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3.2.4Additional lessons

IUPAC Nomenclature — IB Chemistry SL Revision Notes & Topical Questions

5 min read 6 parts Lesson 46 of 98

📚 IB Chemistry SL Hub / Topical Revision
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Part 1 of 6Building a Name

3.2.4 IUPAC Nomenclature

A systematic name is assembled in a fixed order so that every compound has one unambiguous name.

1
Find the longest continuous carbon chain that contains the principal functional group; its length gives the stem: meth, eth, prop, but, pent or hex.
2
Identify the suffix set by the highest-priority functional group, such as -ane, -ene, -ol, -al, -one, -oic acid or -amine.
3
Number the chain from the end that gives the principal functional group the lowest possible number.
4
Name each branch as an alkyl group (methyl, ethyl, propyl) or a halogen prefix (chloro, bromo) and give it the number of the carbon carrying it.
5
Arrange the prefixes alphabetically, use di, tri or tetra for repeats, and separate numbers with commas and numbers from words with hyphens.

Part 2 of 6Stems and Suffixes

Alkane stem
  • Counting carbons gives meth (1), eth (2), prop (3), but (4), pent (5) and hex (6), with -ane for single bonds only.
Alkene and alkyne
  • A C=C bond gives the ending -ene and a C≡C bond gives -yne, with a number showing where the multiple bond starts.
Alcohol
  • The –OH group is shown by the ending -ol, as in propan-2-ol, where the number locates the carbon bearing the hydroxyl.
Aldehyde and ketone
  • An aldehyde ends in -al and is always carbon 1, whereas a ketone ends in -one and needs a number when the chain is long enough.
Acid and amine
  • A carboxylic acid ends in -oic acid with the acid carbon as carbon 1, and a primary amine ends in -amine.
GroupSuffix or prefixExample
Alkane-anebutane
Alkene-enebut-1-ene
Alcohol-olpentan-2-ol
Aldehyde-alpropanal
Ketone-onebutanone
Carboxylic acid-oic acidethanoic acid
Halogenoalkanechloro-, bromo-2-chloropropane
Amine-amineethanamine

Part 3 of 6Branches and Numbering

Branches and Numbering
Alkyl branches
  • A branch that is a carbon chain missing one hydrogen is named from its stem with -yl, for example CH₃ is methyl and C₂H₅ is ethyl.
Lowest locants
  • When a name has several substituents, choose the numbering direction that gives the smaller number at the first point of difference.
Repeated groups
  • Identical branches are counted with di, tri or tetra, and each one still needs its own locant, as in 2,2-dimethylbutane.
Alphabetical order
  • Prefixes are listed alphabetically ignoring di and tri, so ethyl comes before methyl in 3-ethyl-2-methylpentane.

Part 4 of 6Reading a Name Backwards

1
Start with the stem and suffix to draw the main chain and put the functional group in place, for example hex-2-ene has six carbons with a double bond between C2 and C3.
2
Add each branch at its stated position, remembering that locants refer to the numbered carbons of the main chain.
3
Fill the remaining bonds of every carbon with hydrogen atoms so each carbon has four bonds in total.
4
Check the name you would give your drawing; if it differs from the original, a longest chain or a numbering step has gone wrong.

Part 5 of 6Worked Example

Question Name the compound CH₃CH(CH₃)CH₂CH(OH)CH₃.

  1. The longest chain containing the carbon bearing OH has five carbons, so the stem is pentane and the group is an alcohol (-ol).
  2. Number from the end nearer the OH group: counting from the right-hand CH₃ the OH carbon is C2, whereas counting from the left it would be C4.
  3. With this numbering the methyl branch sits on C4, so the substituent is 4-methyl.
  4. Combine the parts in orderbranch prefix, stem, locant and suffix.

Answer 4-methylpentan-2-ol

Part 6 of 6Exam Checklist & Tips

3.2.4 – Key Points for the Exam

  • Longest chain
    • The longest unbranched carbon chain containing the principal functional group;
      • it sets the stem of the name.
  • Locant A number showing which carbon of the main chain carries a substituent or functional group.
  • Substituent An atom or group attached to the main chain in place of a hydrogen, such as methyl or chloro.
  • Homologous series A family of compounds with the same functional group and general formula, differing by CH₂.
  • Principal functional group The group of highest priority, which determines the suffix and the direction of numbering.

Common Mistakes

  • Choosing the longest visible straight line instead of the longest continuous chain, which may bend around corners in a drawing.
  • Numbering from the wrong end so that the functional group does not receive the lowest number.
  • Listing prefixes by size or number of carbons instead of alphabetically.
  • Omitting commas between locants or writing a number next to a word without a hyphen.

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