Arrange the following in order of their reactivity toward electrophilic substitution reaction:
I. | ![]() |
II. | ![]() |
III. | ![]() |
Iv. | ![]() |
1. | I > II > III > IV | 2. | IV > III > II > I |
3. | II > I > IV > III | 4. | II > I > III > IV |
The major product in the given reaction is-
1.
2.
3.
4.
Which of the following compound is soluble in aqueous NaOH?
1.
2.
3.
4.
Which of the following compound requires minimum energy for free rotation across double bond between ring :
1. | ![]() |
2. | ![]() |
3. | ![]() |
4. | ![]() |
Which of the following is not nucleophile:-
1.
2.
3.
4.
Correct order of acidic strength for following is:-
1. I > II > III > IV
2. I > III > II > IV
3. IV > III > I > II
4. III > I > II > IV
Which of the following although have -hydrogen but does not show tautomerism :-
1.
2.
3.
4.
The molecule that exhibits non-planarity is:
1. | ![]() |
2. | ![]() |
3. | ![]() |
4. | ![]() |
The aromatic compound among the following is:-
1. | ![]() |
2. | ![]() |
3. | ![]() |
4. | ![]() |
Which carbocation is the most stable among the options provided?
1. | 2. | ||
3. | 4. |