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2.5.10Chemical Bonding, Application Of Chemical Reactions and Organic Chemistry

Naming Alkanes and Alkenes

5 min read 7 parts Lesson 50 of 54 1 quiz

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Section 1 of 7Alkanes: saturated hydrocarbons

alkane chain types
alkane chain types
General formula
  • General formula Alkanes have the general formula CnH2n+2. With 5 carbons the formula is C5H12.
Saturated
  • Saturated Every carbon atom forms four bonds, and all the carbon-carbon bonds are single.
    • A compound with only single bonds is saturated.
Properties
  • Properties Alkanes are colourless and fairly unreactive.
    • They burn in combustion reactions and can be cracked into smaller molecules.
  • Physical properties change gradually as the chain gets longer.

Section 2 of 7Alkenes: unsaturated hydrocarbons

alkene general substituents
alkene general substituents
General formula
  • General formula Alkenes have the general formula CnH2n. With 4 carbons the formula is C4H8.
Unsaturated
  • Unsaturated Alkenes contain at least one carbon-carbon double bond, C=C, in addition to single bonds.
    • This is their functional group.
Reactivity
  • Reactivity The double bond makes alkenes more reactive.
    • They burn, take part in addition reactions, and join together in addition polymerisation to make plastics.
  • The smallest alkene has 2 carbons, since a double bond needs two carbon atoms.

Section 3 of 7The naming pattern

Graph of CO2 and methane concentrations from 1000 to 2000
CarbonsPrefixAlkane (formula)Alkene (formula)
1meth-methane, CH4none
2eth-ethane, C2H6ethene, C2H4
3prop-propane, C3H8propene, C3H6
4but-butane, C4H10but-1-ene, C4H8
5pent-pentane, C5H12pent-1-ene, C5H10
6hex-hexane, C6H14hex-1-ene, C6H12

Section 4 of 7Naming branched molecules (HT only)

branched polyene carbon skeleton
branched polyene carbon skeleton
1
Find the longest continuous carbon chain (for an alkene it must include the C=C). This chain gives the stem: meth, eth, prop, but, pent or hex.
2
Decide the ending: -ane if every bond is single, or -ene if there is a double bond, with the position of the double bond given as a number such as but-1-ene.
3
Identify each side-chain: a methyl group, −CH3, or an ethyl group, −C2H5.
4
Number the main chain from the end that gives the lowest numbers, and state which carbon the side-chain is on.
5
Write the name as side-chain position + side-chain + main chain, for example 3-methylpentane or 2-methylbut-1-ene.

Section 5 of 7Worked examples (HT only)

Branched names
2-methylpropane
  • 2-methylpropane The longest chain is 3 carbons (propane) with a methyl group on carbon 2.
    • The number 2 is not strictly needed because a methyl could only sit on the middle carbon.
2-methylbutane
  • 2-methylbutane The longest chain is 4 carbons with a methyl on a middle carbon, which is numbered 2 to get the lowest number.
3-ethylpentane
  • 3-ethylpentane A 5-carbon chain with an ethyl group on the middle carbon.
2-methylbut-1-ene
  • 2-methylbut-1-ene A 4-carbon chain with the double bond starting at carbon 1 and a methyl on carbon 2.
    • Beware that some molecules are drawn 'backwards' so carbon 1 may be on the right.

Section 6 of 7Key terms

TermMeaning
AlkaneA saturated hydrocarbon with only single bonds, general formula CnH2n+2.
AlkeneAn unsaturated hydrocarbon containing a C=C double bond, general formula CnH2n.
SaturatedContaining only single carbon-carbon bonds.
Functional groupThe atom or group of atoms that gives a family of compounds its characteristic reactions.
Side-chainA group such as methyl or ethyl attached to the main carbon chain.

Section 7 of 7Exam technique

1
Choosing a chain that is not the longest. A molecule drawn as a propane chain with an ethyl branch is really a butane with a methyl branch.
2
Saying that an alkene is 'unsaturated because it has no hydrogen'. It is unsaturated because it has a C=C bond.
3
Trying to name a one-carbon alkene. A double bond needs at least two carbon atoms, so ethene is the first.
4
Numbering from the wrong end of the chain; always give the side-chain or double bond the lowest possible number.
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