OxfordAQA International A Level Chemistry
OxfordAQA International A Level Chemistry 3.3.4 Alkenes Exam Questions
Free OxfordAQA International A Level Chemistry revision for 3.3.4 Alkenes: what you need to know, common mistakes and exam-style questions with answers. Covers electrophilic addition with HBr, sulfuric acid and bromine, carbocation stability, the bromine water test, addition polymers including PVC, and epoxyethane.
Practise 3.3.4 Alkenes with past papers
Once you have learnt this topic, find the 3.3.4 Alkenes questions in real OxfordAQA International A Level Chemistry past papers and mark them with the mark scheme. Doing lots of real questions is the quickest way to learn how examiners ask about each idea.
About OxfordAQA International A Level Chemistry 3.3.4 Alkenes
Alkenes is a Unit 2 organic topic about compounds with a C=C double bond. You need to explain why alkenes undergo electrophilic addition and draw mechanisms for reactions with hydrogen bromide, sulfuric acid and bromine. You also need to use carbocation stability to explain major and minor products, and use bromine water as a test for unsaturation. The OxfordAQA specification includes addition polymers, PVC and plasticisers, and the production of epoxyethane by partial oxidation of ethene, with its reactions with water and alcohols to make antifreeze and surfactants and the hazards involved. It links to halogenoalkanes, alcohols and polymers at A2.
What you need to know
- Structure and reactivity The C=C double bond is a region of high electron density, so it attracts electrophiles, which are electron pair acceptors.
- Electrophilic addition With HBr, the pi bond attacks the H of H-Br, forming a carbocation and Br-, which then bonds to the carbocation. Bromine and concentrated sulfuric acid also add across the double bond.
- Major and minor products For unsymmetrical alkenes, the major product forms via the more stable carbocation. Tertiary carbocations are more stable than secondary, which are more stable than primary, because alkyl groups release electrons.
- Test for alkenes Bromine water is decolourised from orange to colourless by an alkene.
- Addition polymers Alkenes join to form addition polymers, which are unreactive because they are saturated. PVC is made from chloroethene, and plasticisers are added to make it flexible by allowing chains to slide over each other.
- Epoxyethane Epoxyethane is made by partial oxidation of ethene with oxygen and a silver catalyst. It reacts with water to make ethane-1,2-diol (antifreeze) and with alcohols to make surfactants; it is toxic and flammable, so it must be handled carefully.
Common mistakes in 3.3.4 Alkenes
- Drawing the first curly arrow from a carbon atom. It starts from the C=C double bond and goes to the electrophile.
- Saying the minor product is formed via the more stable carbocation. The major product comes from the more stable carbocation.
- Saying bromine water goes clear. Say it changes from orange to colourless.
- Saying addition polymers are unreactive because they are long. They are unreactive because the chains are saturated with strong C-C and C-H bonds.
Try three 3.3.4 Alkenes exam-style questions
1. Outline the mechanism for the reaction of propene with hydrogen bromide to form the major product. (4 marks)
Show the mark scheme answer
Curly arrow from C=C to H of HBr; curly arrow from H-Br bond to Br; secondary carbocation CH3C+HCH3 formed; curly arrow from lone pair on Br- to C+, giving 2-bromopropane.
2. Explain why 2-bromopropane is the major product. (2 marks)
Show the mark scheme answer
It forms via a secondary carbocation; which is more stable than the primary carbocation because of more electron-releasing alkyl groups.
3. Draw the repeating unit of poly(chloroethene). (1 mark)
Show the mark scheme answer
-[CH2-CHCl]- with bonds extending from each end of the two-carbon unit.
3.3.4 Alkenes FAQs
What does OxfordAQA International A Level Chemistry 3.3.4 Alkenes cover?
It covers electrophilic addition with HBr, sulfuric acid and bromine, carbocation stability, the bromine water test, addition polymers including PVC, and epoxyethane.
Which unit is 3.3.4 Alkenes examined in?
It is examined in Unit 2, the second International AS paper, which covers organic and physical chemistry. The Unit 5 practical and synoptic paper at A2 can also assess it.
What is the role of plasticisers in PVC?
Plasticisers are small molecules that fit between the polymer chains, pushing them apart. This weakens the intermolecular forces so the chains slide more easily and the PVC becomes flexible.