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Year 11 Chemistry Module 4 ⏱ ~45 min Lesson 10 of 13

Hess's Law Applied — Heat of Combustion & Consolidation

Engineers designing a car to run on ethanol vs octane need to know which fuel delivers more energy — per mole, per gram, and per litre. They calculate these values entirely on paper using the three methods you have built across Lessons 6–9. This lesson puts them all together: when to use bond energies, when to use ΔH°f values, and when Hess's Law is the only option.

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Think First — Misconception Challenge

A fuel with a larger ΔHc (enthalpy of combustion in kJ mol⁻¹) always gives you more energy for a given mass of fuel. True or false?

Think about ethanol (C₂H₅OH, ΔHc = −1367 kJ mol⁻¹, M = 46.07 g mol⁻¹) vs methanol (CH₃OH, ΔHc = −726 kJ mol⁻¹, M = 32.04 g mol⁻¹). Ethanol releases almost twice as much energy per mole. But if you fill a fuel tank by mass — which fuel gives you more energy per kilogram?

Before this lesson: Calculate (or estimate) energy per gram for each fuel. Does the fuel with higher ΔHc per mole also have higher energy per gram? Write your prediction with any working.

Type your prediction below — you will revisit this at the end of the lesson.

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📐

Formula Reference — This Lesson

Bond energy: $\Delta H = \Sigma B(\text{reactants}) - \Sigma B(\text{products})$
Reactants first. Use average bond enthalpies (kJ mol⁻¹). Approximate — assumes gaseous state.
Enthalpy of formation: $\Delta H^\circ_{rxn} = \Sigma\Delta H^\circ_f(\text{products}) - \Sigma\Delta H^\circ_f(\text{reactants})$
Products first. Multiply each ΔH°f by stoichiometric coefficient. More accurate than bond energy.
Hess's Law: $\Delta H(\text{target}) = \Sigma(\Delta H_\text{steps})$ with sign and scale corrections
Add manipulated equations; cancel intermediates; as accurate as the input data.
Energy per gram: $E_g = \dfrac{|\Delta H_c|}{M}$   (kJ g⁻¹)
|ΔHc| = magnitude of molar enthalpy of combustion (kJ mol⁻¹)  |  M = molar mass (g mol⁻¹) Use this to compare fuels by mass — relevant when fuelling by weight (aircraft, ships)
📖 Know

Key Facts

  • Energy per gram = |ΔHc| ÷ M (kJ g⁻¹) — the mass-based fuel comparison
  • Bond energy method → approximate; ΔH°f method → more accurate; Hess's Law → depends on data quality
  • ΔH°f method and Hess's Law combustion cycle are mathematically equivalent
💡 Understand

Concepts

  • Why the three ΔH calculation methods are equivalent when applied to the same reaction
  • Why a higher ΔHc per mole does not guarantee higher energy per gram
  • How to select the correct method from the data provided in an HSC question
✅ Can Do

Skills

  • Calculate ΔHc using ΔH°f data (products − reactants, scaled coefficients)
  • Calculate and compare energy per gram for two fuels
  • Identify which ΔH method to use from question context and data type provided
Key Terms — scan these before reading
Enthalpy change (ΔH)The heat energy exchanged at constant pressure during a reaction.
ExothermicA reaction releasing heat to surroundings (ΔH < 0).
EndothermicA reaction absorbing heat from surroundings (ΔH > 0).
CalorimetryThe experimental measurement of heat changes during chemical processes.
Hess's LawThe total enthalpy change is independent of the pathway taken.
EntropyA measure of the disorder or randomness of a system.
02

Comparing the Three Methods — When to Use Each

In HSC, the method is almost always signalled by the data provided. The question tells you which method to use — your job is to recognise the signal and apply the correct procedure.

