Which of the following is the most correct electron displacement for a nucleophilic reaction to take place?
1. | |
2. | |
3. | |
4. |
Some meta-directing substituents in aromatic substitution are given.
Most deactivating group among the following is:
1. –SO3H
2. –COOH
3. –NO2
4. –C≡N
Among the following compounds the one that is most reactive towards electrophilic nitration is:
1. Benzoic acid
2. Nitrobenzene
3. Toluene
4. Benzene
Among cyclohexanol (I), acetic acid (II), 2, 4, 6-trinitrophenol (III) and phenol (IV) the correct order of decreasing acidic character will be:
1. | III>II>IV>I | 2. | II>III>I>IV |
3. | II>III>IV>I | 4. | III>IV>II>I |
Which one is most reactive towards SN1 reaction?
1.
2.
3.
4.
Which one of the following is most reactive towards electrophilic attack?
1. | 2. | ||
3. | 4. |
In a SN2 substitution reaction of the type
\(\mathrm{R}-\mathrm{Br}+\mathrm{Cl}^{-} \xrightarrow{\mathrm{DMF}} \mathrm{R}-\mathrm{Cl}+\mathrm{Br}^{-}\)
one of the following that has the highest relative rate is:
1. | \(\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{CH}_2 \mathrm{Br}\) | 2. | |
3. | 4. | \(\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{Br}\) |
For the above-given reaction, A (Predominantly) is:
1. | 2. | ||
3. | 4. |