The correct order of the acidic strength for the above compounds is -
(I) | (II) | (III) |
1. I > II > III
2. III > I > II
3. II > III > I
4. I > III > II
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"A" in the reaction below is:
1. | Chlorobenzene | 2. | 1,2-Dichlorobenzene |
3. | 1,3-dichlorobenzene | 4. | None of these |
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The most acidic compound among the following is:
1. | 2. | ||
3. | 4. |
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Potassium permanganate reagent is used for -
1. Oxidation of primary alcohol to carboxylic acid.
2. Oxidation of primary alcohol to aldehyde.
3. Bromination of phenol to 2,4,6-tribromophenol.
4. Dehydration of propan-2-ol to propene.
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The most acidic compound among the following is:
1. | 2. | ||
3. | 4. |
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Match the structures of the compounds given in Column I with the name of the compounds given in Column II.
Column I | Column II | ||
A. | 1. | Phenetole | |
B. | 2. | o-Cresol | |
C. | 3. | Catechol | |
D. | 4. | Resorcinol |
Codes
A | B | C | D | |
1. | 2 | 4 | 1 | 3 |
2. | 3 | 1 | 4 | 2 |
3. | 1 | 4 | 3 | 2 |
4. | 4 | 3 | 2 | 1 |
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Phenol in a set of reactions (as captured below) yielded a product Z.
\(\text{Phenol}\ \xrightarrow{\text{Zn Dust}}\ \text{X}\ \xrightarrow[\text{Anhy. }{AlCl_3}]{CH_3Cl}\ Y\)
\( Y\ \xrightarrow[KMnO_4]{\text{Alkaline}}\ Z\)
The structure of the product Z would be:
1. Toluene
2. Benzaldehyde
3. Benzoic acid
4. Benzene
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The reagent used for the bromination of phenol to 2,4,6-tribromophenol is/are:
1. Bromine water
2. Br2, CS2
3. Br2, CCl4
4. AgBr
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The most acidic compound among the following is:
1. | 2. | ||
3. | 4. |
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The strongest acid among the following aromatic compounds is -
1. | p-Chlorophenol | 2. | p-Nitrophenol |
3. | m-Nitrophenol | 4. | o- Nitrophenol |
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