The group that activates the benzene ring towards electrophilic substitution reaction is:
1. | OH | 2. | NO2 |
3. | CN | 4. | COOH |
The alkoxy group in aryl alkyl ethers activates the benzene ring towards:
1. Nucleophilic addition reaction
2. Electrophilic addition reaction
3. Nucleophilic substitution reaction
4. Electrophilic substitution reaction
An appropriate set of reactants for the preparation of 1-methoxy-4-nitrobenzene is/are :
1. | |
2. | |
3. | |
4. |
In Kolbe’s reaction,
the product formed will be:
1. Para-salicylic aldehyde
2. Ortho-salicylic aldehyde
3. Para-salicylic acid
4. Ortho-salicylic acid
In Reimer-Tiemann reaction,
the product will be:
1. ortho-Salicylaldehyde
2. para-Salicylaldehyde
3. meta-Salicylaldehyde
4. All of the above
In Williamson ether synthesis, the major product would be:
1. 1-Methoxypropane
2. 2-Methoxypropane
3. 3-Methoxypropane
4. All of the above
Unsymmetrical ether will be the product in:
1. Kolbe’s reaction.
2. Reimer-Tiemann reaction.
3. Williamson ether synthesis.
4. None of the above.