Alkenes
Summary: Alkenes are unsaturated hydrocarbons with C=C double bond (CnH2n). Ethene (C2H4) is the simplest. They undergo addition reactions (bromine, hydrogen, steam) and polymerisation. Tags: igcse chemistry organic-chem Created: 2026-07-14 Last Updated: 2026-07-16
What are Alkenes?
Alkenes are a homologous series of unsaturated hydrocarbons with the general formula:
CnH2n
Unsaturated means the molecule contains at least one carbon-carbon double bond (C=C). The double bond consists of one sigma bond and one pi bond. Because of the double bond, alkenes have two fewer hydrogen atoms than the corresponding alkane.
Alkenes are much more reactive than alkanes because the C=C double bond can open up, allowing atoms to add across it.
The First Three Alkenes
| Name | n | Molecular Formula | Structural Formula | Notes |
|---|---|---|---|---|
| Ethene | 2 | C2H4 | CH2=CH2 | Simplest alkene; plant hormone (ripening) |
| Propene | 3 | C3H6 | CH3CH=CH2 | Used to make poly(propene) |
| Butene | 4 | C4H8 | CH3CH2CH=CH2 (but-1-ene) or CH3CH=CHCH3 (but-2-ene) | Two structural isomers depending on the position of the double bond |
There is no “methene” — the simplest alkene has 2 carbon atoms (ethene) because at least two carbons are needed to form a C=C double bond.
Displayed formulas (showing all atoms and bonds):
- Ethene (C2H4): H2C=CH2 — two carbon atoms joined by a double bond, each carbon bonded to two H atoms
- Propene (C3H6): CH3-CH=CH2 — three carbon chain with a double bond between C1 and C2
- But-1-ene: CH3CH2CH=CH2 — the double bond is between C1 and C2
Test for Unsaturation: Bromine Water Test
This is the distinguishing test between alkanes and alkenes:
| Test | With Alkane | With Alkene |
|---|---|---|
| Add a few drops of bromine water (orange/brown) and shake | Stays orange/brown (no reaction in the dark) | Turns colourless (decolourises immediately) |
Why? The C=C double bond in alkenes undergoes an addition reaction with bromine. The bromine adds across the double bond, forming a colourless dibromoalkane:
C2H4 (g) + Br2 (aq) → CH2BrCH2Br (l)
Ethene + Bromine → 1,2-dibromoethane
Orange/brown Colourless
This reaction happens without UV light — unlike the substitution reaction of alkanes. The double bond is already reactive enough.
Addition Reactions of Alkenes
In all addition reactions, the C=C double bond opens up and atoms add across it. Only one product is formed.
Addition of Hydrogen (Hydrogenation)
Alkene + H2 → Alkane
C2H4 (g) + H2 (g) --(Ni catalyst, 150 °C)--> C2H6 (g)
Ethene + Hydrogen → Ethane
Conditions: Nickel catalyst, 150 °C Use: Converting unsaturated oils to saturated fats (margarine manufacture — making oils solid at room temperature)
Addition of Halogens (Bromination/Chlorination)
Alkene + Halogen → Dihaloalkane
C2H4 (g) + Br2 (aq) → CH2BrCH2Br (l)
Ethene + Bromine → 1,2-dibromoethane
C2H4 (g) + Cl2 (g) → CH2ClCH2Cl (l)
Ethene + Chlorine → 1,2-dichloroethane
No catalyst or UV light required — the reaction is spontaneous.
Addition of Steam (Hydration)
Alkene + H2O (steam) → Alcohol
C2H4 (g) + H2O (g) --(H3PO4 catalyst, 300 °C, 60 atm)--> C2H5OH (l)
Ethene + Steam → Ethanol
Conditions: Phosphoric acid (H3PO4) catalyst, 300 °C, 60 atmospheres pressure Use: Industrial production of ethanol (hydration of ethene)
Addition of Hydrogen Halides
Alkene + Hydrogen halide → Halogenoalkane
C2H4 (g) + HCl (g) → CH3CH2Cl (g)
Ethene + Hydrogen chloride → Chloroethane
C2H4 (g) + HBr (g) → CH3CH2Br (l)
Ethene + Hydrogen bromide → Bromoethane
No catalyst or UV light required.
Addition Polymerisation
Polymerisation is the process in which many small monomer molecules (alkenes) join together to form a very large polymer molecule.
Key points:
- The monomers are small alkene molecules (e.g., ethene)
- The C=C double bond in each monomer opens up
- Monomers join by single covalent bonds to form a long chain
- The polymer is saturated (contains only C-C single bonds in the main chain)
- No other products are formed — this is an addition polymerisation
Common Addition Polymers
| Monomer | Monomer Structure | Polymer Name | Repeating Unit | Uses |
|---|---|---|---|---|
| Ethene | CH2=CH2 | Poly(ethene) or polythene | -(CH2-CH2)- | Plastic bags, bottles, cling film |
| Propene | CH3CH=CH2 | Poly(propene) | -(CH(CH3)-CH2)- | Ropes, carpets, syringes, food containers |
| Chloroethene (vinyl chloride) | CH2=CHCl | Poly(chloroethene) / PVC | -(CH2-CHCl)- | Drainpipes, window frames, electrical insulation |
| Tetrafluoroethene | CF2=CF2 | Poly(tetrafluoroethene) / PTFE (Teflon) | -(CF2-CF2)- | Non-stick cookware, waterproof coatings |
Drawing the polymer repeating unit from a monomer:
Example: Poly(ethene) from ethene
- Monomer: CH2=CH2
- Open the double bond: -CH2-CH2-
- Repeating unit: -(CH2-CH2)-
Example: Poly(propene) from propene
- Monomer: CH3CH=CH2
- Open the double bond: -(CH(CH3)-CH2)-
- The -CH3 group is a side branch, not part of the main chain
When drawing repeating units, show the open bonds extending through the brackets (one on each side) to indicate the chain continues.
