Q. No.Carbonyl compound is treated with--- in Clemmensen reduction .
1. Zinc amalgam + HCl
2. Sodium amalgam + HCl
3. Zinc amalgam + nitric acid
4. Sodium amalgam +
Which of the following compounds do not undergo aldol condensation?
| (a) |  |
(b) |  |
| (c) |  |
(d) |  |
Options are as follows:
1. a, b
2. b, d
3. b, c
4. c, d
The product (P) and (Q) of the given reaction are:
| a. | Phenol | b. | Sodium phenoxide |
| c. | Sodium benzoate | d. | Benzophenone |
1. (a, b)
2. (b, c)
3. (c, d)
4. (a, d)
Identify the conversions that are possible with Clemmensen reduction:
a. Benzaldehyde to benzyl alcohol.
b. Cyclohexanone to cyclohexane.
c. Benzoyl chloride to benzaldehyde.
d. Benzophenone to diphenylmethane.
| 1. | a and b | 2. | b and c |
| 3. | c and d | 4. | b and d |
Through which of the following reactions number of carbon atoms can be increased in the chain?
a. Grignard reaction
b. Cannizzaro’s reaction
c. Aldol condensation
d. HVZ reaction
Choose the correct option:
1. (a, b)
2. (b, c)
3. (c, d)
4. (a, c)
Benzophenone can be obtained by:
a. Benzoyl chloride + Benzene
b. Benzoyl chloride + Diphenyl cadmium
c. Benzoyl chloride + Phenyl magnesium chloride
d. Benzene + Carbon monoxide
Choose the correct option
| 1. | (a, b) | 2. | (b, c) |
| 3. | (c, d) | 4. | (a, d) |
Match the common names given in Column I with the IUPAC names given in Column II.
| Column l (Common names) |
Column ll (IUPAC names) |
| A. Cinnamaldehyde | 1. Pentanal |
| B. Acetophenone | 2. Prop-2-enal |
| C. Valeraldehyde | 3. 1-Phenylethanone |
| D. Acrolein | 4. 3-Phenylprop-2-en-al |
Codes:
| A | B | C | D | |
| 1. | 2 | 3 | 4 | 1 |
| 2. | 3 | 1 | 4 | 2 |
| 3. | 1 | 4 | 3 | 2 |
| 4. | 4 | 3 | 1 | 2 |
Match the acids given in Column-I with their correct IUPAC names given in Column-II and mark the appropriate option:
| Column-l (Acids) |
Column-ll (IUPAC names) |
||
| A. | Phthalic acid | 1. | Hexane-1,6-dioic acid |
| B. | Glutaric acid | 2. | Benzene-1,2-dicarboxylic acid |
| C. | Succinic acid | 3. | Pentane-1,5-dioic acid |
| D. | Adipic acid | 4. | Butane-1,4-dioic acid |
Codes:
| A | B | C | D | |
| 1. | 2 | 3 | 4 | 1 |
| 2. | 3 | 1 | 4 | 2 |
| 3. | 1 | 4 | 3 | 2 |
| 4. | 4 | 3 | 2 | 1 |
Match the reactions given in Column-I with the suitable reagents given in Column-II.
| Column-l (Reactions) |
Column-ll
(Reagents)
|
||
| A. | Benzophenone → Diphenylmethane | I. | LiAlH4 |
| B. | Benzaldehyde → 1-Phenylethanol | II. | DlBAL-H |
| C. | Cyclohexanone → Cyclohexanol | III. | Zn(Hg)/Conc. HCl |
| D. | Phenyl benzoate → Benzaldehyde | IV. | CH3MgBr |
Codes:
| A | B | C | D | |
| 1. | II | III | IV | I |
| 2. | III | IV | I | II |
| 3. | I | IV | III | II |
| 4. | IV | III | II | I |
Match the example in Column I with the name of the reaction in Column II.
| Column l (Example) |
Column ll (Reaction) |
A.  |
1. Friedel-Crafts acylation |
B.  |
2. HVZ reaction |
C.  |
3. Aldol condensation |
D.  |
4. Rosenmund Reaction |
| A | B | C | D | |
| 1. | 2 | 3 | 4 | 1 |
| 2. | 3 | 1 | 4 | 2 |
| 3. | 3 | 4 | 1 | 2 |
| 4. | 4 | 1 | 3 | 2 |
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