IUPAC Rules
A concise revision guide to the key IUPAC naming rules used in A Level organic chemistry, including formula types, displayed formulae, skeletal formulae, carbon chain prefixes, functional group naming and numbering rules.
- 3.3.1.1i-a
- 3.3.1.1i-b
- 3.3.1.1i-c
- 3.3.1.1i-d
- 3.3.1.1i-e
- 3.3.1.1i-f
- 3.3.1.1ii-b
- 3.3.1.1ii-c
- 3.3.1.1iii
- 3.3.1.1iv-a
What these spec points say
- 3.3.1.1i-a know that organic compounds can be represented by empirical formula
- 3.3.1.1i-b know that organic compounds can be represented by molecular formula
- 3.3.1.1i-c know that organic compounds can be represented by general formula
- 3.3.1.1i-d know that organic compounds can be represented by structural formula
- 3.3.1.1i-e know that organic compounds can be represented by displayed formula
- 3.3.1.1i-f know that organic compounds can be represented by skeletal formula
- 3.3.1.1ii-b draw displayed formulas for given organic compounds
- 3.3.1.1ii-c draw skeletal formulas for given organic compounds
- 3.3.1.1iii know the characteristics of a homologous series as a series of compounds containing the same functional group
- 3.3.1.1iv-a apply IUPAC rules for nomenclature to name organic compounds with chains up to six carbon atoms
Tetrahedral Carbon and the Zig-Zag Chain
Choose a step to watch four bonding pairs spread to 109.5° and then build, twist and flatten a butane chain. Drag to rotate.
© Dr. Mohammed Al-Fatah – onlinelearningsystem.net
GCSE Recap: Bonds in a Displayed Formula
Before you start, check that you remember how many bonds each kind of atom forms and what makes a compound a hydrocarbon.
Key Organic Chemistry Definitions
Before naming organic compounds, you need to recognise the basic language used to describe formulae, bonding and families of compounds.
Hydrocarbon
A compound consisting of hydrogen and carbon only.
Saturated
A compound containing single carbon-carbon bonds only.
Unsaturated
A compound containing at least one C=C double bond.
Molecular formula
The formula showing the actual number of each type of atom in a molecule.
Empirical formula
The simplest whole number ratio of atoms of each element in a compound.
General formula
An algebraic formula for a homologous series, such as CnH2n for alkenes.
Structural formula
The minimal detail needed to show the arrangement of atoms in a molecule, such as CH3CH2CH2CH3.
Displayed formula
A formula showing all covalent bonds present in a molecule.
Key idea: IUPAC naming depends on identifying the carbon skeleton, the functional group and the correct numbering system.
Quick Check: Which Kind of Formula?
Decide quickly which term describes each formula or compound.
Empirical and Molecular Formulae in Organic Chemistry
The specification lists the empirical formula alongside the molecular, general, structural, displayed and skeletal formulae as ways of representing an organic compound.
The empirical formula is the simplest whole-number ratio of the atoms of each element; the molecular formula gives the actual number of atoms of each element in one molecule.
For organic compounds the two are often different, because carbon chains repeat the same CH2 unit.
| Compound | Molecular formula | Empirical formula | Comment |
|---|---|---|---|
| Ethane | C2H6 | CH3 | Divide both numbers by 2 |
| Butene | C4H8 | CH2 | Every alkene with one C=C bond and no ring has the empirical formula CH2 |
| Ethanoic acid | C2H4O2 | CH2O | Shares its empirical formula with methanal, CH2O, and glucose, C6H12O6 |
| Methane | CH4 | CH4 | Already the simplest ratio, so the two formulae are the same |
Finding the empirical formula from composition
A compound contains 40.0% carbon, 6.7% hydrogen and 53.3% oxygen by mass.
Divide each percentage by the relative atomic mass to get the mole ratio: C (40.0) / (12.0) = 3.33, H (6.7) / (1.0) = 6.7, O (53.3) / (16.0) = 3.33.
Dividing by the smallest value gives C 1 : H 2 : O 1, so the empirical formula is CH2O.
Scaling up to the molecular formula
The empirical formula mass of CH₂O is 30.0. If the compound has a relative molecular mass of 60.0, then (60.0) / (30.0) = 2 and the molecular formula is C₂H₄O₂, which could be ethanoic acid.
If the relative molecular mass were 30.0 the compound would be methanal, CH₂O.
The empirical formula alone never identifies an organic compound. You need the relative molecular mass, usually from a mass spectrum, and then the structural formula to decide which isomer it is.
Exam focus: Show every step: percentages to moles, divide by the smallest, multiply to whole numbers, then compare the empirical formula mass with Mr. State clearly which formula is empirical and which is molecular.
Quick Check: Empirical and Molecular Formulae
Complete the comparison of two six-carbon hydrocarbons.
Quick Check: From Percentages to Molecular Formula
Work out the molecular formula on paper, then choose your answer.
Displayed and Skeletal Formulae
When drawing organic compounds, add hydrogen atoms so that each carbon forms four bonds. In saturated hydrocarbons, the arrangement of bonds around each carbon atom is tetrahedral, with a bond angle of approximately 109.5°.
A skeletal formula is a simplified way of representing an organic molecule. Hydrogen atoms bonded to carbon are omitted, showing only the carbon skeleton and any functional groups attached.
2-methylbutane as a condensed structural formula: the CH3 branch on carbon 2 makes the carbon skeleton branched. Its displayed and skeletal formulae show the same skeleton.
Ethane can be represented with all C-H and C-C covalent bonds shown.
But-2-ene uses a skeletal formula, with carbon atoms at line ends and vertices.
