Organic Chemistry – Formulae, Functional Groups and Terminology (Cambridge IGCSE 0620)
Learning Objective
State that a saturated compound has molecules in which all carbon‑carbon bonds are single bonds (no C=C or C≡C bonds). This wording matches the Cambridge syllabus exactly.
Key Definitions (core)
Organic compound: Contains carbon, usually bonded to hydrogen, and may also contain O, N, halogens, etc.
Saturated hydrocarbon (alkane): Every C–C bond is a single bond. General formula CnH2n+2.
Unsaturated hydrocarbon: Contains one or more C=C double bonds (alkenes) or C≡C triple bonds (alkynes). Only alkenes are required for the IGCSE core.
Alkene: An unsaturated hydrocarbon with at least one C=C double bond. General formula CnH2n.
Alcohol: Contains a hydroxyl group (‑OH) attached to a saturated carbon. General formula CnH2n+2O (≤ 4 C).
Carboxylic acid: Contains a carboxyl group (‑COOH). General formula CnH2nO2 (≤ 4 C).
Functional group: A specific arrangement of atoms that determines the characteristic chemical behaviour (e.g., ‑OH, C=C, ‑COOH).
Structural isomer: Compounds with the same molecular formula but different connectivity of atoms.
Core Classes & General Formulae (≤ 4 C)
Class of compound
General formula
Typical functional group
Alkane (saturated)
CnH2n+2
None (only C–C & C–H)
Alkene (unsaturated)
CnH2n
C=C (double bond)
Alcohol
CnH2n+2O
‑OH (hydroxyl)
Carboxylic acid
CnH2nO2
‑COOH (carboxyl)
Only the four classes above are required for the core syllabus.
Why Saturated Compounds Are Called “Saturated”
Each carbon atom has formed the maximum possible number of single covalent bonds with hydrogen**. Adding another hydrogen would require breaking an existing C–C single bond, which is not possible without a chemical reaction. In other words, the molecule is “full” – or saturated – with hydrogen.
In the exam you will be asked to draw or interpret bond‑line (displayed) formulas. Remember:
Each vertex (or line end) = a carbon atom.
Hydrogen atoms attached to carbon are **implicit** – you do not write them.
Double bonds are shown as “=”, triple bonds as “≡”. (Only double bonds are required for the core.)
Functional groups (‑OH, ‑COOH, etc.) are drawn explicitly.
Examples
1. Alkane – n‑butane (C4H10)
H H H H
| | | |
H–C–C–C–C–H
| | |
H H H
2. Alkene – but‑2‑ene (C4H8) – note the double bond position
H H H H
| | | |
H–C–C = C–C–H
| |
H H
3. Alcohol – ethanol (C2H6O)
H H
| |
H–C–C–O–H
| |
H H
4. Carboxylic acid – propanoic acid (C3H6O2)
H H
| |
H–C–C–C–O–H
||
O
Placement of Double Bonds
When a molecule contains more than one possible double‑bond location (e.g., but‑1‑ene vs. but‑2‑ene) you must show the exact position in the bond‑line diagram. This is a common exam pitfall.
Naming Unbranched Compounds (core requirement)
Displayed formula
Common name
IUPAC name (≤ 4 C)
CH₃‑CH₃
Methane
Methane
CH₃‑CH₂‑CH₃
Propane
Propane
CH₃‑CH₂‑CH₂‑CH₃
Butane
Butane
CH₃‑CH=CH‑CH₃
But‑2‑ene
But‑2‑ene
CH₂=CH‑CH₂‑CH₃
But‑1‑ene
But‑1‑ene
CH₃‑CH₂‑OH
Ethanol
Ethanol
CH₃‑CH₂‑COOH
Propanoic acid
Propanoic acid
Structural Isomers (supplementary topic)
Only C₄H₁₀ isomers are required for the supplement. You should be able to:
Identify the two isomers (n‑butane and isobutane).
Alkynes contain C≡C triple bonds and are not listed in the 0620 syllabus. They are omitted to keep the core focused on alkanes, alkenes, alcohols and carboxylic acids.
State Symbols (required for symbol equations)
(s) – solid
(l) – liquid
(g) – gas
(aq) – aqueous solution
Example symbol equation (combustion of ethane):
C₂H₆(g) + 7 O₂(g) → 4 CO₂(g) + 6 H₂O(l)
Common Misconceptions
“All organic compounds are saturated.” – False. Alkenes have C=C double bonds and are unsaturated.
“A compound with a functional group cannot be saturated.” – False. Saturation refers only to the carbon skeleton. Ethanol (CH₃CH₂OH) is saturated because its C‑C bonds are all single.
“Alkynes are part of the IGCSE core.” – False. They are excluded from the 0620 syllabus.
“Hydrogen can be added to any organic molecule to make it saturated.” – False. Hydrogen can only be added if the carbon skeleton already contains only single C‑C bonds; otherwise a bond must be broken first.
Quick‑Check Questions
Write the molecular formula for the saturated hydrocarbon containing five carbon atoms.
Is cyclohexane (C₆H₁₂) saturated or unsaturated? Explain using the definition of saturation.
Identify the functional group in CH₃CH₂COOH and name the compound.
Draw the bond‑line (displayed) formula for prop‑1‑ene (C₃H₆).
Give the IUPAC name for the displayed formula
CH₃‑CH(CH₃)‑CH₃
.
Write a balanced symbol equation (including state symbols) for the combustion of ethane.
Answers to Quick‑Check
C₅H₁₂ (using CₙH₂ₙ₊₂ for alkanes).
Cyclohexane is saturated. Although it is a ring, each carbon is bonded to two other carbons and two hydrogens – all C‑C bonds are single, satisfying the definition.
Functional group: **carboxyl** (‑COOH). The compound is **propanoic acid**.
Bond‑line for prop‑1‑ene:
H H
| |
H–C = C–C–H
| |
H H
The name is **2‑methylpropane** (commonly called isobutane).
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