$\stackrel{{\mathrm{PCl}}_5}{\to }$(A) $\stackrel{{\mathrm{LiAlH}}_4}{\to }$(B) $\stackrel{\mathrm{PCC}}{\to }$(C) $\underset{∆}{\overset{{\mathrm{HO}}^{-}}{\to }}$(D)

(a) 
  (b)  
(c)  
(d) 

Which of the following compounds will undergo decarboxylation on heating?

1. 2 and 3           

2. 3 and 4                 

3. 3 only                   

4. 1 and 4

$\underset{\mathrm{dry} \mathrm{HCl} \mathrm{gas} (\mathrm{major} \mathrm{product});}{\overset{3\mathrm{eq}. \mathrm{EtOH}}{\to }}$ (A); Product A is :

(a)                      (b) 

(c)                       (d) 

Identify the compound C in the following sequence :

$({\mathrm{CH}}_3{)}_2{\mathrm{CHCH}}_2\mathrm{C}\equiv \mathrm{N}\stackrel{\mathrm{HCl}, {\mathrm{H}}_2\mathrm{O}}{\to }$compound A $\underset{2. {\mathrm{H}}_2\mathrm{O}}{\overset{1. {\mathrm{LiAlH}}_4}{\to }}$compound B $\underset{{\mathrm{CH}}_2{\mathrm{Cl}}_2}{\overset{\mathrm{PCC}}{\to }}$compound C 

(a)  $O$
$\left|\right|$
${\left(C{H}_3\right)}_{2}CHCC{H}_3$

                                 
(b) $O$
$\left|\right|$
${\left(C{H}_3\right)}_{2}CHC{H}_{2}COH$

(c) $O$
$\left|\right|$
${\left(C{H}_3\right)}_{2}CHC{H}_{2}CH$                 

(d) $O$
$\left|\right|$
${\left(C{H}_3\right)}_{2}CHC C{H}_{2}OH$

What is compound Z?

${\mathrm{CH}}_3{\mathrm{CH}}_2{\mathrm{CH}}_2\mathrm{Br}\stackrel{\mathrm{NaCN}}{\to }$$\mathrm{X}\underset{\mathrm{heat}}{\overset{{\mathrm{H}}_3{\mathrm{O}}^{+}}{\to }}$$\mathrm{Y}\underset{{\mathrm{H}}^{+}}{\overset{{\mathrm{CH}}_3{\mathrm{CH}}_2\mathrm{OH}}{\to }}$Z

(a) $O$
$\left|\right|$
$C{H}_{3}CH-CHCOH$           

(b) ${\mathrm{CH}}_3{\mathrm{CH}}_2{\mathrm{CH}}_2\mathrm{CH}={\mathrm{NOCH}}_2{\mathrm{CH}}_3$

(c) ${\mathrm{CH}}_3{\mathrm{CH}}_2{\mathrm{CH}}_2\mathrm{CH}({\mathrm{OCH}}_2{\mathrm{CH}}_3{)}_2$         

(d)  $O$
$\left|\right|$
$C{H}_{3}C{H}_{2}COC{H}_{2}C{H}_3$

Identify (A).

(a)      (b)     (c)      (d) 

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

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)