AQA · A-Level · Chemistry
Course version: 7405 · Version from Sept 2016
Structure, bonding and reactivity: Alkenes are unsaturated hydrocarbons.
Alkenes contain only carbon and hydrogen, so they are hydrocarbons, and they contain at least one carbon–carbon double bond, so they are unsaturated.
Checked against the AQA 7405 specification (opens in a new tab) on .
- Point 1 of 2
- 4 key terms
Study notes
From the checked teaching notes for this specification point.
The idea
Alkenes contain only carbon and hydrogen, so they are hydrocarbons, and they contain at least one carbon–carbon double bond, so they are unsaturated. Unsaturated has a precise meaning: the molecule can add extra atoms across that double bond without losing anything, unlike a saturated alkane, which can only substitute. A single double bond gives the general formula CₙH₂ₙ, two hydrogens fewer than the alkane with the same number of carbons. The practical consequence is the test for unsaturation: shaking with bromine water at room temperature turns it from orange to colourless as bromine adds across the double bond, while an alkane leaves it orange. Say colourless, not clear, because the alkane mixture is also clear.
What earns the marks
- Defining unsaturated as containing a carbon–carbon double bond.
- Saying an unsaturated molecule can undergo addition reactions.
- The general formula CₙH₂ₙ for an alkene with one double bond.
- The bromine water observation, orange to colourless, at room temperature.
Common mistakes and how to put them right
Writing that bromine water "goes clear", when the required word is colourless.
Defining unsaturated as containing any double bond, when it must be carbon to carbon.
Giving the general formula as CₙH₂ₙ₊₂, which is the alkane formula.
Saying "decolourises bromine water" without stating the starting colour.
Exam tips
- Give both colours in any observation answer, before and after.
- Count the hydrogens against CₙH₂ₙ to check a structure you have drawn is really an alkene.
- Remember hydrocarbon means carbon and hydrogen only, so a molecule containing oxygen is not an alkene.
Try the lesson
The start of the Structure, bonding and reactivity: Alkenes are unsaturated hydrocarbons. lesson, made from checked teaching notes for this specification point.
Have a go first
Which statement best describes why alkenes are classified as unsaturated hydrocarbons?
Listen
Alkenes contain only carbon and hydrogen, so they are hydrocarbons, and they contain at least one carbon–carbon double bond, so they are unsaturated. Unsaturated has a precise meaning: the molecule can add extra atoms across that double bond without losing anything, unlike a saturated alkane, which can only substitute. A single double bond gives the general formula CₙH₂ₙ, two hydrogens fewer than the alkane with the same number of carbons. The practical consequence is the test for unsaturation: shaking with bromine water at room temperature turns it from orange to colourless as bromine adds across the double bond, while an alkane leaves it orange. Say colourless, not clear, because the alkane mixture is also clear. A strong answer earns marks for these points. defining unsaturated as containing a carbon–carbon double bond. saying an unsaturated molecule can undergo addition reactions. the general formula CₙH₂ₙ for an alkene with one double bond. the bromine water observation, orange to colourless, at room temperature. Exam tip: Give both colours in any observation answer, before and after.
See it
Key words
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unsaturation
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carbon–carbon double bond
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general formula
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test with bromine water
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See every definition
- unsaturation
- Containing a carbon–carbon double bond, so the molecule can add extra atoms across that double bond without losing anything.
- carbon–carbon double bond
- The feature that makes a hydrocarbon unsaturated, allowing it to add extra atoms without losing anything.
- general formula
- For an alkene with one double bond, CₙH₂ₙ, which is two hydrogens fewer than the alkane with the same number of carbons.
- test with bromine water
- Shaking with bromine water at room temperature turns it from orange to colourless as bromine adds across the double bond, while an alkane leaves it orange.
Label the diagram
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