Chemistry • Year 12 • Module 7 • Lesson 11
Combustion of Alcohols & Comparison with Fossil Fuels
Lock in the core vocabulary, the three-step calorimetry calculation, combustion equations, and the systematic sources of discrepancy in spirit burner experiments.
1. Term–definition match
Write the correct term from the list below next to each definition. 8 marks (1 per row)
Term bank: complete combustion • molar enthalpy of combustion (ΔHc) • energy density • bomb calorimeter • carbon neutrality • spirit burner calorimeter • systematic error • incomplete combustion
| # | Definition | Term |
|---|---|---|
| 1.1 | A reaction of a fuel with excess oxygen in which the only products are CO2(g) and H2O(g). | |
| 1.2 | The heat released when one mole of a substance burns completely in excess oxygen under standard conditions. | |
| 1.3 | The energy released per gram of fuel (kJ/g); calculated as |ΔHc| ÷ molar mass. | |
| 1.4 | A closed, oxygen-pressurised vessel that measures combustion heat with minimal heat loss; gives results close to theoretical ΔHc. | |
| 1.5 | A fuel property where the CO2 released on combustion equals the CO2 absorbed from the atmosphere during biomass growth. | |
| 1.6 | A simple open-flame apparatus used in school labs; a spirit burner heats water in a copper can using q = mcΔT. | |
| 1.7 | An error that consistently shifts all results in one direction; it does not average out with repeat trials. | |
| 1.8 | Combustion in limited oxygen producing CO and/or soot (C) rather than fully converting to CO2. |
2. True or false — with correction
Circle T or F. If the statement is false, write the corrected version on the line. 8 marks (1 T/F + 1 correction where needed)
2.1 In the formula q = mcΔT, m refers to the mass of alcohol burned in the spirit burner. T / F
2.2 The experimental ΔHc from a spirit burner is always lower in magnitude than the theoretical value. T / F
2.3 Longer-chain alcohols have a smaller molar enthalpy of combustion because their molecules are larger and harder to burn. T / F
2.4 Both ethanol and octane (petrol) produce only CO2 and H2O in complete combustion. T / F
3. Cloze — fill the blanks
Complete the paragraph using the word bank. Each word is used once. 8 marks (1 per blank)
Word bank: exothermic • kJ/mol • negative • joules • water • moles • theoretical • systematic
In a spirit burner experiment, heat released by combustion is absorbed by the (3.1) __________ in the calorimeter. Using q = mcΔT gives the heat in (3.2) __________. Dividing q (converted to kJ) by the number of (3.3) __________ of alcohol burned gives ΔHc in (3.4) __________. Because combustion is (3.5) __________, the value of ΔHc is always (3.6) __________. The experimental result is consistently lower than the (3.7) __________ value because heat is lost to the surroundings — this is a (3.8) __________ error, not a random one.
4. Balance the combustion equations
Write balanced equations for complete combustion of each alcohol in excess oxygen. Include state symbols (l) and (g). 6 marks (2 each)
4.1 Methanol (CH3OH)
CH3OH(l) + _____ O2(g) → _____ CO2(g) + _____ H2O(g)
4.2 Ethanol (C2H5OH)
C2H5OH(l) + _____ O2(g) → _____ CO2(g) + _____ H2O(g)
4.3 Propan-1-ol (C3H7OH)
C3H7OH(l) + _____ O2(g) → _____ CO2(g) + _____ H2O(g)
5. Sources of discrepancy — match the chain
Link each source of error to its effect on q or n, then to its effect on |ΔHc|. Write A, B, or C in each blank. 6 marks
Sources:
- Heat loss to surroundings (calorimeter walls, air, bench)
- Alcohol evaporating from wick without combustion
- Incomplete combustion producing CO and soot
| Effect on measurement | Measurement affected (q or n) | Source letter (A, B, or C) |
|---|---|---|
| Less heat captured by water; measured heat lower than actual heat released | q too low | |
| Mass decrease recorded but no combustion heat produced; n inflated relative to heat released | n too high | |
| Fuel oxidised to CO and C not CO2; chemical energy retained in products not released as heat | q too low |
5.4 All three sources make the calculated |ΔHc| __________ (higher / lower) than the theoretical value. This is because they are __________ (systematic / random) errors. 2 marks
Q1 — Term–definition match
1.1 complete combustion • 1.2 molar enthalpy of combustion (ΔHc) • 1.3 energy density • 1.4 bomb calorimeter • 1.5 carbon neutrality • 1.6 spirit burner calorimeter • 1.7 systematic error • 1.8 incomplete combustion
Q2 — True/False with correction
2.1 False. Correction: m in q = mcΔT is the mass of water in the calorimeter, not the mass of alcohol burned. The water temperature rise is what is measured; the alcohol mass (fuel burned) is used in Step 2: n = Δm/M.
2.2 True. The experimental ΔHc is always lower in magnitude because of heat loss to surroundings, incomplete combustion, and alcohol evaporation — all systematic errors.
2.3 False. Correction: longer-chain alcohols have a larger magnitude ΔHc. Each additional CH2 unit adds C–H and C–C bonds whose combustion releases approximately 650 kJ/mol of extra energy. The claim confuses chain length with combustion difficulty.
2.4 True. Complete combustion of both ethanol and octane produces only CO2(g) and H2O(g). The sustainability difference lies in the carbon cycle, not combustion products.
Q3 — Cloze
3.1 water • 3.2 joules • 3.3 moles • 3.4 kJ/mol • 3.5 exothermic • 3.6 negative • 3.7 theoretical • 3.8 systematic
Q4 — Combustion equations
4.1 CH3OH(l) + 3/2 O2(g) → CO2(g) + 2H2O(g) or multiplied through: 2CH3OH(l) + 3O2(g) → 2CO2(g) + 4H2O(g). Accept fractional coefficients.
4.2 C2H5OH(l) + 3O2(g) → 2CO2(g) + 3H2O(g)
4.3 C3H7OH(l) + 9/2 O2(g) → 3CO2(g) + 4H2O(g) or: 2C3H7OH(l) + 9O2(g) → 6CO2(g) + 8H2O(g).
Marking notes: 1 mark for correct products (CO2 + H2O only), 1 mark for balanced coefficients including O2. State symbols optional at this tier but award both marks if correct.
Q5 — Sources of discrepancy
Row 1 (q too low, heat loss): Source A
Row 2 (n too high, evaporation): Source B
Row 3 (q too low, incomplete combustion): Source C
5.4 All three make |ΔHc| lower than theoretical. They are systematic errors (always in the same direction; do not average out with repeat trials).