Table of bond enthalpies only

Method to use: Bond energy method
Accuracy: Approximate (±5–20%)
Key formula: ΔH = ΣB(reactants) − ΣB(products)

Table of ΔH°f values

Method to use: Enthalpy of formation method
Accuracy: More accurate
Key formula: ΔH°rxn = ΣΔH°f(products) − ΣΔH°f(reactants)

Set of thermochemical equations

Method to use: Hess's Law
Accuracy: Depends on input data quality
Key formula: Add/reverse/scale equations; cancel intermediates

Mix of ΔH°f and experimental ΔH

Method to use: Hess's Law
Accuracy: High if data is precise
Key formula: Same as above

Why do the methods give different numerical results?

  • Bond energy: uses average values across many molecular contexts; assumes all species are gaseous (even liquids); introduces cumulative error across multiple bonds
  • ΔH°f: uses experimentally measured values for each specific substance in its actual state at 25°C; no averaging; matches real conditions → most accurate for standard conditions
  • Hess's Law: inherits the accuracy of whatever ΔH values are used as input; if using precise experimental values → highly accurate; if using estimated values → less so
Never use the bond energy method when ΔH°f data is provided. This wastes time, introduces unnecessary error, and in questions that specify the method ("using the data provided, calculate…"), may not receive full marks. Always match your method to the data type given.
Deeper connection: All three methods are ultimately expressions of the same underlying principle — Hess's Law and energy conservation. Bond energy sums the bond-breaking/forming cycle for gaseous species. ΔH°f method uses a Hess's Law cycle via elements. Multi-step Hess's Law combines experimental reactions directly. The differences are in data source and precision, not in principle.
HESS'S LAW CYCLE — INTERACTIVE Interactive
Compare all three example cycles — C→CO₂, photosynthesis/respiration, and NH₃ formation.
03

Comparing Fuel Efficiency — Per Mole vs Per Gram

Molar enthalpy of combustion (kJ mol⁻¹) is the chemist's comparison. Energy per gram (kJ g⁻¹) is the engineer's comparison. Neither is universally "better" — you must specify which comparison you are making.

Fuel choice in Australian transport policy. Ethanol blends (E10, E85) are used in Australian petrol. The debate about whether ethanol is a good fuel additive involves exactly this comparison: ethanol has lower energy per gram than octane, but it is renewable, reduces net CO₂ emissions (carbon-neutral cycle), has a higher octane rating (reduces engine knock), and can be produced domestically from sugarcane or grain. Pure thermochemistry gives part of the answer — the rest is economics and sustainability.

Fuel efficiency data — selected fuels:

FuelFormulaM (g mol⁻¹) ΔHc (kJ mol⁻¹)Energy per gram (kJ g⁻¹)
HydrogenH₂(g)2.02−286141.6
Methane (natural gas)CH₄(g)16.04−89055.5
Octane (petrol)C₈H₁₈(l)114.23−547147.9
EthanolC₂H₅OH(l)46.07−136729.7
MethanolCH₃OH(l)32.04−72622.7

Key observations from the data:

Energy per Gram — Fuel Comparison (kJ g⁻¹) kJ g⁻¹ 141.6 H₂ hydrogen 55.5 CH₄ methane 47.9 C₈H₁₈ octane 29.7 C₂H₅OH ethanol 22.7 CH₃OH methanol
Energy per gram comparison for five fuels. Hydrogen dominates by mass — 141.6 kJ g⁻¹ vs octane's 47.9 kJ g⁻¹. Ethanol and methanol lag behind octane on this metric, despite ethanol releasing more kJ mol⁻¹ than methanol.
Common misconception resolved: "The fuel with higher ΔHc per mole gives more energy per gram." False — a higher molar enthalpy does not guarantee higher energy per gram. You must divide by molar mass: E(per gram) = |ΔHc| ÷ M. Ethanol has higher ΔHc per mole than methanol, AND higher energy per gram — but this is because of its particular combination of ΔHc and M. The relationship is not automatic.
FUEL ENERGY COMPARISON — kJ mol⁻¹ vs kJ g⁻¹ ΔHc per mole (kJ mol⁻¹) 726 Methanol 1367 Ethanol 2020 Propanol 5471 Octane 286 (×10) Hydrogen×10 Energy per gram (kJ g⁻¹) 22.7 Methanol 29.7 Ethanol 33.6 Propanol 47.9 Octane 141.8 Hydrogen
⚠️

Common Misconceptions — IQ2 Consolidation

Higher ΔHc per mole always means more energy per gram.

