What would be the product formed when 1-bromo-3-chlorocyclobutane reacts with two equivalents of metallic sodium in ether?

1.   

2. 

3.    

4. 

X $\stackrel{{\mathrm{Cl}}_2}{\to }$ Benzotrichloride $\stackrel{\mathrm{Hydrolysis}}{\to }$ Y

X and Y respectievely are:

1. benzene, benzaldehyde

2. toluene, benzaldehyde

3. toluene, benzoic acid

4. benzene, benzoic acid

Benzene on reaction with a mixture of HNO₃ and H₂SO₄ followed by reaction of Cl₂/FeCl₃ gives:

1. 3-chloro -1 -nitrobenzene

2. 2-chloro -1 -nitrobenzene

3. 4-chloro -1 -nitrobenzene

4. a mixture of 2-chloro and 4-chloro -1 -nitrobenzene

A yellow precipitate is obtained when aqueous ${\mathrm{AgNO}}_3$ is added to a solution of the compound:

1. ${\mathrm{CCl}}_3\mathrm{CHO}$

2. ${\mathrm{CHI}}_3$

3. ${\mathrm{CHCl}}_3$ 

4. ${\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{CH}}_2\mathrm{Cl}$

In the following sequences of reactions;

${\mathrm{CH}}_3{\mathrm{CH}}_2{\mathrm{CH}}_2\mathrm{I}\stackrel{\mathrm{KOH}(\mathrm{alc}.)}{\to }$(A)$\stackrel{{\mathrm{Br}}_2}{\to }$(B)$\stackrel{{\mathrm{NaNH}}_2/{\mathrm{NH}}_3}{\to }$(C)

the end product (C) is:

1. alkene                                 

2. alkanol

3. alkyne                                   

4. alkyl amine

What is the product of hydrogenation of benzoyl chloride with Pd on BaSO₄?

 1. Benzyl alcohol                       
 2. Benzaldehyde
 3. Benzoic acid                           
 4. Phenol 

Friedel-Craft's reaction of bromobenzene with methyl iodide gives:

1. o-bromotoluene                     

2. p-bromotoluene

3. o-and p-bromotoluenes             

4. m-bromotoluene

Benzyl chloride (C₆H₅CH₂Cl) can be prepared from toluene by chlorination with:

1. SO₂Cl₂

2. SOCl

3. S₂Cl₂

4. NaOCl₂

When vinyl chloride is passed through alcoholic KOH solution:

1. it dissolves                                 

2. it forms vinyl alcohol

3. it forms acetylene                     

4. it has no action

In the following reaction sequence, what is the final product, compound 'Z'?

1.	mixture of
2.
3.
4.