How is m-Bromotoluene prepared?

1.	Bromination of toluene
2.	Friedel Craft’s reaction of bromobenzene with CH3Cl
3.	Bromination of nitrobenzene and subsequent replacement of –NO2 group with an ethyl group
4.	Bromination of Aceto–p–toluidine followed by hydrolysis and deamination

Which of the following molecules can readily undergo the S_N2 mechanism?

1.	\(\left(\mathrm{CH}_3\right)_3 \mathrm{C}-\mathrm{Cl} \)	2.	\(\mathrm{CH}_2=\mathrm{CH}-\mathrm{Cl} \)
3.	\(\mathrm{CH}_2=\mathrm{CH}-\mathrm{CH}_2-\mathrm{CH}_2 \mathrm{Cl}\)	4.

Sandmeyer's reaction described by among the following is:

1.
2.
3.
4.

Products (A) and (B) in the given below reactions, respectively, are:
 

	(A)	(B)
1.
2.
3.
4.	None of the above

Among the following, which hydrolysis reaction occurs at the slowest rate:

1.
2.
3.
4.

Which of the options is correct about product (A)?

1. Product is aromatic  

2. Product has a high dipole moment

3. Product has less resonance energy          

4. Both A and B

Product A is:

1.		2.
3.		4.

The X and Y in the below mentioned reaction are

What is the total number of chiral products produced by monochlorination of 2-methylbutane ?

1. 2

2. 4

3. 6

4. 8

Which of the following reactions cannot form new carbon-carbon bonds?

1. Reimer-Tiemann reaction

2. Cannizaro reaction

3. Wurtz reaction

4. Friedel-Crafts acylation