| 1. | Covalent form to covalent form |
| 2. | Ionic form to ionic form |
| 3. | Covalent form to ionic form |
| 4. | Ionic form to covalent form |
| 1 | ![]() |
| 2. | ![]() |
| 3. | ![]() |
| 4. | ![]() |

| Statement I: | trans-But-2-ene upon treatment with Br2 in CCl4 gives the following product.![]() |
| Statement II: | cis-But-2-ene upon treatment with alkaline KMnO4 gives the following product.![]() |
| 1. | Statement I is incorrect but Statement II is correct |
| 2. | Both Statement I and Statement II are correct |
| 3. | Both Statement I and Statement II are incorrect |
| 4. | Statement I is correct but Statement II is incorrect |
| A. | \(CH_3CH_2OCH_2CH_3\) |
| B. | \(CH_3CH_2OH\) |
| C. | \(CH_3COCH_3\) |
| D. | \(CH_3COOH\) |
| 1. | A < C < B < D |
| 2. | A < B < C < D |
| 3. | C < A < D < B |
| 4. | C < A < B < D |
| 1. | hepta-1,6-diene |
| 2. | hepta-1,3-diene |
| 3. | hepta-1,4-diene |
| 4. | hepta-1,5-diene |
| 1. | M and N are stereoisomers |
| 2. | K and L are geometrical isomers |
| 3. | K and L are enantiomers |
| 4. | M and N are geometrical isomers |
| 1. | \(\mathrm{Na}+\mathrm{X} \underset{\Delta}{\longrightarrow}+\mathrm{NaX} \) |
| 2. | \(2 \mathrm{CuO}+\mathrm{C} \xrightarrow[\Delta]{} 2 \mathrm{Cu}+\mathrm{CO}_2 \) |
| 3. | \(\mathrm{Na}+\mathrm{C}+\mathrm{N} \xrightarrow[\Delta]{} \mathrm{NaCN} \) |
| 4. | \(2 \mathrm{Na}+\mathrm{S} \xrightarrow[\Delta]{} \mathrm{Na}_2 \mathrm{~S}\) |
| List-I (Mixture) |
List-II (Method of Separation) |
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| A. | \( \mathrm{CHCl}_3+ \mathrm{C}_6 \mathrm{H}_5 \mathrm{NH}_2 \) | I. | Distillation under reduced pressure |
| B. | Crude oil in petroleum industry | II. | Steam distillation |
| C. | Glycerol from spent-lye | III. | Fractional distillation |
| D. | Aniline-water | Iv. | Simple distillation |
| 1. | Sublimation | 2. | Distillation |
| 3. | Chromatography | 4. | Crystallization |