The increasing order of reactivity of the following compounds towards acid-catalyzed dehydration is:
1. | 2. | ||
3. | 4. |
1. | (II) < (III) < (I) < (IV) | 2. | (II) < (I) < (III) < (IV) |
3. | (I) < (III) < (IV) < (II) | 4. | (III) < (I) < (II) < (IV) |
The correct order of acidic strength of the following molecules is:
1. | |
2. | |
3. | |
4. |
The major products formed in the following reaction are:
1. | 2. | ||
3. | 4. |
Match the reagents (List-I) with the products (List-II) obtained from phenol:
List-I | List-II | ||
(A) | (i) NaOH (ii) CO2 (iii) H+ |
(I) | Benzoquinone |
(B) | (i) Aqueous NaOH + CHCl3 (ii) H+ |
(II) | Benzene |
(C) | \(\Delta\) | Zn dust,(III) | Salicylaldehyde |
(D) | Na2Cr2O7, H2SO4 | (IV) | Salicylic acid |
(A) | (B) | (C) | (D) | |
1. | (III) | (IV) | (I) | (II) |
2. | (II) | (I) | (IV) | (III) |
3. | (IV) | (III) | (II) | (I) |
4. | (IV) | (II) | (I) | (III) |
1. | Aniline, NaNO2 + HCl, H2O, heating |
2. | Cumene, O2, H3O+ |
3. | |
4. |
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 |
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 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. |
1. | 2. | ||
3. | 4. |
1. | |
2. | |
3. | |
4. |