Syllabus Edition

First teaching 2023

First exams 2025

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IUPAC Nomenclature (HL IB Chemistry)

Revision Note

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Richard

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Chemistry

IUPAC Nomenclature

  • IUPAC or systematic nomenclature can be used to name organic compounds and therefore make it easier to refer to them

Naming hydrocarbons

  • Hydrocarbons are compounds containing hydrogen and carbon only
  • There are four families of hydrocarbons you should know: 
    1. Alkanes
    2. Alkenes
    3. Alkynes
    4. Arenes

Naming alkanes

  • Alkanes have the general molecular formula CnH2n+2
    • They contain only single bonds and are said to be saturated
  • Alkanes are named using the nomenclature rule alk + ane
    • The alk depends on the number of carbons as outlined in the following table 
  • The alkanes provide the basis of the naming system and the stem of each name indicates how many carbon atoms are in the longest chain in one molecule of the compound

IUPAC system of naming alkanes table

Number of carbon atoms Molecular formula of straight-chain alkane IUPAC name of alkane Stem used in naming
1 CH4 methane meth-
2 C2H6 ethane eth-
3 C3H8 propane prop-
4 C4H10 butane but-
5 C5H12 pentane pent-
6 C6H14 hexane hex-
7 C7H16 heptane hept-
8 C8H18 octane oct-
9 C9H20 nonane non-
10 C10H22 decane dec-

Exam Tip

Although the table shows up to 10 carbons for reference, in your IB Chemistry exam you are only required to name molecules with up to 6 carbons

  • If there are any side-chains or functional groups present, then the position of these groups is indicated by numbering the carbon atoms in the longest chain starting at the end that gives the lowest possible numbers in the name
  • The hydrocarbon side chain is shown in brackets in the structural formula

CH3CH(CH3)CH2CH3

  • The side-chain is named by adding ‘-yl’ to the normal alkane stem
  • This type of group is called an alkyl group

Naming organic compounds with one alkyl side chain

Diagram showing that the longest chain is 6 carbons and there is a methyl group on carbon-3, so it is 3-methylhexane

The longest chain provides the main name and the side chain is shown as a numbered alkyl prefix

  • If there are more than one of the same alkyl side chain or functional groups, di- (for two), tri- (for three) or tetra- (for four) is added in front of its name
  • The adjacent numbers have a comma between them
  • Numbers are separated from words by a hyphen

Naming organic compounds with multiple, identical side chains

3,3,4-trimethylhexane - the longest chain is 6 carbons and there are 3 methyl groups on carbons 3, 3 and 4

The longest chain still provides the main name and the side chains are shown as numbered alkyl prefixes

  • If there is more than one type of alkyl side chain, the same numbering system applies but the different side chains are listed in alphabetic order

Naming organic compounds with multiple, different side chains

4-ethyl-2-methylhexane - the longest chain is 6 carbons with 1 ethyl group on carbon-4 and 1 methyl group on carbon-2

The longest chain still provides the main name and the side chains are still shown as numbered alkyl prefixes but in alphabetical order

Naming alkenes

  • Alkenes have the general molecular formula CnH2n
  • They are said to be unsaturated
  • Alkenes are named using the nomenclature rule alk + ene
  • In molecules with a straight chain of 4 or more carbon atoms, the position of the C=C double bond must be specified
    • The carbon atoms on the straight chain must be numbered, starting with the end closest to the double bond
    • The lowest-numbered carbon atom participating in the double bond is indicated just before the -ene:

IUPAC system of naming alkenes table

Number of carbon atoms Displayed formula of straight-chain alkene Molecular formula of alkene IUPAC name of alkene
1 - - -
2 ethene-displayed C2H4 ethene
3 propene-displayed C3H6 propene
4 but-1-ene-displayed C4H8 but-1-ene
5 pent-2-ene-displayed C5H10 pent-2-ene
6 hex-3-ene-displayed C6H12 hex-3-ene

 

  • There is a distinction to be made between the name of the functional group and the name of the family
    • The name of the family is alkene
    • The name of the functional group is alkenyl

Naming alkynes

  • Alkynes have the general molecular formula CnH2n-2
  • The triple bond makes them unsaturated molecules
  • Alkenes are named using the nomenclature rule alk + yne
  • In molecules with a straight chain of 4 or more carbon atoms, the position of the C=C triple bond must be specified
    • The carbon atoms on the straight chain must be numbered, starting with the end closest to the triple bond
    • The lowest-numbered carbon atom participating in the triple bond is indicated just before the -yne:

IUPAC system of naming alkynes table

Number of carbon atoms Displayed formula of straight-chain alkyne Molecular formula of alkyne IUPAC name of alkyne
1 - - -
2 ethyne-displayed C2H2 ethyne
3 propyne-displayed C3H4 propyne
4 but-1-yne-displayed C4H6 but-1-yne
5 pent-2-yne-displayed C5H8 pent-2-yne
6 hex-3-yne-displayed C6H10 hex-3-yne

 

  • There is a distinction to be made between the name of the functional group and the name of the family
    • The name of the family is alkyne
    • The name of the functional group is alkynyl

Naming arenes

  • Arenes are aromatic compounds, i.e. compounds with one or more rings with pi electrons that are delocalised throughout the ring(s)

