The standard enthalpy change of reaction ΔHr is the enthalpy change that accompanies a reaction in the molar quantities expressed in a chemical equation under standard conditions, all reactants and products being in their standard states.
The standard enthalpy change of combustion ΔHc is the enthalpy change that takes place when one mole of a substance reacts completely with oxygen under standard conditions, all reactants and
products being in their standard states.
C2H6(g) + 3½ O2 (g) --> 2CO2(g) + 3H2O(l)
The standard enthalpy change of formation ΔHf is the enthalpy change that takes place when one mole of a compound is formed from its constituent elements in their standard states under standard conditions.
H2(g) + ½ O2 (g) --> H2O(l) ΔHf = -286kJmol-1
Sum (bonds broken) – Sum (bonds made) =Energy change
activation energy is the energy needed to start the
reaction by breaking chemical bonds in the
reactants. Energy is given out when new
chemical bonds form.
The overall energy change for a reaction can be
worked out as the energy required for all bonds
broken minus the energy gained by making bonds.
How does calorimetry work?
A known volume of cold water is measured
into the beaker/can
The starting temperature of the water is
recorded
The water is heated using the flame from the
burning fuel
The final temperature of the water is recorded
The spirit burner containing the fuel is
weighed before and after the experiment.
ΔE = mcΔT
Energy transferred (joules, J) = mass of water
heated × 4.2 × temperature rise
reasons for errors in calorimetry
Energy lost to the surroundings
Incomplete combustion
Conditions which are not standard (ie not 298K and 1atm pressure)
Hess’ law states that - if a reaction can take place by
more than one route and the initial and final
conditions are the same, the total enthalpy change