1. | 2. | ||
3. | 4. |
1. | 2. | ||
3. | 4. |
1. | |
2. | |
3. | |
4. |
1. | (B), (C) and (D) only | 2. | (B), (D) and (E) only |
3. | (A), (B) and (C) only | 4. | (A), (B) and (E) only |
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 |
I: | The product of the reaction of phenol with bromine depends on the nature of the solvent. |
II: | The reaction of phenol with bromine in CHCl3 gives a monosubstituted bromo derivative whereas the reaction of phenol with bromine water yields a trisubstituted bromo derivative of phenol. |
In light of the above statements, choose the most appropriate answer from the options given below:
1. | I is correct and II is incorrect |
2. | I is incorrect and II is correct |
3. | Both I and II are correct |
4. | Both I and II are incorrect |
The increasing order of reactivity of the following compounds towards acid-catalyzed dehydration is:
1. | \(CH_3-CH_2-OH \) | 2. | |
3. | 4. | \(CH_3-C(CH_3)_2-OH \) |
1. | (II) < (III) < (I) < (IV) | 2. | (II) < (I) < (III) < (IV) |
3. | (I) < (III) < (IV) < (II) | 4. | (III) < (I) < (II) < (IV) |