Amines Preparation Properties
High-Yield Trend
Questions 17 MCQs
Propanoic acid gives a series of reactions as given below.
The structure of D would be:
1.
2.
3.
4.
Which of the following compounds has a higher basic character than aniline?
1. Diphenylamine
2. Triphenylamine
3. p-nitroaniline
4. Benzylamine
What is the product formed in the below reaction?
| 1. | 2. | ||
| 3. | 4. |
The reagent that is used to convert acetamide into methyl amine is:
1. NaOH-Br2
2. Soda lime
3. Hot conc. H2SO4
4. PCl5
The incorrect statement among the following regarding the primary amine is:
| 1. | Alkyl amines are stronger bases than aryl amines |
| 2. | Alkyl amines react with nitrous acid to produce alcohols |
| 3. | Aryl amines react with nitrous acid to produce phenols |
| 4. | Alkyl amines are stronger bases than ammonia |
The number of structural isomers possible from the molecular formula C3H9N are:
| 1. | Four (4) | 2. | Five (5) |
| 3. | Two (2) | 4. | Three (3) |
Mark the reaction that does not yield aniline from the given options:
| 1. | Hydrolysis of phenyl isocyanide with an acidic solution |
| 2. | Degradation of benzamide with bromine in alkaline solution |
| 3. | Reduction of nitrobenzene with H2/Pd in ethanol |
| 4. | Treatment of potassium salt of phthalimide with chlorobenzene followed by hydrolysis in an aqueous NaOH solution |
What is the name of the following reaction?
1. Friedel-Crafts reaction
2. Perkins reaction
3. Acetylation reaction
4. Schotten-Baumann reaction
The correct increasing order of basic strength of the given molecules is:
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| (I) | (II) | (III) |
1. III < I < II
2. III < II < I
3. II < I < III
4. II < III < I
Mark the correct reaction among the following to convert acetamide to methenamine:
1. Hoffmann bromamide reaction
2. Stephens reaction
3. Gabriels phthalimide synthesis
4. Carbylamine reaction
The nitration of aniline in a strong acidic medium results in the formation of m-nitroaniline because:
| 1. | In spite of substituents, the nitro group always goes to only the m-position. |
| 2. | In electrophilic substitution reactions, the amino group is meta-directive. |
| 3. | In the absence of substituents, the nitro group always goes to only m-position. |
| 4. | In an acidic (strong) medium, aniline is present as an anilinium ion. |
1. CH3NH2 > (CH3)2NH > (CH3)3N
2. (CH3)2NH > CH3NH2 > (CH3)3N
3. (CH3)3N > CH3NH2 > (CH3)2NH
4. (CH3)2NH > (CH3)3N > CH3NH2
| 1. | Ethylamine | 2. | Methylamine |
| 3. | Propylamine | 4. | Aniline |
| 1. | |
| 2. | ![]() |
| 3. | ![]() |
| 4. | ![]() |
| Statement I: | Aniline does not undergo Friedel-Crafts alkylation reaction. |
| Statement II: | Aniline cannot be prepared through Gabriel synthesis. |
| 1. | Both Statement I and Statement II are incorrect. |
| 2. | Statement I is correct and Statement II is incorrect. |
| 3. | Statement I is incorrect and Statement II is correct. |
| 4. | Both Statement I and Statement II are correct. |
| 1. | Butylamine | 2. | Butanamide |
| 3. | Bromobutanoic acid | 4. | Propylamine |
| 1. | N-ethylethanamine > ethanamine > N -methylaniline > benzenamine |
| 2. | benzenamine > ethanamine > N -methylaniline >N-ethylethanamine |
| 3. | N -methylaniline > benzenamine > ethanamine >N-ethylethanamine |
| 4. | N-ethylethanamine > ethanamine > benzenamine >N-methylaniline |
Preparing Amines Preparation Properties for NEET
Amines Preparation Properties is a specific sub-topic that frequently appears in the NEET examination. Understanding the underlying principles and practicing targeted questions is key to mastering this concept.
The questions compiled above are previous year questions (PYQs) directly related to Amines Preparation Properties. Practicing these specific questions helps you understand the difficulty level and the examiner's approach to this topic.
Topic Frequently Asked Questions
Is Amines Preparation Properties a high-weightage topic?
You can refer to the priority and consistency badges at the top of this page. High priority topics should be thoroughly revised multiple times before the exam.
Should I memorize the solutions?
No, it is highly recommended to understand the core concept and methodology behind each solution rather than memorizing them, as exact questions are rarely repeated, but the concepts definitely are.





