$\underset{\left(\mathrm{i}\right){\mathrm{H}}^{+}}{\overset{\left(\mathrm{i}\right)\mathrm{KBrO},∆}{\to }} \left(\mathrm{X}\right)\stackrel{∆}{\to \left(\mathrm{Y}\right)}$

Hence the product (Y) in the above sequence of reactions, is :

(a)  (b)   (c)   (d) 

The action of bromine water (excess) on salicylic acid results in the formation of:-

(1) 

(2) 

(3) 

(4) 

An organic compound having the molecular formula C₈H₁₀O on being heated with I₂ and dilute NaOH gives a yellow precipitate. The expected compound is:

(a) C₆H₅CH₂CH₂OH

(b) 

(c) 

(d) 

The Birch reduction of benzoic acid gives:-
(a)  
(b)  
(c)  
(d) 

ph-CHO  +   2 $\stackrel{{\mathrm{H}}_2{\mathrm{SO}}_4}{\to }$ major product of this reaction is:

(a) ph₃CH

(b) $OH$
$|$
$Ph-C-Ph$
$|$
$Ph$

(c) 

(d) ph₂CH₂

Which of the following acid gives positive Tollen's reagent test.

(1) $({\mathrm{CH}}_2{)}_2{<}_{{\mathrm{CO}}_2\mathrm{H}}^{{\mathrm{CO}}_2\mathrm{H}}$           

(2) ${\mathrm{CH}}_2{<}_{{\mathrm{CO}}_2\mathrm{H}}^{{\mathrm{CO}}_2\mathrm{H}}$           

(3) $\underset{|}{\mathrm{C}}{\mathrm{O}}_2\mathrm{H}$
${\mathrm{CO}}_2\mathrm{H}$

(4) HCO₂H

Acetaldehyde and benzaldehyde can be differentiated by:

1. Fehling test

2. Iodoform test

3. Tollen's reagent

4. Both (1) and (2)

When vapours of acetic acid are passed over.....at $300°\mathrm{C}$ we get acetone.

1. ${\mathrm{Al}}_2{\mathrm{O}}_3$

2. $\mathrm{CuO}$

3. $\mathrm{MoO}$

4. $\mathrm{Cu}$

Formaldehyde is not used in:

(1) adhesives                 

(2) bakelite

(3) tooth powders           

(4) explosives

Ketones can be prepared by:

(1) Rosenmund's reduction

(2) Stephen's reduction

(3) both (1) and (2)

(4) none of the above