  • Benzene, C6H6, is the only aromatic hydrocarbon that is covered in IB Chemistry and is covered in our Benzene revision note
  • Naming aromatic compounds depends on whether the benzene ring is considered the main structure or a functional group
    • Benzene as the main structure:
      • Alkyl groups attached to benzene rings are named using the nomenclature rule alkyl group + benzene
      • If there is only one alkyl group attached, then no numbering system is applied to the benzene ring
      • If more than one alkyl group is attached, then a relative numbering system is applied
        • This is where the longest alkyl chain is considered as being attached to carbon-1 of the ring
        • The other alkyl groups are then numbered accordingly 
        • The alkyl groups are still named in alphabetical order 

Examples of alkyl substituted aromatic compounds

Skeletal structures of methylbenzene and 1-ethyl-2-methylbenzene

Methylbenzene is often called by the common name toluene. 1-ethyl-2-methylbenzene has the longest (ethyl) side chain set as carbon-1, so the methyl side chain is attached to carbon-2

    • Benzene as a functional group:
      • The functional group in benzene is known as a phenyl group when attached to other molecules

Benzene as the functional group

Skeletal structure of phenylamine

The benzene ring is considered a functional group in amine structures, which means that this aromatic compound is called phenylamine

Halogenoalkanes

  • Halogenoalkanes have the general molecular formula, CnH2n+1X, where X represents a halogen
  • Halogenoalkanes are named using the prefix chloro-, bromo- or iodo-, with the ending -ane
  • In molecules with a straight chain of three or more carbon atoms, the position of the halogen atom must also be specified
    • The carbon atoms on the straight chain must be numbered, starting with the end closest to the halogen atom
    • The number of the carbon atom attached to the halogen is indicated before the prefix:

Halogenoalkanes Examples Table

Displayed formula of halogenoalkane Molecular formula of halogenoalkane IUPAC name of halogenoalkane
chloroethane-displayed-formula C2H5Cl chloroethane
2-bromopropane-displayed-formula C3H7Br 2-bromopropane
1-iodopentane-displayed-formula C5H11I 1-iodopentane
3-chloropentane-displayed-formul C5H11Cl 3-chloropentane

 

  • For halogenoalkanes with multiple halogen functional groups, the position and type of functional group must be given
    • For example, an ethane chain with 2 chlorine functional groups on carbon-1 and one chlorine functional group on carbon 2 will be named 1,1,2-trichloroethane

Alcohols

  • Alcohols are a family of molecules that contain the hydroxyl functional group, -OH
  • Their general formula is  CnH2n+1OH
  • The nomenclature of alcohols follows the pattern alkan + ol
    • If there are two -OH groups present the molecule is called a diol

Primary alcohols examples table

Displayed formula of primary alcohol Structural formula of primary alcohol IUPAC name of primary alcohol
methanol-displayed-formula CH3OH methanol
ethanol-displayed-formula CH3CH2OH ethanol
propan-1-ol-displayed-formula CH3CH2CH2OH propan-1-ol
butan-1-ol-displayed-formula CH3CH2CH2CH2OH butan-1-ol

 

Carbonyls

  • Carbonyl is the collective name for compounds containing the functional group C=O
  • The general formula of a carbonyl is CnH2nO
  • The two sub-families of carbonyls are aldehydes and ketones (known in some countries as alkanals and alkanones)

Aldehydes

  • If the carbonyl group is on the end of a chain then it is an aldehyde and has the functional group formula, RCHO
    • The H is written before the O so as not to confuse it with an alcohol
  • The nomenclature of carbonyls follows the pattern alkan + al
  • There is no need to use numbers in the name as aldehyde will always be on the number 1 carbon atom

Ketones

  • Ketones have a minimum of three carbons and have the general functional group formula, RCOR
  • The nomenclature of ketones follows the pattern alkan + one
  • After butanone, the carbonyl group can have positional isomers, so numbering must be used
    • For example pentan-2-one and pentan-3-one

Carbonyls examples table

Displayed formula of carbonyl Structural formula of carbonyl IUPAC name of carbonyl
methanal-displayed-formula CH2O methanal (also known as formaldehyde)
ethanal-displayed-formula CH3CHO ethanal
propanone-displayed-formula CH3COCH3 propanone (also known as acetone)
butanone-displayed-formula CH3CH2COCH3 butanone
     
  • As they have a very similar functional group arrangement, aldehydes and ketones show similar chemical reactions
  • Differences in their chemistry are due to the reactions that involve the H on the aldehyde or the nature of the R group
  • The difference in electronegativity between oxygen and carbon means the C=O is polar, leading to dipole-dipole attractions between the molecules which results in:
    • Higher than expected boiling points for small molecules
    • Solubility in water for the lower members of the families
  • Aldehydes and ketones with the same number of carbons are functional group isomers

Carboxylic acids

  • Carboxylic acid is the name given to compounds containing the functional group carboxyl, -COOH
  • The general formula of a carboxylic acid is CnH2n+1COOH which can be shortened to just RCOOH
    • (In some countries the family is  called alkanoic acid)
  • The nomenclature of carboxylic acids follows the pattern alkan + oic acid
  • There is no need to use numbers in the name as the carboxyl group will always be on the number 1 carbon atom

Carboxylic Acids Examples Table

Displayed formula of carboxylic acid Structural formula of carboxylic acid IUPAC name of carboxylic acid
methanoic-acid-displayed-formula HCO2H methanoic acid (also known as formic acid) 
ethanoic-acid-displayed-formula CH3CO2H ethanoic acid (also known as acetic acid)
propanoic-acid-displayed-formula CH3CH2CO2H propanoic acid

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Richard

Author: Richard

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.