1.2.2—Hess's law
- Syllabus
- First assessment 2025
- Objective
- 1.2.2
- Level
- SL
Hess's law states that enthalpy change is independent of reaction pathway. Enthalpy values can therefore be combined through a balanced cycle.
Reverse an entire balanced equation by changing the sign of ΔH; scale every coefficient and ΔH by the same factor; then add equations and cancel identical species in identical physical states. Never change a chemical subscript, formula or state symbol merely to force cancellation. The surviving equation must exactly match the target before enthalpies are summed.
Treat chemical equations like algebra: reverse a step and reverse its ΔH sign; multiply all coefficients and ΔH by the same factor; then add and cancel species. The surviving overall equation must exactly match the target before the enthalpies are summed.
Worked example — Hess's law: target C(s)X2+HX2(g)X1+/2OX2(g)CHX3OH(l). Use CX+OX2COX2, ΔH=−394kJmol−1; double HX2X+1/2OX2HX2O(l) to give −572kJmol−1; reverse methanol combustion to give +726kJmol−1. After cancelling COX2 and HX2O, ΔH=−394−572+726=−240kJmol−1 for the target equation.
Representative question
Determine the enthalpy change, ΔH, in kJmol−1, for the hydration of solid anhydrous magnesium sulfate, MgSO4.
ΔH(=ΔH1−ΔH2)=−99( kJ mol−1);
Marking guidance:
Award [1] if -86 is used giving an answer of −104( kJ mol−1).
Retrieve the route: count bond breaking/forming, manipulate Hess equations, define standard formation/combustion values, apply product–reactant sums, and track every Born–Haber energy term.
Check equation direction, coefficients, signs, standard states, lattice enthalpy convention, and one-versus-two-electron steps.