Why students think this: ΔHc is the most visible number and larger magnitude seems "better."

What is actually true: Energy per gram = |ΔHc| ÷ M. A fuel can have large ΔHc per mole but low energy per gram if its molar mass is large. Always calculate both before comparing fuels.

The bond energy method and ΔH°f method always give the same ΔH for a reaction.

Why students think this: Both methods calculate ΔH for the same reaction, so the answer should be the same.

What is actually true: Bond energies are averages for bond types across many molecules; ΔH°f values are experimentally measured for specific substances in actual states. They give different numerical results, with ΔH°f being more accurate. Only under ideal conditions (all gas-phase species, exact bond energies) would they agree.

Hess's Law only works when you have exactly two equations to add together.

Why students think this: The NESA prototype (L08) uses two equations, and students generalise from this.

What is actually true: Hess's Law works with any number of equations. The worked example in L08 used three equations. The ΔH°f method is implicitly a Hess's Law cycle using as many formation equations as there are species in the balanced equation. The principle (path independence of enthalpy) is not limited by the number of steps.

📒 Copy Into Your Books

Method Selection Guide

  • Bond energies given → bond energy method (approximate)
  • ΔHf° table given → enthalpy of formation method (accurate)
  • Thermochemical equations given → Hess's Law
  • Never use bond energy method when ΔHf° data is available

Energy per Gram Calculation

  • E (kJ g⁻¹) = |ΔHc| ÷ M
  • Higher ΔHc per mole ≠ higher energy per gram
  • Hydrogen: 141.6 kJ g⁻¹ | Octane: 47.9 | Ethanol: 29.7

The Three Methods — Key Differences

  • Bond energy: ΔH = ΣB(react) − ΣB(prod). Reactants first. Approximate.
  • ΔHf°: ΔH = ΣΔHf°(prod) − ΣΔHf°(react). Products first. Accurate.
  • Hess's Law: add equations, cancel intermediates, sum ΔH.

Hess's Law Combustion Cycle

  • Triangle: elements → fuel, elements → products, fuel → products
  • ΔHf°(fuel) + ΔHc = ΣΔHf°(products)
  • ∴ ΔHc = ΣΔHf°(products) − ΔHf°(fuel) — identical to ΔHf° formula

🔬 Worked Examples

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Example 1 — Enthalpy of Combustion of Propan-1-ol

Calculate the standard enthalpy of combustion of propan-1-ol (C₃H₇OH) using ΔH°f data:
C₃H₇OH(l) + 9/2 O₂(g) → 3CO₂(g) + 4H₂O(l)
ΔH°f values: C₃H₇OH(l) = −303 kJ mol⁻¹  |  CO₂(g) = −393.5 kJ mol⁻¹  |  H₂O(l) = −285.8 kJ mol⁻¹  |  O₂(g) = 0

GIVEN / FIND
GIVEN: Balanced combustion equation with state symbols; ΔH°f values for all species
FIND: ΔH°rxn (= ΔHc) using ΔH°rxn = ΣΔH°f(products) − ΣΔH°f(reactants)
Step 1 — Sum ΔH°f(products): multiply each by coefficient
Products: 3 mol CO₂(g) + 4 mol H₂O(l)

ΣΔH°f(products) = 3(−393.5) + 4(−285.8)
                        = −1180.5 + (−1143.2)
                        = −2323.7 kJ mol⁻¹
Each ΔH°f value is multiplied by its stoichiometric coefficient from the balanced equation.
Step 2 — Sum ΔH°f(reactants): multiply each by coefficient
Reactants: 1 mol C₃H₇OH(l) + 9/2 mol O₂(g)

ΣΔH°f(reactants) = 1(−303) + (9/2)(0)
                         = −303 + 0
                         = −303 kJ mol⁻¹
O₂ has ΔH°f = 0; show this step explicitly even though it contributes nothing numerically.
Step 3 — Apply formula: products minus reactants
ΔH°rxn = ΣΔH°f(products) − ΣΔH°f(reactants)
           = −2323.7 − (−303)
           = −2323.7 + 303
           = −2020.7 kJ mol⁻¹

