Learning objective
Predict major products from addition to unsymmetrical alkenes.
Read the explanation, check the common trap, then practise with flashcards and questions.
At a glance
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Flashcards
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Questions
Topic
Alkenes
Subtopic
Electrophilic addition
Study support
Understand this objective
Quick explanation
Predict major products from addition to unsymmetrical alkenes
- This point belongs to Alkenes, especially Electrophilic addition.
- You need to be able to predict major products from addition to unsymmetrical alkenes.
- The key ideas to know are from, predict, and addition.
- Use the linked flashcards and practice questions to check recall, then practise applying the idea in an exam-style answer.
Key concepts
Why it matters
This objective helps connect Electrophilic addition to exam-style questions, flashcards, and revision notes for Alkenes.
Quick student answer
When propene (C3H6) undergoes electrophilic addition with HBr, which of the following is the major product?
Direct answer
2-bromopropane
Key terms
- Electrophilic addition: A reaction where an electrophile reacts with a nucleophile, resulting in the addition of atoms or groups across a double bond.
- Carbocation: An ion with a positively charged carbon atom, which is an important intermediate in many organic reactions.
Common trap
Ignoring Markovnikov's rule: Always apply Markovnikov's rule to determine the major product in reactions involving unsymmetrical alkenes.
Related questions
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Flashcard prompts
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Revision tools
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Revision notestopic notes
Open the full topic revision notes when you are ready to review this objective in context.
Open revision notesRelated learning objectives
- Describe alkenes as unsaturated hydrocarbons.
Structure, bonding and reactivity
- Explain bonding in alkenes using sigma and pi bonds.
Structure, bonding and reactivity
- Explain why the C=C bond is attacked by electrophiles.
Structure, bonding and reactivity
- Use bromine water to test for unsaturation.
Structure, bonding and reactivity
- Outline electrophilic addition to alkenes with hydrogen bromide.
Electrophilic addition
