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*Revision Materials and Past Papers* 2.1.1 Atomic structure and isotopes 2.1.2 Compounds, formulae and equations 2.1.3 Amount of substance 2.1.4 Acids 2.1.5 Redox 2.2.1 Electron structure 2.2.2 Bonding and structure 3.1.1 Periodicity 3.1.2 Group 2 3.1.3 The halogens 3.1.4 Qualitative analysis 3.2.1 Enthalpy 3.2.2 Reaction Rates 3.2.3 Chemical equilibrium 4.1 Basic concepts and hydrocarbons 4.1.2 Alkanes 4.1.3 Alkenes 4.2.1 Alcohols 4.2.2 Haloalkanes 4.2.3 Organic synthesis 4.2.4 Analytical techniques 5.1.1 How fast? 5.1.2 How far? 5.1.3 Acids, bases and buffers 5.2.1 Lattice enthalpy 5.2.2 Enthalpy and entropy 5.2.3 Redox and electrode potentials 5.3.1 Transition elements 5.3.2 Qualitative analysis 6.1.1 Aromatic compounds 6.1.2 Carbonyl compounds 6.1.3 Carboxylic acids and esters 6.2.1 Amines 6.2.2 Amino acids, amides and chirality 6.2.3 Polyesters and polyamides 6.2.4 Carbon–carbon bond formation 6.2.5 Organic synthesis 6.3.1 Chromatography and qualitative analysis 6.3.2 Spectroscopy Required Practicals

3.2.1 Enthalpy

Bond enthalpiesEnthalpy changesHess’ law and enthalpy cycles

Enthalpy Changes

Specification Reference 3.2.1 (a)–(h)

Quick Notes

  • Enthalpy Change (ΔH) is heat change at constant pressure.
    • Exothermic: ΔH is negative and energy released (e.g. combustion).
    • Endothermic: ΔH is positive and energy absorbed (e.g. bond breaking).
  • Enthalpy Level Diagrams show energy level of reactants vs products:
    • Exothermic: products lower than reactants.
    • Endothermic: products higher than reactants.
  • Activation Energy (Ea): minimum energy needed for a reaction to occur. Appears as a ‘hump’ in energy profile diagrams.
  • Standard conditions: 100 kPa, 298 K, substances in standard states.
  • Standard Enthalpy Changes:
    • Standard Enthalpy of Reaction, ΔrH:
      Enthalpy change when reactants react in the molar quantities given in the reaction equation.
    • Standard Enthalpy of Formation, ΔfH:
      Enthalpy change of formation (1 mol compound from elements).
    • Standard Enthalpy of Combustion, ΔcH:
      Enthalpy change of combustion (1 mol burned completely in O2).
    • Standard Enthalpy of Neutralisation,ΔneutH:
      Enthalpy change of neutralisation (1 mol water formed).
  • Formulas for calculations:
    • q = mcΔT
      • q = energy (J), m = mass (g), c = specific heat capacity (4.18 J g⁻¹ K⁻¹), ΔT = temp change (K).
    • ΔH = q / n
      • where n = moles of the limiting reactant.

Full Notes

Enthalpy change (ΔH) is the heat change during a chemical reaction at constant pressure.

Exothermic reactions release heat (ΔH is negative).
For Example: Combustion of fuels.

Endothermic reactions absorb heat (ΔH is positive).
For Example: Thermal decomposition reactions.

Enthalpy Level Diagrams

Enthalpy level diagrams shows the enthalpies of reactants and products for a given reaction:

Exothermic: products lie below reactants.

OCR (A) A-Level Chemistry diagram of exothermic enthalpy level with products below reactants.

Endothermic: products lie above reactants.

OCR (A) A-Level Chemistry diagram of endothermic enthalpy level with products above reactants.

The vertical difference = ΔH.

Note: These diagrams do not show activation energy, only the net enthalpy change. Reaction profile diagrams show activation energy.

Activation Energy (Ea)

Activation energy (Ea) is the minimum amount of energy required to initiate a reaction.

OCR (A) A-Level Chemistry reaction profile diagram showing activation energy hump.

On an reaction profile diagram, it’s the energy ‘hump’ between reactants and the highest energy reached in the reaction.

Standard Enthalpy Terms

Standard conditions: 100 kPa, 298 K, and standard states.
All ΔH values refer to 1 mole.

Calculating Enthalpy Changes from Experiments

Calorimetry is an experimental technique used to measure enthalpy changes.

The key equation is:

q = mcΔT

where:
q = heat energy change (J)
m = mass of substance heated (g)
c = specific heat capacity (J g⁻¹ K⁻¹) (for water, c = 4.18 J g⁻¹ K⁻¹)
ΔT = temperature change (K)

The enthalpy change per mole of reactant can now be calculated using:

ΔH = -q / n

where n = moles of the limiting reactant.

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Matt’s exam tip

Remember the m in q = mcΔT refers to the mass of surroundings, not the mass of reactants used. You need the mass of reactants only to find moles (n) for ΔH.


Worked Example

Ethanol (C2H5OH) burns in oxygen:
C2H5OH + 3O2 → 2CO2 + 3H2O

  1. A student burns 0.5 g of ethanol and heats 100 g of water by 20°C.
  2. Calculate q:
    q = mcΔT = 100 × 4.18 × 20 = 8360 J = 8.36 kJ
  3. Find moles of ethanol burned:
    Molar mass = 46 g mol⁻¹
    Moles = 0.5 ÷ 46 = 0.01087 mol
  4. Calculate ΔHc:
    ΔH = q ÷ n = 8.36 ÷ 0.01087 = −769 kJ mol⁻¹

Final Answer: ΔHc = −769 kJ mol⁻¹ (exothermic)

Summary