Topic 4 of 7
Alcohols: identify -OH and follow ethanol
Structure connects preparation, combustion and oxidation.
O-Level 5086 / 5088 (2026) / SEC G3 K326 / K328 (2027)
Alcohols: identify -OH and follow ethanol
Structure connects preparation, combustion and oxidation.
Alcohols form a homologous series containing the -OH functional group. The group is covalently attached within a molecule; it is not a free hydroxide ion, so the presence of -OH does not make ethanol an alkali.
| Name | Condensed structure |
|---|---|
| Methanol | CH3-OH |
| Ethanol | CH3-CH2-OH |
| Propan-1-ol | CH3-CH2-CH2-OH |
| Propan-2-ol | CH3-CH(OH)-CH3 |
Expand condensed structures by showing each bond to H separately and checking C has four bonds and O two. Moving -OH along the carbon chain changes the structure, even when the carbon skeleton remains unbranched.
Displayed methanol
Complete displayed structure with 1 carbon, 4 hydrogen and 1 oxygen atoms: CH4O. Every bond and hydrogen is shown.
Displayed ethanol
Complete displayed structure with 2 carbon, 6 hydrogen and 1 oxygen atoms: C2H6O. Every bond and hydrogen is shown.
Displayed propan-1-ol
Complete displayed structure with 3 carbon, 8 hydrogen and 1 oxygen atoms: C3H8O. Every bond and hydrogen is shown.
Displayed propan-2-ol
Complete displayed structure with 3 carbon, 8 hydrogen and 1 oxygen atoms: C3H8O. Every bond and hydrogen is shown.
- Feedstock
Glucose solution, obtainable from sugarcane sugars.
- Conditions
Yeast supplies enzymes; keep warm and exclude oxygen. Excessive heat damages enzymes.
- Reaction
C6H12O6(aq) -> 2C2H5OH(aq) + 2CO2(g).
- Recovery
Fractional distillation separates ethanol-rich liquid from the fermentation mixture.
Ethanol burns in sufficient oxygen: C2H5OH(l) + 3O2(g) -> 2CO2(g) + 3H2O(l), after cooling. It can also be oxidised to ethanoic acid by atmospheric oxygen, or by warming with acidified potassium manganate(VII). In shorthand, CH3CH2OH + 2[O] -> CH3COOH + H2O; [O] denotes oxygen supplied by an oxidising agent.
Use ethanol as the representative alcohol-to-acid conversion here. Do not assume that every possible alcohol structure gives a carboxylic acid: the position of -OH matters, and detailed alternative oxidation pathways are beyond these Secondary outcomes.