1 |
Cyanogen chloride reacts with ethyl magnesium bromide to give |
CH<sub>3</sub>CH<sub>2</sub>Cl
CH<sub>3</sub>CH<sub>2</sub>Br
C<sub>4</sub>H<sub>10</sub><sup>+</sup>
CH<sub>3</sub>CH<sub>2</sub>CN
|
2 |
For ----------------- Mechanism, the first step involved is the same |
E1 and E2
E2 and S<sub>N</sub>2
S<sub>N</sub>1 and S<sub>N</sub>2
E1 and S<sub>N</sub>1
|
3 |
SN 2 mechanism involves |
1st order kinetics
2nd order kinetics
3rd kinetics
zero order kinetics
|
4 |
Elimination Bimolecular reactions involve |
Second order kinetics
First order kinetics
Third order kinetics
Zero order kinetics
|
5 |
------------------- is not a nucleophile |
H<sub>2</sub>O
NO<sub>3</sub>
BF<sub>3</sub>
NH<sub>3</sub>
|
6 |
SN2 reactions can be carried out with |
Primary alkylhalide
Secondary alkyhalide
Tertiary alkylhalide
All of these
|
7 |
The most reactive Alkyl halide is |
Alkyl Iodide
Alkyl Bromide
Alkyl fluoride
Alkyl Chloride
|
8 |
In primary alkyl halides, the halogen atom is attached to a carbon which is further attached to how many carbon atoms |
Two
Three
One
Four
|
9 |
Which compound is the most reactive one |
benzene
ethene
ethane
ethyne
|
10 |
During nitration of benzene, the active nitrating agent is |
NO<sub>3</sub>
NO<sub>2</sub><sup>+</sup>
NO<sub>2</sub><sup>-</sup>
HNO<sub>3</sub>
|
11 |
Amongst the following, the compound that can be most readily sulphonated is |
toluene
benzene
nitrobenzene
chlorobenzene
|
12 |
Which one is not a meta directing group |
-COOH
-CHO
-COR
-NH<sub>2</sub>
|
13 |
Amongst the following, the compound of that can be most readily sulphonated is |
Toluene
Benzene
Nitro-benzene
Chloro-benzene
|
14 |
m-choronitro benzene is prepared by |
Nitration of chlorobenzene
Nitration of Benzene
Chlorination of Nitrobenzene
Nitration of m-chlorobenzene
|
15 |
The electrophile in Aromatic sulphonation is |
H<sub>2</sub>SO<sub>4</sub>
HSO<sub>4</sub><sup>1-</sup>
SO<sub>3</sub>
SO<sub>3</sub><sup>1+</sup>
|
16 |
Which catalyst is used Friedel Crafts reactions |
AlCl<sub>3</sub>
BeCl<sub>2</sub>
NaCl
HNO<sub>3</sub>
|
17 |
Benzene cannot undergo |
Substitution reactions
addition reactions
oxidation reactions
elimination reactions
|