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This lesson covers alkenes — unsaturated hydrocarbons with a C=C double bond — and their key reactions, as required by the Edexcel GCSE Chemistry specification (1CH0). You need to know the general formula, the first three members, how to test for unsaturation, and the important addition reactions (hydrogenation and hydration).
Alkenes are a homologous series of hydrocarbons that contain at least one carbon–carbon double bond (C=C). Because they have a double bond, they have fewer hydrogen atoms than the equivalent alkane and are described as unsaturated.
| Feature | Detail |
|---|---|
| General formula | CₙH₂ₙ |
| Bonding | Contains a C=C double bond |
| Saturation | Unsaturated (not all carbon atoms are bonded to the maximum number of hydrogen atoms) |
| Reactivity | More reactive than alkanes because of the double bond |
| Property | Alkanes | Alkenes |
|---|---|---|
| General formula | CₙH₂ₙ₊₂ | CₙH₂ₙ |
| Bonding | Single C–C bonds only | Contains a C=C double bond |
| Saturation | Saturated | Unsaturated |
| Reactivity | Relatively unreactive | More reactive (undergo addition reactions) |
| Name | Molecular formula | Number of C atoms | Displayed formula description |
|---|---|---|---|
| Ethene | C₂H₄ | 2 | H₂C=CH₂ — two carbon atoms joined by a double bond, each with two hydrogen atoms |
| Propene | C₃H₆ | 3 | CH₃–CH=CH₂ — three carbon chain with the double bond between C-2 and C-3 |
| Butene | C₄H₈ | 4 | CH₃–CH₂–CH=CH₂ — four carbon chain with the double bond between C-3 and C-4 (but-1-ene) |
Exam Tip: Notice that there is no "methene" — you need at least two carbon atoms to form a C=C double bond. The simplest alkene is ethene.
When drawing the displayed formula of an alkene:
The test to distinguish between alkanes (saturated) and alkenes (unsaturated) uses bromine water.
| Hydrocarbon | Observation | Conclusion |
|---|---|---|
| Alkene (unsaturated) | Bromine water changes from orange/brown to colourless (decolourises) | The C=C double bond reacts with bromine — addition reaction occurs |
| Alkane (saturated) | Bromine water stays orange/brown (no colour change) | No double bond to react with — no addition reaction |
Exam Tip: The key phrase is "bromine water is decolourised" (not "turns clear"). Colourless and clear are different things in chemistry — a coloured solution can still be clear. Always say decolourised.
Alkenes are more reactive than alkanes because the C=C double bond can open up, allowing atoms to add across the double bond. This type of reaction is called an addition reaction.
In an addition reaction:
Hydrogenation is the addition of hydrogen (H₂) across the double bond of an alkene to form an alkane.
Word equation: ethene + hydrogen → ethane
Symbol equation: C₂H₄ + H₂ → C₂H₆
Hydrogenation is used industrially to convert vegetable oils (which contain C=C double bonds) into solid fats for making margarine and other spreads. The process hardens the oil by converting unsaturated fats into saturated fats.
| Before hydrogenation | After hydrogenation |
|---|---|
| Liquid vegetable oil (unsaturated) | Solid/semi-solid fat (saturated) |
| Contains C=C double bonds | C=C bonds converted to C–C single bonds |
Hydration is the addition of water (as steam) across the double bond of an alkene to produce an alcohol.
Word equation: ethene + steam → ethanol
Symbol equation: C₂H₄ + H₂O → C₂H₅OH
This is the industrial method for producing ethanol (the alcohol found in alcoholic drinks and used as a solvent and fuel). Ethanol produced this way is sometimes called synthetic ethanol because it is made from a petrochemical feedstock (ethene) rather than from fermentation.
Exam Tip: Make sure you can recall the catalyst for each reaction: nickel for hydrogenation and phosphoric acid for hydration. These are commonly tested.
The reaction of an alkene with bromine is also an addition reaction (this is the basis of the bromine water test):
Word equation: ethene + bromine → dibromoethane
Symbol equation: C₂H₄ + Br₂ → C₂H₄Br₂
The product, 1,2-dibromoethane, is colourless, which is why the orange bromine water is decolourised.
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