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. | \(HCl + ZnCl_2\), known as Lucas Reagent. | In Lucas test, primary, secondary, and tertiary alcohols are distinguished on the basis of their reactivity with conc.
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 |