation & Properties, Uses |
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Match the following:

List I List II
i.  O2N-C6H5-OCH(p) a. 4-Ethoxy-1,1-dimethylcyclohexane
ii.  C2H5OCH2-CH(CH3)2 b. 1-Chloro-2-methoxyethane
iii.  CH3OCH2CH2Cl c. 1-Ethoxy-2-methylpropane
iv.   d. 1-Methoxy-4-nitrobenzene
 
i ii iii iv
1. d c b a
2. c d b a
3. a c b d
4. b c d a
Subtopic:  Ethers: Preparation & Properties, Uses |
 90%
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