The major product formed in the given reaction is:
1. | 2. | ||
3. | 4. |
The maximum number of isomers that can result from monobromination of 2-methyl-2-pentene with N-bromosuccinimide in boiling is
1. 1
2. 2
3. 3
4. 4
The order of SN1 reactivity in the aqueous acetic acid solution for the given compounds is:
1. I > II > III
2. I > III > II
3. III > II > I
4. III > I > II
Select the most correct statement among the following:
1. | SN1 mechanism takes place in non-polar solvents. |
2. | SN2 mechanism in chiral substrates gives racemic mixture as products. |
3. | SN1 mechanism is encouraged by polar solvents. |
4. | The solvent never influences the mechanism. |
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The compound which undergoes hydrolysis on just warming with water and forms the corresponding hydroxyl derivative is:
1. 2, 4, 6-Trinitrochlorobenzene
2. 2-Chloro-1-butene
3. 2-Chloro-2-methyl butane
4. 2, 4-Dimethoxychlorobenzene
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The compound that is most reactive with alcoholic KOH is
1.
2.
3.
4.
(i) Chloro benzene is mono-nitrated to M
(ii) Nitrobenzene is mono-chlorinated to N
(iii) Anisole is mono-nitrated to P
(iv) 2-nitro chlorobenzene is mono-nitrated to Q
Out of M, N, P, and Q, the compound that undergoes reaction with aqueous NaOH fastest is:
1. M
2. N
3. P
4. Q
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If there is no rotation of plane-polarized light by a compound in a specific solvent, thought to be chiral, it may mean that :
1. The compound is certainly a chiral
2. The compound is certainly meso
3. There is no compound in the solvent
4. The compound may be a racemic mixture
In which of the following compounds, the C—Cl bond ionization shall give the most stable carbonium ion?
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Chlorobenzene is prepared commercially by:
1. Grignard reaction
2. Raschig process
3. Wurtz-Fittig reaction
4. Friedel-Crafts reaction