The hydrogenation of benzoyl chloride in the presence of Pd and BaSO₄ gives:

1. Benzyl alcohol

2. Benzaldehyde

3. Benzoic acid

4. Phenol

An alkene “A” on reaction with O₃ and Zn - H₂O gives propanone and ethanal in an equimolar ratio. The addition of HCl to alkene “A” gives “B” as the major product. The structure of product “B” is:

1.		2.
3.		4.

What is product 'B' in the below mentioned reaction?

1.		2.
3.		4.

The formation of cyanohydrin from acetone is an example of:

1. Nucleophilic substitution. 

2. Electrophilic substitution.

3. Electrophilic addition. 

4. Nucleophilic addition.

2-Methyl propene on oxidation with hot KMnO₄ gives:

1. Acetone

2. Ethanoic acid

3. CO₂ and H₂O 

4. Both 1 & 3

What is the most suitable reagent for the below mentioned conversion?

${\mathrm{CH}}_3—\mathrm{CH}=\mathrm{CH}—{\mathrm{CH}}_2—\stackrel{\mathrm{O}}{\mathrm{C}}$
$\left|\right|$ $-{\mathrm{CH}}_3$ $$ $\to$ $$
$$ ${\mathrm{CH}}_3-\mathrm{CH}=\mathrm{CH}—{\mathrm{CH}}_2—\stackrel{\mathrm{O}}{\mathrm{C}}$
$\left|\right|—\mathrm{OH}$

1.  Tollens' reagent 

2.  Benzoyl peroxide

3.  ${\mathrm{I}}_2$ and NaOH solution

4.  Sn and NaOH solution

The conversions can be used for Clemmensen reduction are:

a.  Benzaldehyde into benzyl alcohol.

b.  Cyclohexanone into cyclohexane.

c.  Benzoyl chloride into benzaldehyde.

d.  Benzophenone into diphenyl methane.

Match the common names given in Column I with the IUPAC names given in Column II.

Codes

Match the acids given in Column I with their correct IUPAC names given in Column II and mark the appropriate option:

Codes

The reaction that does not give benzoic acid as the major product is:

1.	\(\xrightarrow{K_2Cr_2O_7}\)	2.	\(\xrightarrow[(ii)H_3O^+]{(i)NaOCl}\)
3.	\(\xrightarrow{PCC}\)	4.	\(\xrightarrow{KMnO_4/H^+}\)