Functional groups, such as OH in alcohols, are shown explicitly in skeletal formulae.
Exam focus: In skeletal formulae, carbon atoms and carbon-bonded hydrogen atoms are usually not written, but heteroatoms and functional groups must still be shown.
Quick Check: Read a Skeletal Formula
Picture the skeletal formula described and work out its molecular formula.
Watch: finding the longest chain
A structural formula becomes a displayed formula, then the hunt for the longest carbon chain. Which end is carbon 1?
Naming Carbon Chains
The first step in IUPAC naming is to identify and count the longest continuous carbon chain. This gives the parent name of the compound.
Next, identify any branched side chains and count the number of carbon atoms in each branch. The correct prefix is then added to the parent name.
| Code | Number of carbons | Used in parent names such as |
|---|---|---|
| meth | 1 | methane |
| eth | 2 | ethane, ethene |
| prop | 3 | propane, propene |
| but | 4 | butane, but-2-ene |
| pent | 5 | pentane |
| hex | 6 | hexane |
| hept | 7 | heptane |
| oct | 8 | octane |
| non | 9 | nonane |
| dec | 10 | decane |
The longest continuous chain is counted first, then methyl branches are located using numbers.
Quick Check: Find the Longest Chain
Name a branched alkane whose longest chain is not the one written in a straight line.
Functional Groups and Suffix Rules
A functional group is an atom or group of atoms responsible for giving a homologous series its characteristic chemical reactions. In names, a functional group may be shown using either a prefix or a suffix.
Suffix starts with a vowel
If the suffix starts with a vowel, the final -e is removed from the parent alkane name. Examples include propan-1-ol, butan-1-amine, ethanoic acid, ethanoyl chloride and butanamide.
Suffix starts with a consonant
If the suffix starts with a consonant, the final -e is not removed from the parent alkane name. Examples include propanenitrile and pentane-2,4-dione.
Two or more of the same functional group
If there are two or more of the same functional group and di- or tri- is used, the final -e is not removed. Examples include ethane-1,2-diol and propane-1,2,3-triol.
The number 1 shows that the OH group is attached to the first carbon in the chain.
Quick Check: Keep the e or Drop It?
Drag the correctly written name to each of five compounds that are not on this page.
Numbering Rules and Alphabetical Order
Numbers are only included in names when they are needed to avoid ambiguity. When numbering a carbon chain, functional groups take priority over branched side chains when assigning the lowest possible number.
Words and numbers in organic names are separated using dashes. When more than one number is used, numbers are separated by commas.
If a molecule contains more than one functional group or side chain, the groups are listed in alphabetical order, ignoring multiplicative prefixes such as di- or tri-.
2,2-dichloro-1-fluorobutane shows comma-separated numbers and alphabetical ordering by functional group prefix.
Bromo is written before fluoro because prefixes are listed alphabetically.
Remember: The correct name depends on choosing the longest chain, assigning the lowest possible numbers and writing substituents in alphabetical order.
An IUPAC name is built from locants, prefixes in alphabetical order, a stem for the chain length and a suffix for the principal group.
Quick Check: Naming in the Right Order
Put the steps for naming a branched alcohol into the order in which you would carry them out.
Homologous Series and Functional Group Priority
A homologous series is a family of organic compounds with the same functional group and the same general formula.
Members of a homologous series show a gradual change in physical properties as chain length increases, but similar chemical properties because they contain the same functional group.
Each successive compound in a homologous series differs from the previous compound by a CH2 unit.
| Priority rule | What it means | Example exam wording |
|---|---|---|
| Highest priority group | The functional group with the highest priority is given the suffix and the lowest possible number. | Identify the principal functional group before numbering the chain. |
| Other functional groups | Other functional groups are named using prefixes. | Halogeno groups such as bromo, chloro and fluoro are written as prefixes. |
| Double and triple bonds | Alkenes and alkynes use suffixes even when another functional group is present. | Name the carbon chain and include the position of the C=C bond if required. |
Functional group priority, highest to lowest: carboxylic acids > aldehydes > ketones > alcohols > alkenes > halogenoalkanes.
Cyclohexene contains a C=C double bond in a cyclic carbon skeleton.
Cyclohexane is saturated because it contains carbon-carbon single bonds only.
The highest-priority group takes the suffix and the lowest number; groups lower down the ladder become prefixes.
Quick Check: Spot the Correct Name
In each round pick the one accurate statement about a name or a homologous series.
IUPAC Naming FAQs
These questions cover the naming steps that cost the most marks.
How do I find the parent chain?
Find the longest continuous chain of carbon atoms, even if it bends round a corner in the drawing. That chain gives the stem, such as pent- for five carbons.
When does the final -e of the alkane name drop?
Drop it when the suffix starts with a vowel, as in propan-1-ol. Keep it before a consonant or before di- or tri-, as in ethane-1,2-diol.
Which end of the chain do I number from?
Number from the end that gives the principal functional group the lowest number. Side chains and halogens only decide the numbering when there is a tie.
Does the di- in dichloro count for alphabetical order?
No. Ignore multiplying prefixes such as di- and tri-. Dichloro is listed under c, so 2,2-dichloro-1-fluorobutane has chloro before fluoro.
What is the difference between a structural and a displayed formula?
A structural formula shows the arrangement of atoms with minimal detail, such as CH3CH2OH. A displayed formula shows every atom and every covalent bond.
Copyright notice: This OLS revision content, including the explanations, layout, diagrams, tables and embedded learning structure, is authored for Online Learning System by Dr. Mohammed Al-Fatah. It may not be copied, reproduced, redistributed or adapted without written permission.
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