| 1 |
Grignard's reagent on treatment with chloramine give |
Acetamide
Primary amice
Secondary amice
Urea
|
| 2 |
Hydrolysis of Grignard's reagent yields |
Alcohol
Aldyhyde
Ester
Alkane
|
| 3 |
Alkyle magnesium halides are known as |
Simon-smith reagent
Tollen's reagent
Grignard's reagent
Barford's reagent
|
| 4 |
A reaction in which an atom or a group of atoms replaces an atom or a group of atoms in the molecule of a substance is known as |
Addition reaction
Condensation reaction
Elimination reaction
Substitution reaction
|
| 5 |
Alkyl halides on treatment with aqueous KOH give |
Phenol
Alcohol
Aldehyde
Ketone
|
| 6 |
Action of Zn with alkyl halides in the presence of an inert solvent forms higher alkanes. This reaction is known as |
Wurtz reaction
Frankland's reaction
Cannizaro reaction
Kalobe's reaction
|
| 7 |
Dehydrohalogenation of alkyl halides give |
Alkanes
Alkenes
Alkynes
Alkdehyde
|
| 8 |
By reaction Grignard's reagent with the HCHO we get |
1° - alcohol
2° - alcohol
3° - alcohol
All of these
|
| 9 |
Alkyl halides on treatment with Zn and HCI gives |
Alkanes
Alkenes
Alkynes
Alcohols
|
| 10 |
Alkyl halides on treatment with metallic Na give |
Alkynes
Alkenes
Alkanes
Alcohols
|
| 11 |
The reaction of alcohol with SOCI2in the presence of pyridine as catalyst gives |
Acids
Acid chloride
Alkyl halide
Benzene
|
| 12 |
Halogens on treating with silver salts of acids give |
Alcohol
Ester
Phenol
Alkyl halide
|
| 13 |
E1mechanism is generally shown by |
1° - RX
2° - RX
3° - RX
None of these
|
| 14 |
When alkyl halides are heated with aqueous solution of ammonia at about 100°C, amines are formed. This reaction is known as |
Williamsons synthesis
GHoffmans reaction
Wurtz reaction
Clemensen reaction
|
| 15 |
Alkanes may be prepared by the reaction of alkyl halides with |
Alcohol
Carboxylic acid
Grignard reagents
None of these
|
| 16 |
Reduction of alkyl halides give |
Alkanes
Alkenes
Ketones
Ether
|
| 17 |
Alkyle halides can be prepared by treating halogen acids with |
Ethane
Ethanol
Ethene and ethanol
Aldehyde
|
| 18 |
The general formula of alkyl halides is |
C<sub>n</sub>H<sub>2n</sub>X
C<sub>n</sub>H<sub>2n-1</sub>X
C<sub>n</sub>H<sub>2n+1</sub>X
C<sub>n</sub>H<sub>2n-2</sub>X
|
| 19 |
The alkyl halide molecule on which a nucleophile attacks is called |
Substrate
Subsituent
Substituted
All of these
|
| 20 |
Which one of the following is not a nuclelphile |
H<sub>2</sub>O
H<sub>2</sub>S
BF<sub>3</sub>
NH<sub>3</sub>
|
| 21 |
The rate of E1reaction depends upon |
The concentration of substrate
The concentration of nucleophile
THe concentration of substrate as well as nucleophile
None of the above
|
| 22 |
Alkyl halides are considered to be very reactive compounds towards nucleophiles because |
They have an electrophilic carbon
They have an electrophilic carbon and a good leaving group
They have an electrophilic carbon and a bad leaving group
They have a nucleophilic carbon and a good leaving group
|
| 23 |
Both E1and E2mechanism can be shown by |
1° - RX
2° - RX
3° - RX
None of these
|
| 24 |
Elimination bimolecular reactions usually obey |
First order kinetics
Second order kinetics
Third order kinetics
Zero order kinetics
|
| 25 |
SN2 reaction can be best carried out with |
Primary alkyl halides
Secondary alkyl halides
Tertiary alkyl halides
All the three
|
| 26 |
Grignad reagent is reactive due to |
The presence of halogen atom
The presence of Mg atom
The polarity of C - Mg bond
None of above
|
| 27 |
When carbon dioxide is passed through the R - Mg - X is produced |
Any carboxylic acid
Propanoic acid
Propanedioic acid
None of these
|
| 28 |
The reactivity order of alkyl halides for a paricular alkyl group is |
Fluoride > chloride > bromide > iodide
Chloride > bromide > fluoride > iodide
Iodide > bromide > chloride > fluoride
Bromide > iodide > chloride > fluoride
|
| 29 |
An electrophile may be |
Positive
Negative
Neutral
Both c and a
|
| 30 |
Grignard reagent is prepared by the reaction of magnesium metal with alkyl halide in the presence of |
Alcohol
Water
Suephuric acid
Dry ether
|