The following reaction is the best method to introduce F to benzene:

The structure of intermediate compound A is:

1.		2.
3.		4.

 

The structure of the main product of the following reaction will be:
  \(\xrightarrow[]{Br_2,\ \text{heat or light}}\ \text{Product}\)

1.		2.
3.		4.

Which amine gives the carbylamine test?

1.		2.
3.		4.

When   is reduced with Sn / HCl, the pair of products formed is :

1. Ethanol, hydroxylamine hydrochloride 
2. Ethanol, ammonium hydroxide
3. Ethanol, NH₂OH
4. \(C_3H_5NH_2, H_2O\)

Whose melting point is the highest?

The reagent that is used to change nitromethane into methylhydroxylamine is: 

1. $Zn/NaOH$

2. $Sn/HCl$

3. $Zn/N{H}_{4}Cl$

4. $Zn/HCl$

Which of the following amines doesn't give the carbylamine reaction?

Which of the following is most reactive to electrophilic substitution?

Select the correct option based on statements below:

Assertion (A):	is more basic than
Reason (R):	Delocalization of a lone pair of electrons decreases the basic strength.

Select the correct option based on statements below: