Determine the compound (B) formed as the product of the given reaction.

 

1.		2.
3.		4.

 $\underset{{\mathrm{H}}_3\mathrm{O}+}{\overset{{\mathrm{CH}}_3\mathrm{MgBr}\left(\mathrm{excess}\right)}{\to }}$Product,

Product is:-

1.

2.

3.

4.

$\stackrel{{\mathrm{FeCl}}_3}{\to }$ Product(Major):-

(1)

(2)

(3)

(4)

Which of the following is correctly matched

(a)   + H₂$\stackrel{\mathrm{Pd}-{\mathrm{BaSO}}_4}{\to }$ Rosenmund Reduction

(b) $\to$Curtius Reaction

(c) $\stackrel{\mathrm{KOH}}{\to }$ Hoffmann's bromamide reaction

(d) $\underset{{\mathrm{CH}}_3-\mathrm{Cl}}{\overset{\mathrm{KOH}}{\to }}$ Gabriel pthalimide reaction
 

(a)
(b)
(c)
(d)

1. a, d

2. a, b, d

3. b, c, d

4. All of the above

Which of the following acid is most easily decarboxylate :-

1.

2.

3.

4.

Identify the product (c) in the series

CH₃CN$\stackrel{\mathrm{Na}/{\mathrm{C}}_2{\mathrm{H}}_5\mathrm{OH}}{\to }$A$\stackrel{\mathrm{HNO}2}{\to }$B$\stackrel{{\mathrm{KMnO}}_4,{\mathrm{H}}^{+}}{\to }$C

1. CH₃COOH

2. CH₃CH₂NHOH

3. CH₃CONH₂

4. CH₃CHO

The slowest step of Cannizarro's reaction is

1. Attack of nucleophilic

2. Hydride shift

3. Formation of anion

4. Transfer of proton

Which acid deravative is most reactive towards nucleophilic substitution reaction?

1. CH₃COCl

2. (CH₃CO)₂O

3. CH₃COOC₂H₅

4. CH₃CONH₂