The X and Y in the below mentioned reaction are

	X	Y
1.	Dilute aqueous NaOH, 20 oC	HBr/Acetic acid, 20 oC
2.	Concentrated alcoholic NaOH, 80 oC	HBr/Acetic acid, 20 oC
3.	Diluted aqueous NaOH, 20 oC,	Br2 / CHCl3 , 0 oC
4.	Concentrated alcoholic NaOH, 80 ° C	Br2/CHCl3, 0 oC

Which of the following chloro derivatives of benzene would undergo hydrolysis most readily with aqueous KOH to give the corresponding hydroxy derivative 

Which of the following will have the maximum dipole moment?

1. ${\mathrm{CH}}_3\mathrm{F}$

2. ${\mathrm{CH}}_3\mathrm{Cl}$

3. ${\mathrm{CH}}_3\mathrm{Br}$

4. ${\mathrm{CH}}_3\mathrm{I}$

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

1. 2

2. 4

3. 6

4. 8

The correct order of solvolyis in the following alkyl halide is 

Arrange the following halides in the decreasing order of S_N1 reactivity:

(I) ${\mathrm{CH}}_3{\mathrm{CH}}_2{\mathrm{CH}}_2\mathrm{Cl}$

(II) ${\mathrm{CH}}_2=\mathrm{CHCH}\left(\mathrm{Cl}\right){\mathrm{CH}}_3$

(III) ${\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{CH}\left(\mathrm{Cl}\right){\mathrm{CH}}_3$

1. I > II > III

2. II > I > III

3. II > III > I

4. III > II > I

Replacement of 'Cl' of  chlorobenzene to give phenol requires drastic conditions but chlorine of 2,4- dinitrochloro benzene is readily replaced because

1. ${\mathrm{NO}}_2$ makes the ring electrons rich at ortho and para position

2. ${\mathrm{NO}}_2$ withdraws electrons from meta position

3. ${\mathrm{NO}}_2$ donates electrons at m-position

4. ${\mathrm{NO}}_2$ withdraws electrons from ortho and para positions 

Among the following bromides given below, the order of their reactivity in the S_N1 reaction is 

1. III > II > I

2. II > III > I

3. III > I > II

4. II > I > III

Which haloarenes is most reactive towards electrophilic substitution reaction ?

1.		2.
3.		4.

When chloroform is reacted with excess of NaOH then final product formed is 

1. HCOOH

2. ${\mathrm{CH}}_3\mathrm{COOH}$

3. ${\mathrm{CH}}_3\mathrm{COONa}$

4. HCOONa