NEET-UG and JEE Main Chemistry · Class 12
Preparation and properties of amines — NEET & JEE Questions
Preparation and properties of amines is a topic in Organic Compounds Containing Nitrogen, a Class 12 Chemistry chapter of the NEET-UG and JEE Main syllabus. TestBudy holds 12 published NEET-UG and JEE Main questions on Preparation and properties of amines, each with the marking scheme of the real paper.
- questions
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Preparation and properties of amines MCQs with solutions
10 of the 12 published questions on this topic, exactly as they appear in a test. Answers and worked solutions come with your result rather than on this page.
Reduction of a nitro compound such as nitrobenzene commonly gives
- A. an amine
- B. an alcohol
- C. an aldehyde
- D. a carboxylic acid
Reduction of a nitrile generally produces
- A.
- B.
- C.
- D.
The Gabriel phthalimide synthesis is especially useful for preparing
- A. primary aliphatic amines
- B. secondary amines only
- C. tertiary amines only
- D. quaternary ammonium salts
Amines react with mineral acids such as HCl to form
- A. ammonium salts
- B. alkenes
- C. ethers
- D. carboxylic acids
What is the major organic product when ethanenitrile, , is completely reduced?
- A. Methanamine
- B. Ethanamine
- C. Propanamine
- D. Ethanal
Aniline reacts with hydrochloric acid. Which product is formed?
- A. Anilinium chloride
- B. Chlorobenzene
- C. Benzamide
- D. Phenol
Which reagent can reduce nitrobenzene to aniline?
- A.
- B. solution
- C. dilute only
- D. water only
A primary amide is converted to a primary amine containing one fewer carbon atom by
- A. Hofmann bromamide degradation
- B. simple hydrolysis
- C. oxidation with
- D. esterification
Which sequence converts nitrobenzene into aniline and then into an anilinium salt?
- A. Reduction, followed by treatment with HCl
- B. Oxidation, followed by treatment with NaOH
- C. Hydrolysis, followed by bromination
- D. Reduction, followed by treatment with Na metal
An amide undergoes Hofmann bromamide degradation. Which amine is formed?
- A. Methanamine
- B. Ethanamine
- C. Propanamine
- D. Butanamine
Common mistakes in Preparation and properties of amines
Recorded against questions in this topic that are not shown above, so none of these points at an answer you can see on this page.
- Assumes direct alkylation stops automatically after the first substitution.
- Chooses an amide or nitro compound without matching both the molecular formula and the carbon count of the reduced amine.
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