Reactions of Alkenes (SQA National 5 Chemistry): Revision Note

Exam code: X813 75

Richard Boole

Written by: Richard Boole

Reviewed by: Philippa Platt

Updated on

Addition reactions of alkenes

  • Alkenes undergo addition reactions

    • This is where the double bond breaks open and the atoms of another molecule are "added across" it

  • In an addition reaction:

    • The C=C double bond becomes a C-C single bond

    • The product is always a saturated compound

    • Only one product is formed

  • There are several important types of addition reactions

  • The three most common involve adding small molecules like:

    • Hydrogen, H2

    • Halogens, e.g. Cl2, Br2

    • Water, H2O

1. Addition of hydrogen

  • This reaction is:

alkene + hydrogen → alkane

  • The process: Adding hydrogen to an alkene is called hydrogenation

    • The hydrogen atoms "add across" the double bond

    • This turns the unsaturated alkene into a saturated alkane

  • Conditions: This reaction requires a nickel catalyst and heat

Example hydrogenation reaction

ethene + hydrogen → ethane

C2H4 + H2 → C2H6

The addition / hydrogenation reaction between ethene and hydrogen to form ethane.
In hydrogenation, a hydrogen molecule adds across the double bond of an alkene to form an alkane

2. Addition of halogens

  • This reaction is:

alkene + halogen → dihaloalkane

  • The process: Adding a halogen to an alkene is called halogenation

    • The halogen atoms "add across" the double bond

    • This turns the unsaturated alkene into a saturated dihaloalkane

      • A dihaloalkane is an alkane molecule that has two halogen atoms attached to it

  • There are specific types of halogenation reaction:

    • Chlorination is the addition of chlorine, Cl2

    • Bromination is the addition of bromine, Br2

      • The addition of bromine to an alkene is the standard

Example halogenation reaction

ethene + bromine → 1,2-dibromoethane

C2H4 + Br2 → C2H4Br2

  • This is the reaction that happens in the test for unsaturation, where the orange-brown bromine solution is decolourised

The halogenation reaction between ethene and bromine forming 1,2-dibromoethane.
A bromine molecule adds across the double bond, decolourising the bromine solution and forming a dihaloalkane

Examiner Tips and Tricks

You are not required to name the dihaloalkane product of a halogenation reaction as part of this course.

3. Addition of water (steam)

  • This reaction is:

alkene + water (steam) → alcohol

  • The process: Adding water to an alkene is called hydration

    • The water "adds across" the double bond

    • This turns the unsaturated alkene into an alcohol

  • Hydration is a key industrial method for making alcohols

  • Conditions: This reaction requires:

    • High temperature

    • High pressure

    • An acid catalyst, such as phosphoric acid

Example hydration reaction

ethene + water (steam) → ethanol

C2H4 + H2O → C2H5OH

The hydration reaction between ethene and steam to form ethanol, with reaction conditions labelled.
In hydration, a water molecule adds across the double bond of an alkene to form an alcohol

Examiner Tips and Tricks

To draw the product of any addition reaction:

  1. Redraw the alkene

    1. But, change the C=C double bond to a C-C single bond

  2. This gives the two carbon atoms "spare" bonds

  3. "Add" the atoms from the other molecule to these two spare bonds:

    1. For hydrogenation, add H and H

    2. For halogenation with bromine, add Br and Br

    3. For hydration, add H to one bond and OH to the other bond

A special type of addition: Polymerisation

  • Addition reactions can also happen between many alkene molecules themselves

  • This process is called addition polymerisation, which is how plastics are made

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Richard Boole

Author: Richard Boole

Expertise: Chemistry Content Creator

Richard has taught Chemistry for over 15 years as well as working as a science tutor, examiner, content creator and author. He wasn’t the greatest at exams and only discovered how to revise in his final year at university. That knowledge made him want to help students learn how to revise, challenge them to think about what they actually know and hopefully succeed; so here he is, happily, at SME.

Philippa Platt

Reviewer: Philippa Platt

Expertise: Chemistry Content Creator

Philippa has worked as a GCSE and A level chemistry teacher and tutor for over thirteen years. She studied chemistry and sport science at Loughborough University graduating in 2007 having also completed her PGCE in science. Throughout her time as a teacher she was incharge of a boarding house for five years and coached many teams in a variety of sports. When not producing resources with the chemistry team, Philippa enjoys being active outside with her young family and is a very keen gardener