CH₃CH₂Cl$\stackrel{\mathrm{NaCN}}{\to }$X $\stackrel{\mathrm{Ni}/{\mathrm{H}}_2}{\to }$Y$\stackrel{\mathrm{Acetic} \mathrm{anhydride}}{\to }$Z

In the above reaction sequence, Z is

1. CH₃CH₂CH₂NHCOCH₃

2. CH₃CH₂CH₂NH₂

3. CH₃CH₂CH₂CONHCH₃

4. CH₃CH₂CH₂CONHCOCH₃

Oxidation of allylic alcohol, (CH₂=CH-CH₂OH) gives a mixture of oxalic acid and formic acid. If this oxidation is done in presence of bromine. One would expect only:

1. Oxalic acid

2. Formic acid

3. Succinic acid

4. Acrylic acid

Consider the following reaction, 

Ethanol $\stackrel{{\mathrm{PBr}}_3}{\to }$X$\stackrel{\mathrm{Alc}.\mathrm{KOH}}{\to }$Y$\underset{\left(\mathrm{ii}\right){\mathrm{H}}_2\mathrm{O}, \mathrm{heat}}{\overset{\left(\mathrm{i}\right) {\mathrm{H}}_2{\mathrm{SO}}_4, \mathrm{room} \mathrm{temperature}}{\to }}$Z

product Z is:

1. CH₂=CH₂

2. CH₃CH₂OCH₂CH₃

3. CH₃CH₂OSO₃H

4. CH₃CH₂OH

Which of the following are known as mercaptans?

1. Thio-alcohols                         

2. Thio-ethers

3. Thio-aldehydes                     

4. Thio-acids

Glycol condenses with ketones to give:

1. Cyclic acetals                   
2. Cyclic ketals
3. Acetaldehyde                   
4. oxalic acid

Salol is used as:

1. antiseptic                               

2. antipyretic

3. both 1. and 2.                     

4. none of these

Given is a reaction for your reference:

\(CH_3CH_2CH_2OH \xrightarrow[160\ - \ 180 ^\circ C]{Conc.\ H_2SO_4}\ X\ \xrightarrow{Br_2}\ Y\)
\( Y\ \xrightarrow[2.\ NaNH_2]{1.\ Alc.\ KOH}\ Z\)

The final product Z is:

1.		2.
3.		4.	\(CH_3-C\equiv CH\)

Ethyl propanoate on reduction with LiAlH₄ yields:

1. Methanol

2. Ethanol and Propanol

3. Propane

4. Mixture of ethanol and methanol

Phenol does not react with: 

1. Na₂CO₃                                 

2. NaOH

3. NaHCO₃                                 

4. KOH

The most acidic alcohol among the following is -

1. Methanol                               

2. Ethanol

3. Isopropyl alcohol                     

4. t-Butyl alcohol