Distinguishing Alkanes from Alkenes
| Property | Alkanes | Alkenes |
|---|---|---|
| General formula | CnH2n+2 | CnH2n |
| Bonding | Only C-C single bonds (saturated) | At least one C=C double bond (unsaturated) |
| Bromine water test | Stays orange/brown (no reaction without UV) | Turns colourless immediately |
| Type of reaction | Substitution (with halogens, UV light) | Addition |
| Polymerisation | Does NOT undergo addition polymerisation | Undergoes addition polymerisation |
Key Points
- General formula: CnH2n
- Alkenes are unsaturated (contain C=C double bond)
- First three: ethene (C2H4), propene (C3H6), butene (C4H8)
- Bromine water test: orange/brown → colourless with alkenes (addition); stays orange with alkanes
- Hydrogenation: alkene + H2 → alkane (Ni catalyst, 150 °C)
- Hydration: alkene + H2O → alcohol (H3PO4, 300 °C, 60 atm)
- Bromination: alkene + Br2 → dibromoalkane (no catalyst needed)
- Addition polymerisation: many monomers join via opening of C=C bonds to form a long saturated chain
- Common polymers: poly(ethene), poly(propene), PVC, PTFE
Key Concepts from Past Papers
- Fractional distillation depends on boiling point
- Petroleum is heated and vaporised; vapour enters at bottom of fractionating column
- Bromine water test: alkanes stay orange, alkenes decolourise
Keywords from Past Papers
methane, ethene, point, bonds, carbon, fractions, alkenes, energy, hydrocarbons, boiling, idea, structure, water, alcohol, addition
Related Notes
Sources
- OpenStax Chemistry 2e — [Chapter 20: Organic Chemistry (Alkenes)], Rice University (free, CC BY 4.0)
- BBC Bitesize GCSE Chemistry — [Alkenes], BBC (free educational resource)
- Cambridge IGCSE Chemistry 0620 — Syllabus Section 11: Organic Chemistry (Alkenes), Cambridge Assessment International Education
- CK-12 Chemistry for High School — [Chapter 25: Alkenes], CK-12 Foundation (free, CC BY-NC 3.0)
Past Paper Sources
- 0620/32 Feb/March 2017: Q33(b)(iv) (1m), Q33(c)(iii) (1m)
- 0620/32 Feb/March 2018: Q66(a)(i) (1m)
- 0620/32 Feb/March 2019: Q55(d)(iii) (1m)
- 0620/32 Feb/March 2020: Q11(a)(ii) (1m), Q11(a)(v) (1m)
- 0620/32 Feb/March 2021: Q66(c)(i) (1m)
- 0620/32 Feb/March 2022: Q22(a)(ii) (2m), Q77(b)(i) (1m)
- 0620/32 Feb/March 2023: Q66(a)(ii) (1m), Q66(a)(iv) (2m)
- 0620/32 May/June 2018: Q11(a)(v) (1m), Q33(a)(iv) (1m), Q33(c)(ii) (0m) (+1 more)
- 0620/33 May/June 2016: Q44(c)(iv) (1m), Q66(e)(i) (1m)
- 0620/33 May/June 2017: Q44(a)(ii) (1m)
- 0620/33 May/June 2019: Q11(a)(i) (2m), Q11(a)(iv) (1m), Q11(a)(vi) (1m) (+3 more)
- 0620/33 May/June 2021: Q44(a)(iii) (1m), Q44(d)(i) (1m), Q44(d)(ii) (1m) (+1 more)
Common Misconceptions
| Misconception | Reality |
|---|---|
| ”Alkanes and alkenes both decolourise bromine water” | Only alkenes decolourise bromine water. Alkanes do NOT react with bromine without UV light |
| ”There is a methene with one carbon” | The simplest alkene is ethene (C2H4). At least two carbon atoms are needed for a C=C double bond — there is no CH2 molecule |
| ”Alkenes undergo substitution like alkanes” | Alkenes undergo addition, not substitution. The C=C double bond opens and atoms add across it |
| ”The polymer still has C=C double bonds” | The polymer chain is saturated — all C=C bonds in the monomers have opened and formed single bonds. The polymer has only C-C single bonds |
| ”Addition and substitution both need UV light” | Addition reactions of alkenes are spontaneous (no UV needed). Only alkane substitution requires UV light |
| ”Polymerisation is a condensation reaction” | Addition polymerisation produces only the polymer — no small molecules (like water) are eliminated. Condensation polymerisation is different |