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R1.2.3 Standard enthalpy changes of combustion and formation (Higher Level Only)

Standard Enthalpy of Combustion (ΔHc) and Formation (ΔHf)

Standard Enthalpy of Combustion (ΔHc)

Definition

Standard enthalpy of combustion

The standard enthalpy of combustion (ΔHc) is the energy change when one mole of a substance is completely burned in oxygen under standard conditions (298 K and 1 atm).

The products of combustion must also be in their standard states (e.g., CO₂ as a gas and H₂O as a liquid).

Example

The combustion of methane (CH₄) is represented as:

CH4(g)+2O2(g)CO2(g)+2H2O(l)ΔHc=890kJ mol1

This equation tells us that burning 1 mole of methane releases 890 kJ of energy.

Key Features of ΔHc

  • Exothermic Nature: Combustion reactions are always exothermic, meaning ΔHc values are negative because energy is released to the surroundings.
  • Standard States: All reactants and products must be in their standard states.

Example

Oxygen is a gas (O₂(g)), and water is a liquid (H₂O(l)) at standard conditions.

  • Applications: ΔHc values are essential for comparing the energy efficiency of different fuels, such as coal, gasoline, and hydrogen.

Example

Combustion of Butane

The combustion of butane (C₄H₁₀), a fuel commonly used in lighters, is represented as:

C4H10(g)+132O2(g)4CO2(g)+5H2O(l)ΔHc=2878kJ mol1

This means burning 1 mole of butane releases 2878 kJ of energy.

Tip

ΔHc values for common substances are listed in Section 14 of the IB Chemistry Data Booklet. Use these values for accurate calculations.

Standard Enthalpy of Formation (ΔHf)

Definition

Standard enthalpy of formation

The standard enthalpy of formation (ΔHf) is the energy change when one mole of a compound is formed from its elements in their standard states under standard conditions.

Example

The formation of water (H₂O) from hydrogen and oxygen is:

H2(g)+12O2(g)H2O(l)ΔHf=286kJ mol1

This means that forming 1 mole of liquid water from hydrogen gas and oxygen gas releases 286 kJ of energy.

Key Features of ΔHf

  • Reference Point: The ΔHf of any element in its standard state is zero.

Example

  • ΔHf of O₂(g) = 0
  • ΔHf of C(s, graphite) = 0
  • Exothermic or Endothermic: Formation reactions can be either exothermic (negative ΔHf) or endothermic (positive ΔHf), depending on the compound.
  • Applications: ΔHf values are used to calculate reaction enthalpy changes using Hess’s law.

Example

Formation of Methane

The formation of methane (CH₄) from carbon and hydrogen is represented as:

C(s)+2H2(g)CH4(g)ΔHf=74.8kJ mol1

This means forming 1 mole of methane releases 74.8 kJ of energy.

Note

ΔHf values for many compounds are listed in Section 13 of the IB Chemistry Data Booklet.

Reflection

Theory of Knowledge

How does the use of models (like ΔHc and ΔHf) in chemistry help us understand energy changes? What are the limitations of these models in predicting real-world behavior?

Self review

Can you calculate the enthalpy change for a reaction using ΔHf values? What about using ΔHc values? Practice solving a problem from your data booklet to reinforce your understanding.

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Questions

Recap questions

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Question 1

Given the combustion reaction of butane, calculate the total energy released when 2 moles of butane are burned. Use the provided ΔHcθΔH_c^\theta value for butane.

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What are the standard conditions for measuring enthalpy changes?

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Note

Introduction to Enthalpy Change

  • Enthalpy change is the heat energy change measured at constant pressure.
  • It is represented by the symbol ΔH\Delta H .
  • Standard conditions for measuring enthalpy change are:
    • Temperature: 298 K (25°C)
    • Pressure: 1 atm (101.3 kPa)
    • Concentration: 1 mol dm-3 (for solutions)
  • Elements and compounds are in their standard states
    under these conditions.

Analogy

Think of standard conditions like the default settings on a computer - they provide a common reference point for comparison.

Example

Oxygen's standard state is O₂(g) while water's standard state is H₂O(l) at 298 K and 1 atm.