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Enthalpy change
H°, heat energy change of a reaction
Standard conditions
100 kPa pressure, usually 298 K temperature
Standard states
Physical states of reactants under standard conditions
Bond breaking vs making
Energy taken in to break bonds, energy released when making bonds
Endothermic reaction
More energy needed to break bonds than to make, ΔH positive, heat absorbed
Exothermic reaction
More energy released in making bonds than breaking, ΔH negative, heat released
Overall enthalpy change
ΔH = energy to break bonds (+) + energy released by making bonds (-)
Activation energy
Ea, minimum energy required for a reaction to occur between colliding particles
Enthalpy profile diagram
Shows energy changes during a reaction, with Ea as the peak above reactants
Enthalpy change of reaction
ΔH°, enthalpy change for a stated reaction under standard conditions
Enthalpy change of formation
ΔHf°, enthalpy change when 1 mole of a substance is formed from elements in standard states
Enthalpy change of combustion
ΔHc°, enthalpy change when 1 mole of a substance is completely burned in oxygen
Enthalpy change of neutralisation
ΔHneut°, enthalpy change when 1 mole of water is formed from acid and alkali under standard conditions
Calorimetry
Method to determine enthalpy change by measuring temperature change over time
Energy change formula
q = m × c × ΔT
Variables in calorimetry
q = energy change (J), m = mass (g), c = specific heat capacity (J g⁻¹ K⁻¹), ΔT = temperature change (K)
Specific heat capacity
Energy required to raise 1 g of substance by 1 K without change of state
Calculating ΔH per mole
ΔH = (q × 10⁻³) ÷ moles
Sources of error in calorimetry
Heat loss by conduction or convection, inaccurate temperature measurement
Minimising heat loss
Lid on calorimeter, insulation like polystyrene
Assumptions in calorimetry
Specific heat capacity taken as 4.18 J g⁻¹ K⁻¹, calorimeter heat capacity ignored