| 1. | \(\text { (i) } \mathrm{BH}_3\) | 2. | \(\text { (i) } \mathrm{BH}_3\) |
| \((ii) \mathrm{H}_2 \mathrm{O}_2 / \stackrel{\ominus}{\mathrm{OH}}\) | \((ii) \mathrm{H}_2 \mathrm{O}_2 / \stackrel{\ominus}{\mathrm{OH}}\) | ||
| \(\text { (iii) } \mathrm{P C C}\) | \(\text { (iii) alk. } \mathrm{KMnO}_4\) | ||
| \(\text { (iv) } \mathrm{H}_3 \mathrm{O}^{+}\) | |||
| 3. | \(\text { (i) } \mathrm{H}_2 \mathrm{O} / \mathrm{H}^{+}\) | 4. | \(\text { (i) } \mathrm{H}_2 \mathrm{O} / \mathrm{H}^{+}\) |
| \(\text { (ii) } \mathrm{P C C}\) | \(\text { (ii) } \mathrm{CrO}_3\) |
| 1. | ![]() |
| 2. | ![]() |
| 3. | ![]() |
| 4. | \(\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{CH}_2-\mathrm{CH}_2 \mathrm{OH}\) |
| 1. | ![]() |
2. | ![]() |
| 3. | ![]() |
4. | ![]() |
| 1. | 2. | ||
| 3. | 4. |
| 1. | |
| 2. | |
| 3. | |
| 4. |
| 1. | \(B_2H_6 \) | 2. | \(LiAlH_4 \) |
| 3. | \(NaBH_4 \) | 4. | \(H_2/Pd \) |
| 1. | 2. | ||
| 3. | 4. |
| I: | The acidic strength of monosubstituted nitrophenol is higher than phenol because of electron withdrawing nitro group. |
| II: | o-Nitrophenol, m-nitrophenol and p-nitrophenol will have same acidic strength as they have one nitro group attached to the phenolic ring. |
| 1. | I is incorrect but II is correct. |
| 2. | Both I and II are correct. |
| 3. | Both I and II are incorrect. |
| 4. | I is correct but II is incorrect. |
| Statement I: | In Lucas test, primary, secondary, and tertiary alcohols are distinguished on the basis of their reactivity with conc. \(HCl + ZnCl_2\), known as Lucas Reagent. |
| Statement II: | Primary alcohols are most reactive and immediately produce turbidity at room temperature on reaction with Lucas Reagent. |
| 1. | I is incorrect but II is correct |
| 2. | Both I and II correct |
| 3. | Both I and II are incorrect |
| 4. | I is correct but II is incorrect |