ICSE Class 10 Amines (Organic Compounds Containing Nitrogen) — Mock Test (2027)
Free online mock test for Amines (Organic Compounds Containing Nitrogen) (ICSE Class 10 Chemistry) — 75 competency-based questions based on the latest CISCE 2027 syllabus, with instant marking. Try the samples below, then take the full test free.
What to expect: This mock test covers key concepts from the Amines (Organic Compounds Containing Nitrogen) chapter — including application-based and competency-focused questions aligned with how ICSE actually sets the paper.
Tip: Attempt without notes first to identify gaps, then review explanations for any wrong answers. Retake after a few days for best retention.
Sample questions
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1.Arrange in INCREASING order of basic strength: C2H5NH2, C6H5NH2, NH3, C6H5CH2NH2 and (C2H5)2NH.
- A.C6H5NH2 < NH3 < C6H5CH2NH2 < C2H5NH2 < (C2H5)2NH
- B.(C2H5)2NH < C2H5NH2 < C6H5CH2NH2 < NH3 < C6H5NH2
- C.NH3 < C6H5NH2 < C6H5CH2NH2 < C2H5NH2 < (C2H5)2NH
- D.C6H5CH2NH2 < C6H5NH2 < NH3 < C2H5NH2 < (C2H5)2NH
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2.The conversion of a primary aromatic amine into a diazonium salt is called:
- A.Diazotisation
- B.Acylation
- C.Ammonolysis
- D.Coupling
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3.Assertion (A): The amine formed by the Hoffmann bromamide degradation of an amide contains one carbon atom less than the amide. Reason (R): In the Hoffmann bromamide reaction an alkyl or aryl group migrates from the carbonyl carbon of the amide to the nitrogen atom.
- A.Both A and R are true and R is the correct explanation of A
- B.Both A and R are true but R is NOT the correct explanation of A
- C.A is true but R is false
- D.A is false but R is true
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4.Assertion (A): In trimethylamine the C-N-C bond angle is less than 109.5 degrees. Reason (R): The unshared pair of electrons on nitrogen exerts a repulsion that compresses the bond angle below the regular tetrahedral value.
- A.Both A and R are true and R is the correct explanation of A
- B.Both A and R are true but R is NOT the correct explanation of A
- C.A is true but R is false
- D.A is false but R is true
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5.Aniline reacts with bromine water at room temperature to give as the major product:
- A.2,4,6-Tribromoaniline (white precipitate)
- B.p-Bromoaniline only
- C.o-Bromoaniline only
- D.Bromobenzene
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