The product 'D' in the below-mentioned reaction will be:

 

1.		2.
3.		4.

 

The example of a nucleophilic substitution reaction among the following is:

1.
2.
3.
4.

The compound that is most susceptible to a nucleophilic attack in the carbonyl group is:

1. ${\mathrm{CH}}_3{\mathrm{COOCH}}_3$

2. ${\mathrm{CH}}_3{\mathrm{CONH}}_2$

3. ${\mathrm{CH}}_3{\mathrm{COOCOCH}}_3$

4. ${\mathrm{CH}}_3\mathrm{COCl}$

In a basic medium, acetophenone yields a stable compound A with C₂H₅ONa.

The structure of A is:

1.		2.
3.		4.

Reduction of aldehydes and ketones into hydrocarbons using amalgam and conc. HCl is called:

1. Clemmensen reduction

2. Cope reduction

3. Dow reduction

4. Wolff-Kishner reduction

A compound with the molecular formula C₅H₁₀ that yields acetone on ozonolysis is:
1. 2-Methyl-2-butene
2. 2-Methyl-1-butene
3. Cyclopentane
4. 3-Methyl-1-butene

The compound on hydrolysis of 50% aqueous sodium hydroxide that produces the corresponding alcohol and acid is:

1. $C_6{H}_{5}C{H}_{2}CHO$

2. $C_6{H}_{5}CHO$

3. $C{H}_{3}C{H}_{2}C{H}_{2}CHO$

4. ${\mathrm{CH}}_3-\stackrel{\mathrm{O}}{\stackrel{\left|\right|}{\mathrm{C}}}-{\mathrm{CH}}_3$

Consider the following compounds:

(i)	C6H5COCl	(ii)
(iii)		(iv)

What is the correct decreasing order of their reactivity towards hydrolysis?

1. (ii) > (iv) > (iii) > (i)

2. (i) > (ii) > (iii) > (iv)

3. (iv) > (ii) > (i) > (iii)

4. (ii) > (iv) > (i) > (iii)