Monochlorination of toluene in sunlight followed by hydrolysis with aq. NaOH yields:

1.  o-Cresol                                   

2.  m-Cresol

3.  2, 4- Dihydroxytoluene         

4.  Benzyl alcohol

How many alcohols with molecular formula ${\mathrm{C}}_4{\mathrm{H}}_{10}\mathrm{O}$ are chiral in nature?

1. 1               

2. 2             

3. 3             

4. 4

What is the correct order of reactivity of alcohols in the following reaction?
               $\mathrm{R}-\mathrm{OH}+\mathrm{HCl} \stackrel{{\mathrm{ZnCl}}_2}{\to }\mathrm{R}-\mathrm{Cl} +{\mathrm{H}}_2\mathrm{O}$

1. 1° > 2°> 3°                                 

2. 1° < 2°> 3°

3. 3°> 2°> 1°                                   

4. 3°> 1°> 2°

${\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{OH}$ can be converted into${\mathrm{CH}}_3\mathrm{CHO}$ by:
1. Catalytic hydrogenation
2. Treatment with LiAI${\mathrm{H}}_4$
3. Treatment with pyridinium chlorochromate
4. Treatment with KMn${\mathrm{O}}_4$

The process of converting alkyl halides into alcohols involves .........

1. Addition reaction                           

2.  Substitution reaction

3. Dehydrohalogenation reaction   

4.  Rearrangement reaction

Which of the following compounds is aromatic alcohol?

The correct IUPAC name of the given compound is:

1.  2-Chloro-5-hydroxyhexane             
2.  2-Hydroxy-5-chlorohexane
3.  5-Chlorohexan-2-ol                           
4.  2-Chlorohexan-5-ol

Which of the following species can act as the strongest base?

1.	\(^\ominus \mathrm{OH}\)
2.	\(^\ominus \mathrm{O R}\)
3.	\({ }^{\ominus} \mathrm{OC}_6 \mathrm{H}_5\)
4.

Arrange the following compounds in increasing order of boiling point.

Propan-1-ol, butan-1-ol, butan-2-ol, pentan-1-ol

1.  Propan-1-ol, butan-2-ol, butan-1-ol, pentan-1-ol

2.  Propan-1-ol, butan-1-ol, pentan-1-ol ,butan-2-ol

3.  Butan-2-ol,propan-1-ol, butan-1-ol, pentan-1-ol

4.  Propan-1-ol, butan-1-ol, butan-2-ol, pentan-1-ol

Reagents used to convert RCHO into  RCH₂OH among the following are:

(a) H₂ /Pd or Pt

(b) LiAIH₄

(c) NaBH₄

(d) Reaction with RMgx followed by hydrolysis

1. (a, b, c)
2. (b, c, d)
3. (a, c, d)
4. (a, b, d)