Exothermic combustion — expected. Accepted value for ΔHc[propan-1-ol] = −2021 kJ mol⁻¹. Essentially exact, as expected with ΔH°f data.
🎯 Try It Now

Calculate the energy per gram released by propan-1-ol. (M = 60.10 g mol⁻¹, ΔHc = −2020.7 kJ mol⁻¹.) Then compare to ethanol (29.7 kJ g⁻¹). Which releases more energy per gram?

E per gram = |ΔHc| ÷ M = 2020.7 ÷ 60.10 = 33.6 kJ g⁻¹

Comparison: propan-1-ol (33.6 kJ g⁻¹) releases more energy per gram than ethanol (29.7 kJ g⁻¹), even though ethanol has a higher ΔHc per mole? Wait — let's check: ethanol ΔHc = −1367 kJ mol⁻¹, M = 46.07 → 1367/46.07 = 29.7 kJ g⁻¹. Yes — propan-1-ol is more energy-dense per gram, despite having a larger molecule and larger absolute ΔHc per mole. This confirms that molar mass matters: propan-1-ol's gain in ΔHc outpaces its gain in molar mass relative to ethanol.
💡

Example 2 — Fuel Efficiency Comparison: Methanol vs Ethanol

Methanol (CH₃OH, M = 32.04 g mol⁻¹, ΔHc = −726 kJ mol⁻¹) and ethanol (C₂H₅OH, M = 46.07 g mol⁻¹, ΔHc = −1367 kJ mol⁻¹) are compared as alternative automotive fuels.
(a) Which releases more energy per mole? (b) Which releases more energy per gram? (c) Suggest two reasons other than energy content why ethanol is often preferred as a fuel additive over methanol.

Part (a) — Per mole comparison
Methanol: |ΔHc| = 726 kJ mol⁻¹
Ethanol: |ΔHc| = 1367 kJ mol⁻¹

Ethanol releases more energy per mole — 1367 vs 726 kJ mol⁻¹ (almost twice as much).
Direct comparison of ΔHc magnitudes. Ethanol has twice as many carbon atoms and three additional C–H bonds, explaining the higher ΔHc.
Part (b) — Per gram comparison
Methanol energy per gram = 726 ÷ 32.04 = 22.7 kJ g⁻¹
Ethanol energy per gram = 1367 ÷ 46.07 = 29.7 kJ g⁻¹

Ethanol also releases more energy per gram — 29.7 vs 22.7 kJ g⁻¹.

In this case, ethanol wins on both comparisons. But notice that the per-gram advantage is smaller than the per-mole advantage — the larger molar mass of ethanol (46.07 vs 32.04) partially offsets the ΔHc per mole advantage. For comparison: octane = 47.9 kJ g⁻¹ — both alcohols are significantly less energy-dense than petrol per gram.
Part (c) — Non-thermochemical reasons for ethanol preference
Two reasons why ethanol is preferred over methanol as a fuel additive (any two of the following):

1. Toxicity: Methanol is highly toxic — ingestion or inhalation of small quantities causes blindness and death. Ethanol is far less acutely toxic, reducing safety risk in handling and in fuel systems that might contaminate food or water.

2. Renewability/sustainability: Ethanol is efficiently produced by fermentation of plant sugars (sugarcane, corn) — a mature industrial process. Methanol is primarily produced from natural gas (non-renewable) via steam reforming.

3. Miscibility with petrol: Ethanol mixes more compatibly with conventional petrol at higher blend ratios and is less corrosive to existing fuel system components than methanol at equivalent blends.

This question illustrates that real-world fuel selection involves far more than thermochemical calculations alone. Engineering, economics, safety, and policy all interact.

🔬 Activities

🔬 Activity 1 — Calculate + Interpret

Calculating ΔHc for Ethane via Hess's Law

Use the thermochemical data below to calculate ΔHc for ethane — a situation where Hess's Law is required because ΔH°f[C₂H₆(g)] is not directly given.

