Practice · Chemistry · 2025 syllabus · R3.4
IB Chemistry R3.4 Electron-pair sharing reactions: practice questions
10 exam-style questions on R3.4 Electron-pair sharing reactions, SL and HL, 10 marked HL: 6 multiple choice and 4 structured. Each one comes with the mark scheme, a model answer and the reasoning behind every mark. Free with your email.
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R3.4-01 · Paper 1A style · multiple choice · 1 mark · HL
Role of ammonia in substitution
What is the role of ammonia in this reaction?
CH3CH2Br + NH3 → CH3CH2NH2 + HBr [1]
- Electrophile and Lewis acid
- Nucleophile and Lewis acid
- Electrophile and Lewis base
- Nucleophile and Lewis base
Show the answer and the reasoning
Answer: D. D is correct. The lone pair on nitrogen attacks the carbon bonded to bromine, forming a new bond: ammonia is a nucleophile, and because it donates an electron pair it is also a Lewis base. A and C: an electrophile accepts an electron pair. B: a Lewis acid accepts an electron pair.
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The 10 questions in R3.4
- R3.4-01 Role of ammonia in substitution
- R3.4-02 The electrophile that attacks benzene
- R3.4-03 Major product from HBr
- R3.4-04 Fastest halogenoalkane
- R3.4-05 Features of SN1
- R3.4-06 Which are Lewis acids
- R3.4-07 An SN2 mechanism with curly arrows
- R3.4-08 Adding HBr to propene
- R3.4-09 Telling SN1 from SN2
- R3.4-10 Why benzene substitutes
More of R3 What are the mechanisms of chemical change?
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Every Biology and Chemistry question here is original, written for practice in the style of the papers set since the 2025 syllabus, with invented data. Developed independently from the International Baccalaureate Organization, which has not endorsed it. Found a mistake? Email vytis@limeadmissions.com with the question id.