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 |
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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 |
 87%
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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 |
 89%
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Preparation of ethers by 2 or 3-degree alcohols in an acidic medium is not a suitable method because:

1. In case of secondary or tertiary alcohols, ketone is obtained as a product.
2. In case of secondary or tertiary alcohols, aldehyde is obtained as a product.
3. In case of secondary or tertiary alcohols, alkene is obtained as a product.
4. In case of primary alcohols, alkene is obtained as a product.
Subtopic:  Ethers: Preparation & Properties, Uses |
 72%
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Propanol has a higher boiling point than that of butane because -

1. Butane undergoes intermolecular ionic bonding

2. Propanol undergoes intermolecular H-bonding

3. Propanol undergoes intramolecular hydrogen bonding

4. Butane undergoes intermolecular H-bonding

Subtopic:  Alcohols: Preparation & Properties |
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Identify Z in the following reaction:

\(CH_3CH_2CH=CH_2 \xrightarrow[H_2O,\ H_2O_2,\ OH^-]{B_2H_6} Z \)

1. \(CH_3CH_2CH_2CH_2OH\) 2. \(CH_3CH_2 \ C \ HCH_3 \\~~~~~~~~~~~~~~~~~~| \\~~~~~~~~~~~~~~~~OH\)
3. \(CH_3CH_2CH_2CHO \) 4. \(CH_3CH_2CH_2CH_3 \)
Subtopic:  Alcohols: Preparation & Properties |
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The most acidic compound among the following is:

1.    2.  
3.   4.
Subtopic:  Phenols: Preparation & Properties |
 88%
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Upon dehydration, the below mentioned compound will not give:

1.  2.  
3.    4.  
Subtopic:  Mechanism of Dehydration, Methanol & Ethanol |
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An appropriate set of reactants for the preparation of 1-methoxy-4-nitrobenzene is/are : 
 

1.
2.
3.
4.

Subtopic:  Electrophilic Substitution Reactions, Uses of Phenols |
 78%
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