Topic 2 of 9
Alkanes: build a valid carbon skeleton
Use four bonds per carbon and one per hydrogen.
O-Level 6092 (2026) / SEC G3 K324 (2027)
Alkanes: build a valid carbon skeleton
Use four bonds per carbon and one per hydrogen.
A homologous series has a common general formula, similar chemical properties and a gradual change in physical properties as molecule size and mass increase. Successive members differ by CH2. Alkanes are saturated hydrocarbons: all carbon-carbon bonds are single. For an unbranched or branched acyclic alkane, the general formula is CnH2n+2.
| Name | Molecular formula | Condensed structure |
|---|---|---|
| Methane | CH4 | One C with four C-H bonds |
| Ethane | C2H6 | CH3-CH3 |
| Propane | C3H8 | CH3-CH2-CH3 |
To draw a displayed formula, draw the carbon-carbon connections first, then add individual C-H bonds until each carbon has four bonds. A condensed CH3 group stands for three separate hydrogens bonded to that carbon. Count atoms after drawing; moving the page or bending a chain does not create a new compound.
Four bonds around carbon
Methane has four single C-H bonds. Each ethene carbon has two C-H bonds and a double C=C bond, giving four bonds in total.
Displayed methane
Complete displayed structure with 1 carbon, 4 hydrogen atoms: CH4. Every bond and hydrogen is shown.
Displayed ethane
Complete displayed structure with 2 carbon, 6 hydrogen atoms: C2H6. Every bond and hydrogen is shown.
Displayed propane
Complete displayed structure with 3 carbon, 8 hydrogen atoms: C3H8. Every bond and hydrogen is shown.
Displayed butane
Complete displayed structure with 4 carbon, 10 hydrogen atoms: C4H10. Every bond and hydrogen is shown.
Displayed branched C4 alkane
Complete displayed structure with 4 carbon, 10 hydrogen atoms: C4H10. Every bond and hydrogen is shown.
| Structure | Condensed representation |
|---|---|
| Unbranched butane | CH3-CH2-CH2-CH3 |
| Branched C4H10 | CH3-CH(CH3)-CH3 |
Isomers have the same molecular formula but different structural formulae: their atoms are connected differently. These two C4H10 structures are isomers. A branch changes connectivity; simply drawing unbranched butane as a bent line does not.
Alkanes are generally unreactive, but burn and undergo substitution with chlorine in ultraviolet light. Complete combustion: CH4(g) + 2O2(g) -> CO2(g) + 2H2O(l), showing cooled products. Limited oxygen can produce carbon monoxide and/or soot. Substitution: CH4(g) + Cl2(g) -> CH3Cl(g) + HCl(g), under UV. One H is replaced by Cl; further substitution is possible.