| 1. | Sublimation | 2. | Distillation |
| 3. | Chromatography | 4. | Crystallization |
| List-I (Molecule) |
List-II
(Number and types of bond/s between two carbon atoms)
|
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| A. | Ethane | I. | \(\small{\mathrm{One ~\sigma-bond~ and~ Two~ \pi-bonds}}\) |
| B. | Ethene | II. | \(\text { Two } \pi \text {-bonds }\) |
| C. | Carbon molecule, \(\mathrm{C} _2\) |
III. | \(\text { One } \sigma \text {-bond }\) |
| D. | Ethyne | IV. | \(\small{\mathrm{One ~\sigma-bond ~and ~One~ \pi-bond}}\) |
| 1. | A-IV, B-III, C-II, D-I | 2. | A-III, B-IV, C-II, D-I |
| 3. | A-III, B-IV, C-I, D-II | 4. | A-I, B-IV, C-II, D-III |
| 1. | ![]() |
2. | ![]() |
| 3. | ![]() |
4. | ![]() |
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2. | ![]() |
| 3. | ![]() |
4. | ![]() |
| 1. | 2. | ||
| 3. | 4. |
| Statement I: | In an organic compound, when inductive and electromeric effects operate in opposite directions, the inductive effect predominates. |
| Statement II: | Hyperconjugation is observed in o-xylene. |
| List-I (Mixtures/Sample) |
List-II (Technique used for purification) |
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| A. | Glycerol from spent lye | (I) | Steam distillation |
| B. | Chloroform + Aniline | (II) | Fractional distillation |
| C. | Fractions of crude oil | (III) | Distillation under reduced pressure |
| D. | Aniline+water | (IV) | Distillation |
| Options: | (A) | (B) | (C) | (D) |
| 1. | III | IV | II | I |
| 2. | IV | II | I | III |
| 3. | I | II | III | IV |
| 4. | I | III | II | IV |