Given thermochemical equations:

(1)   C(graphite) + O₂(g) → CO₂(g)                                            ΔH₁ = −393.5 kJ mol⁻¹
(2)   H₂(g) + ½O₂(g) → H₂O(l)                                                 ΔH₂ = −285.8 kJ mol⁻¹
(3)   C₂H₆(g) + 7/2 O₂(g) → 2CO₂(g) + 3H₂O(l)       ΔH₃ = −1560.7 kJ mol⁻¹
  1. a Write the target equation for the enthalpy of formation of ethane: the equation in which exactly 1 mol C₂H₆(g) is formed from its elements in standard states. Include state symbols.

    2C(graphite) + 3H₂(g) → C₂H₆(g)    ΔH = ΔH°f[C₂H₆(g)] = ?

    This is the formation equation: reactants are pure elements (C(graphite) and H₂(g)) in their standard states; product is exactly 1 mol C₂H₆(g).
  2. b Using Hess's Law with the three given equations, calculate ΔH°f[C₂H₆(g)]. Show each manipulation step (which equations to use, whether to reverse or scale, the modified ΔH values), cancel intermediates, and verify the target equation before summing.

    Target: 2C(graphite) + 3H₂(g) → C₂H₆(g)

    C(graphite): target needs 2 mol C as reactants. Equation (1) has 1 mol C as reactant — scale (1) by ×2: 2C + 2O₂ → 2CO₂, ΔH = 2(−393.5) = −787.0 kJ mol⁻¹
    H₂: target needs 3 mol H₂ as reactants. Equation (2) has 1 mol H₂ — scale (2) by ×3: 3H₂ + 3/2 O₂ → 3H₂O, ΔH = 3(−285.8) = −857.4 kJ mol⁻¹
    C₂H₆: target needs it as product. Equation (3) has it as reactant — reverse (3): 2CO₂ + 3H₂O → C₂H₆ + 7/2 O₂, ΔH = +1560.7 kJ mol⁻¹

    Add 2×(1) + 3×(2) + reverse(3):
    2C + 2O₂ + 3H₂ + 3/2 O₂ + 2CO₂ + 3H₂O → 2CO₂ + 3H₂O + C₂H₆ + 7/2 O₂
    Cancel: 2CO₂ both sides ✓ | 3H₂O both sides ✓ | 2O₂ + 3/2 O₂ − 7/2 O₂ = 0 ✓
    Remaining: 2C(graphite) + 3H₂(g) → C₂H₆(g) ✓

    ΔH = −787.0 + (−857.4) + 1560.7 = −83.7 kJ mol⁻¹

    ΔH°f[C₂H₆(g)] = −83.7 kJ mol⁻¹. Accepted value = −84.7 kJ mol⁻¹ — very close match.
  3. c Now write the balanced combustion equation for ethane and use your ΔH°f result to calculate ΔHc[C₂H₆(g)] using the ΔH°f formula. Use ΔH°f[C₂H₆(g)] = −83.7 kJ mol⁻¹.

    Balanced combustion: C₂H₆(g) + 7/2 O₂(g) → 2CO₂(g) + 3H₂O(l)

    ΣΔH°f(products) = 2(−393.5) + 3(−285.8) = −787.0 + (−857.4) = −1644.4 kJ mol⁻¹
    ΣΔH°f(reactants) = 1(−83.7) + 7/2(0) = −83.7 kJ mol⁻¹

    ΔHc = −1644.4 − (−83.7) = −1644.4 + 83.7 = −1560.7 kJ mol⁻¹

    This matches ΔH₃ from the given data — as expected, since ΔH₃ was the direct combustion enthalpy of ethane. The cycle is self-consistent.

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🔬 Activity 2 — Calculate + Interpret

Which Alcohol Fuel Is Most Efficient?

Use ΔH°f data to calculate the enthalpy of combustion of butanol, then compare alcohol fuels on a per-gram basis.

