Ortho nitrophenol is more acidic than ortho methoxy phenol because:

1.	The NO2-group increases the electron density in phenol while the methoxy group decreases the electron density in phenol
2.	The nitro-group is an electron-withdrawing group while the methoxy group is an electron-releasing group
3.	The methoxy-group is an electron-withdrawing group while the nitro group is an electron-releasing group
4.	None of the above

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

The IUPAC name of the above compound is:

1. 2, 2, 2-Trimethylpentan-3-ol

2. 2, 2, 4-Trimethylpentan-3-ol

3. 2, 2, 3-Trimethylpentan-3-ol

4. 1, 1, 3-Trimethylpentan-3-ol

The IUPAC name of the above compound is -

1. 2-Methylbutan-1-ol

2. 2-Methylbutan-2-ol

3. 1-Methylbutan-2-ol

4. 1-Methylbutan-1-ol

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 

The IUPAC name of

1. 3,3-Diethylphenol

2. 2,2-Diethylphenol

3. 1,3-Diethylphenol

4. 2,3-Diethylphenol

The IUPAC name of the above compound is:

The IUPAC name of the following compound is:
 

1. 1-Ethoxy-3-methylpentane

2. 3-Ethoxy-1-methylpentane

3. 2-Ethoxy-3-methylpentane

4. 3-Ethoxy-2-methylpentane

The IUPAC name of the following compound is - 

1. Cyclohexane ethanol 

2. Cyclohexane methanol 

3. Cyclohexyl ethanol 

4. Cyclohexyl methanol 

The structure and name of intermediate compound is -

1.	Cumene hydroperoxide
2.	Cumene hydroperoxide
3.	Cumene hydroperoxide
4.	None of these