Assertion (A): | Simple distillation can help in separating a mixture of propan-1-ol (boiling point 97°C ) and propanone (boiling point 56°C ). |
Reason (R): | Liquids with a difference of more than 20°C in their boiling points can be separated by simple distillation. |
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. | (A) is False but (R) is True. |
Assertion (A): | Energy of resonance hybrid is equal to the average of energies of all canonical forms. |
Reason (R): | Resonance hybrid cannot be presented by a single structure. |
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. | (A) is False but (R) is True. |
Assertion (A): | Pent-1-ene and pent-2-ene are position isomers. |
Reason (R): | Position isomers differ in the position of a functional group or a substituent. |
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. | (A) is False but (R) is True. |
Given below are two statements:
Assertion (A): | All the carbon atoms in H2C = C = CH2 are sp2-hybridised. |
Reason (R): | In this molecule, all the carbon atoms are attached to each other by double bonds. |
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. | (A) is False but (R) is True. |
Assertion (A): | Sulphur present in an organic compound can be estimated quantitatively by the Carius method. |
Reason (R): | Sulphur is separated easily from other atoms in the molecule and gets precipitated as a light yellow solid. |
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. | (A) is False but (R) is True. |
Given below are two statements:
Assertion (A): | Components of a mixture of red and blue inks can be separated by distributing the components between stationary and mobile phases in paper chromatography. |
Reason (R): | The colored components of inks migrate at different rates because paper selectively retains different components according to the difference in their partition between the two phases. |
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. | (A) is False but (R) is True. |
Match Column I with Column II.
Column I | Column II | ||
A. | Dumas method | 1. | AgNO3 |
B. | Kjeldahl’s method | 2. | Silica gel |
C. | Carius method | 3. | Nitrogen gel |
D. | Chromatography | 4. | Ammonium sulphate |
Choose the correct answer from the options given below:
A | B | C | D | |
1. | 3 | 4 | 1 | 2 |
2. | 1 | 2 | 3 | 4 |
3. | 1 | 4 | 3 | 2 |
4. | 4 | 1 | 3 | 2 |
Match the terms mentioned in Column-I with the terms in Column-II.
Column-I (Term) | Column-II (Definition) | ||
A. | Carbocation | (i) | Species that can receive a pair of electrons. |
B. | Nucleophile | (ii) | Conjunction of electrons of \(C-H ~\sigma-\) bond with the empty p-orbital present in adjacent positively charged carbon. |
C. | Hyperconjugation | (iii) | sp2 hybridised carbon with empty p-orbital. |
D. | Electrophile | (iv) | Species that can donate a pair of electrons. |
Options: | A | B | C | D |
1. | (iii) | (iv) | (ii) | (i) |
2. | (i) | (ii) | (iii) | (iv) |
3. | (i) | (iv) | (iii) | (ii) |
4. | (iv) | (i) | (iii) | (ii) |
Which carboxylate ion among the following is the most stable?
1. | ![]() |
2. | ![]() |
3. | ![]() |
4. | ![]() |
The correct order of decreasing stability of the following carbocations is:
I | \( \begin{aligned} &~~~~~~~~~~~~\oplus\\ & CH_3 - CH-CH_3 \end{aligned}\) |
II | \( \begin{aligned} &~~~~~~~~~~~~\oplus\\ & CH_3 - CH-OCH_3\end{aligned}\) |
III | \( \begin{aligned} & ~~~~~~~~~~~~\oplus\\ &CH_3 - CH-CH_2- OCH_3\end{aligned}\) |
1. | II > I > III | 2. | I > II > III |
3. | II < I < III | 4. | I < II < III |