Assertion (A): | Benzene and naphthalene are aromatic hydrocarbons. |
Reason (R): | Benzene and naphthalene contain the same number of delocalized π electrons. |
1. | Both (A) and (R) are True and (R) is the correct explanation of (A). |
2. | Both (A) and (R) are True but (R) is not the correct explanation of (A). |
3. | (A) is a True but (R) is False. |
4. | Both (A) and (R) are False. |
A: Alkyl groups show +l effect.
R: Halogens are -l and +R groups.
1. Both Assertion & Reason are true and the reason is the correct explanation of the assertion.
2. Both Assertion & Reason are true but the reason is not the correct explanation of the assertion.
3. Assertion is a true statement but Reason is false.
4. Both Assertion and Reason are false statements.
Assertion (A): |
2,3-Dimethyl-2-butene is the most stable alkene due to 12- hydrogen atoms. |
Reason (R): | H' is more electronegative than carbon. |
1. | Both (A) and (R) are True and (R) is the correct explanation of (A). |
2. | Both (A) and (R) are True but (R) is not the correct explanation of (A). |
3. | (A) is True but (R) is False |
4. | Both (A) and (R) are False. |
Given below two statements:
Assertion(A): | A compound having a non-superimposable mirror image is optically active. |
Reason(R): | Optically active compound must contain chiral carbon. |
1. | Both (A) and (R) are True and (R) correctly explains (A). |
2. | Both (A) and (R) are True but (R) does not correctly explain (A). |
3. | (A) is True but (R) is False. |
4. | Both (A) and (R) are False. |
Most stable carbanion intermediate in following is :
1. | ![]() |
2. | ![]() |
3. | ![]() |
4. | All of these are equally stable. |
The IUPAC name of the above mentioned compound is -
1. Citric acid
2. 3-Hydroxy pentane-1,5-dioic acid
3. 2-Hydroxypropane-1,2,3-tricarboxylic acid
4. 2-Carboxy-2-hydroxy propane-1,3-dicarboxylic acid
The pair that represents chain isomers is :-
1. | ||
2. | ||
3. | ||
4. |
The pair among the following that does not contain position isomers is -
1. | ![]() |
2. | ![]() |
3. | ![]() |
4. | ![]() |
Which of the following compound exhibit optical isomerism?
1.
2.
3.
4. All of these
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 |