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Electrophilic addition mechanismsEdexcel International A Level Chemistry: Mind map

What this mind map covers

  • Electrophiles
  • Curly arrows
  • Mechanism
  • Carbocation stability
  • Propene + HBr

Exam questions on Electrophilic addition mechanisms

  1. A student is learning how electrophiles such as bromine and hydrogen bromide react with the C=C bond of ethene, even though a bromine molecule is non-polar.
    Define the term electrophile, and identify the atom in hydrogen bromide that acts as the electrophile in its reaction with ethene.2 marks
  2. 2-Methylpropene, (CH₃)₂C=CH₂, reacts with hydrogen bromide by a mechanism that involves a carbocation intermediate.
    Explain why a tertiary carbocation is more stable than a primary carbocation.2 marks
  3. Propene reacts with hydrogen bromide to give 2-bromopropane as the major product and 1-bromopropane as the minor product. Ethene also reacts with hydrogen bromide.
    Explain why 2-bromopropane is the major product of the reaction of propene with hydrogen bromide.3 marks
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Written by the Exaim team, led by Shaun Daswani (Head of Upper Secondary, Improve ME Institute; MSc Financial Mathematics, Imperial College London; BSc, UCL) and Jason Daswani (operational lead, Improve ME Institute; LSE).