ΔH°f data (kJ mol⁻¹):

SubstanceΔH°f (kJ mol⁻¹)SubstanceΔH°f (kJ mol⁻¹)
CO₂(g)−393.5H₂O(l)−285.8
CH₃OH(l) methanol−239C₂H₅OH(l) ethanol−277.7
C₃H₇OH(l) propan-1-ol−303C₄H₉OH(l) butan-1-ol−327
O₂(g)0  
  1. a Write the balanced combustion equation for butan-1-ol (C₄H₉OH) and calculate ΔHc using the ΔH°f data above.

    Balanced combustion equation: C₄H₉OH(l) + 6O₂(g) → 4CO₂(g) + 5H₂O(l)

    ΣΔH°f(products) = 4(−393.5) + 5(−285.8) = −1574.0 + (−1429.0) = −3003.0 kJ mol⁻¹
    ΣΔH°f(reactants) = 1(−327) + 6(0) = −327 kJ mol⁻¹

    ΔHc = −3003.0 − (−327) = −3003.0 + 327 = −2676 kJ mol⁻¹
  2. b Complete the table below (calculate energy per gram for each alcohol). Then answer: does energy per gram consistently increase or decrease as the alcohol chain gets longer?
    Molar masses: methanol = 32.04; ethanol = 46.07; propan-1-ol = 60.10; butan-1-ol = 74.12 g mol⁻¹
    ΔHc values: methanol = −726; ethanol = −1367; propan-1-ol = −2021; butan-1-ol = your answer from (a).

    Methanol: 726 ÷ 32.04 = 22.7 kJ g⁻¹
    Ethanol: 1367 ÷ 46.07 = 29.7 kJ g⁻¹
    Propan-1-ol: 2021 ÷ 60.10 = 33.6 kJ g⁻¹
    Butan-1-ol: 2676 ÷ 74.12 = 36.1 kJ g⁻¹

    Trend: Energy per gram consistently increases as the alcohol chain lengthens (22.7 → 29.7 → 33.6 → 36.1 kJ g⁻¹). This is because each additional CH₂ group adds more bond energy per gram than the group's mass contribution — the C–H bond density increases relative to the O–H group which contributes less per gram. Longer-chain alcohols approach the energy per gram of alkanes (octane = 47.9 kJ g⁻¹).

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Revisit Your Initial Thinking

Look back at what you wrote in the Think First section. What has changed? What did you get right? What surprised you?

MC

Multiple Choice

5 random questions from a replayable lesson bank — feedback shown immediately

✍️ Short Answer

04

Extended Questions

ApplyBand 4

6. A student uses two different methods to calculate ΔH for the combustion of methane (CH₄(g) + 2O₂(g) → CO₂(g) + 2H₂O(l)).

Method 1 (Bond energy): Bond energies: C–H = 413; O=O = 498; C=O = 743 (in CO₂); O–H = 463 kJ mol⁻¹. ΔH = −674 kJ mol⁻¹
Method 2 (ΔH°f): ΔH°f: CH₄(g) = −74.8; CO₂(g) = −393.5; H₂O(l) = −285.8 kJ mol⁻¹. ΔH = −890.3 kJ mol⁻¹

(a) Which result is more accurate? Justify in terms of the data used. (2 marks)
(b) The bond energy method gave −674 kJ mol⁻¹ while ΔH°f gave −890.3 kJ mol⁻¹ — a difference of 216 kJ mol⁻¹. Identify and explain TWO specific reasons for this large discrepancy. (4 marks) 6 MARKS

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ApplyBand 4

7. Propan-1-ol (C₃H₇OH, M = 60.10 g mol⁻¹) and butan-1-ol (C₄H₉OH, M = 74.12 g mol⁻¹) are being evaluated as biofuel alternatives to octane.

(a) Using ΔH°f data from Activity 2, confirm ΔHc[propan-1-ol] = −2021 kJ mol⁻¹. (3 marks)
(b) Calculate the energy per gram for propan-1-ol and butan-1-ol (use ΔHc[butan-1-ol] = −2676 kJ mol⁻¹). Which has higher energy density per gram? (2 marks)
(c) Both values are lower than octane (47.9 kJ g⁻¹). Suggest one engineering advantage of alcohol fuels over octane that offsets their lower energy density. (1 mark) 6 MARKS

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EvaluateBand 5

8. Australia's transport sector is exploring ethanol (E10 blend, 10% ethanol by volume) as a fuel additive to petrol.

(a) Calculate ΔHc[ethanol] from ΔH°f data: C₂H₅OH(l) = −277.7; CO₂(g) = −393.5; H₂O(l) = −285.8 kJ mol⁻¹. Balanced equation: C₂H₅OH(l) + 3O₂(g) → 2CO₂(g) + 3H₂O(l). (3 marks)
(b) A car fuel tank holds 50 L of fuel. Petrol (octane, density 0.703 g mL⁻¹, M = 114.23 g mol⁻¹, ΔHc = −5471 kJ mol⁻¹) is compared with E10 (assume the ethanol component contributes 10% of volume and has density 0.789 g mL⁻¹). Estimate the energy difference (in MJ) from the ethanol component alone in a 50 L tank. (3 marks)
(c) The Australian government promotes E10 despite its lower energy density. Evaluate whether energy density alone is a valid basis for fuel policy decisions. (2 marks) 8 MARKS

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05

Revisit Your Thinking

Go back to your Think First prediction. The statement was: "A fuel with a larger ΔHc per mole always gives more energy per gram." Let's resolve it precisely:

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✅ Comprehensive Answers

🔬 Activity 1 — ΔH°f of Ethane

(a) 2C(graphite) + 3H₂(g) → C₂H₆(g) — formation equation producing exactly 1 mol C₂H₆ from elements in standard states.

(b) Scale (1) ×2: ΔH = −787.0; scale (2) ×3: ΔH = −857.4; reverse (3): ΔH = +1560.7. After cancellation: 2C + 3H₂ → C₂H₆ ✓. ΔH°f = −787.0 + (−857.4) + 1560.7 = −83.7 kJ mol⁻¹.

(c) ΣΔH°f(products) = 2(−393.5) + 3(−285.8) = −1644.4; ΣΔH°f(reactants) = −83.7. ΔHc = −1644.4 − (−83.7) = −1560.7 kJ mol⁻¹ — matches ΔH₃ ✓. Self-consistent cycle.

🔬 Activity 2 — Alcohol Fuel Comparison

(a) C₄H₉OH(l) + 6O₂(g) → 4CO₂(g) + 5H₂O(l). ΣΔH°f(p) = 4(−393.5) + 5(−285.8) = −3003.0; ΣΔH°f(r) = −327. ΔHc = −3003.0 − (−327) = −2676 kJ mol⁻¹.

(b) Methanol: 22.7 | Ethanol: 29.7 | Propan-1-ol: 33.6 | Butan-1-ol: 36.1 kJ g⁻¹. Trend: energy per gram increases with chain length — each CH₂ addition increases ΔHc faster than molar mass, approaching but never reaching alkane energy density.

❓ Multiple Choice

1. B — When ΔH°f data is provided, use the ΔH°f method — it is more accurate (experimental data, actual states) and directly applicable to the data given. The bond energy method is used only when ΔH°f data is unavailable.

2. A — Propane: 2220 ÷ 44.1 = 50.3 kJ g⁻¹; Butane: 2877 ÷ 58.1 = 49.5 kJ g⁻¹. Propane has slightly higher energy per gram. Option D demonstrates the exact misconception this lesson addresses.

3. B — The ΔH°f method uses experimentally measured values for each specific substance in its actual state at 25°C — the most accurate because no averaging is involved. Bond energy uses averages; Hess's Law accuracy depends on input quality.

4. C — ΣΔH°f(p) = 4(−393.5) + 5(−285.8) = −1574.0 − 1429.0 = −3003.0; ΣΔH°f(r) = 1(−126.2) + 0 = −126.2; ΔH = −3003.0 − (−126.2) = −3003.0 + 126.2 = −2876.8 ≈ −2877 kJ mol⁻¹. Option A uses the wrong formula direction (reactants − products).

5. A — The Hess's Law cycle via elements produces ΔHc = ΣΔH°f(products) − ΔH°f(fuel), which is exactly the ΔH°f formula. Both methods are mathematically identical — one is the cycle diagram representation and the other is the algebraic rearrangement of the same Hess's Law equation.

📝 Short Answer Model Answers

Q6 (6 marks):
(a) ΔH°f method gives −890.3 kJ mol⁻¹ — more accurate [½]. It uses experimentally measured values for each substance in its actual state (CO₂(g) and H₂O(l)) — not averages, and not assuming gaseous water [1½].
(b) Reason 1: The bond energy method assumed H₂O(g) as product (gaseous state assumption), but the actual product is H₂O(l) [1]. The condensation of 2 mol H₂O vapour → liquid releases an additional 2 × 44 ≈ 88 kJ mol⁻¹ of energy (latent heat) that is not counted in the bond energy result — this alone accounts for 88 of the 216 kJ mol⁻¹ discrepancy [1]. Reason 2: Bond energy values are averages across many molecular environments [1]. The C–H bond in methane, C=O bond in CO₂, and O–H bond in water each have slightly different actual values from the tabulated averages; these errors accumulate across 8 bond values in this calculation, introducing substantial total error [1].

Q7 (6 marks):
(a) ΣΔH°f(p) = 3(−393.5) + 4(−285.8) = −1180.5 + (−1143.2) = −2323.7 kJ mol⁻¹ [1]; ΣΔH°f(r) = 1(−303) + 9/2(0) = −303 kJ mol⁻¹ [1]; ΔHc = −2323.7 − (−303) = −2020.7 ≈ −2021 kJ mol⁻¹ ✓ [1].
(b) Propan-1-ol: 2021 ÷ 60.10 = 33.6 kJ g⁻¹ [1]; Butan-1-ol: 2676 ÷ 74.12 = 36.1 kJ g⁻¹ [1]. Butan-1-ol has higher energy density per gram [accept either in bold] [½]. Both are still below octane's 47.9 kJ g⁻¹ [½ credit for noting this].
(c) Any valid advantage — e.g. higher octane rating (reduces engine knock and allows higher compression ratios, improving efficiency) [1]; or renewable/carbon-neutral production cycle (produced from biomass); or reduced CO and particulate emissions; or improved oxygen content improves combustion completeness [1].

Q8 (8 marks):
(a) ΣΔH°f(p) = 2(−393.5) + 3(−285.8) = −787.0 + (−857.4) = −1644.4 kJ mol⁻¹ [1]; ΣΔH°f(r) = 1(−277.7) + 3(0) = −277.7 kJ mol⁻¹ [1]; ΔHc = −1644.4 − (−277.7) = −1366.7 ≈ −1367 kJ mol⁻¹ [1].
(b) Volume of ethanol = 10% × 50 L = 5 L = 5000 mL [½]. Mass(ethanol) = 5000 × 0.789 = 3945 g [½]. n(ethanol) = 3945 ÷ 46.07 = 85.6 mol [1]. Energy = 85.6 × 1367 = 117,000 kJ = 117 MJ [1].
(c) Energy density alone is not a valid sole basis for fuel policy [½]. Other critical factors include: (1) Renewability — ethanol from sugarcane is carbon-neutral over its lifecycle, unlike fossil fuels; reducing greenhouse gas emissions is a policy priority that outweighs the 3–4% reduction in fuel economy from E10 [1]. (2) Energy security — domestic fuel production reduces dependence on oil imports; for Australia, locally grown ethanol from sugarcane provides energy security benefits. (3) Environmental co-benefits — higher oxygen content in E10 reduces CO and hydrocarbon emissions, improving urban air quality [1]. Policy decisions require balancing multiple competing objectives, of which energy density is only one.

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Boss Battle

Hess's Law

Put your knowledge of Hess's Law to the test. Answer correctly to deal damage — get it wrong and the boss hits back. Pool: lessons 1–10.

Mark lesson as complete

Tick when you've finished all activities and checked your answers.