Hess’s law type 1

Some reactions’ enthalpy changes are difficult to measure, usually because they are very slow (e.g., iron rusting). Instead of measuring it directly, we can use Hess’s law.

The net changes in the properties of a system are independent of the way the system changes from the initial state to the final state. We can apply this like so: if a set of component reactions add up to equal a target reaction, then the components’ enthalpy changes must add up to equal the target’s enthalpy change:

`Delta H_"target" = sum Delta H_"known"`.

The enthalpy change symbols in this equation have subscripts, but they don’t represent molar enthalpies; they are measured in kJ, not kJ/mol.

Example

What is the enthalpy change for the formation of two moles of nitrogen monoxide given the following reference equations?

½ N2(g) + O2(g) → NO2(g), `Delta H_1 = 34\ "kJ"`

½ O2(g) + NO(g) → NO2(g), `Delta H_2 = -56\ "kJ"`

First, we should identify our target equation: N2(g) + O2(g) → 2 NO(g). We need one mole of N2 on the left side, so we need to multiply the first reference equation by 2. We need two moles of NO on the right side, so we must multiply the second equation by −2 (multiplying by a negative flips the equation). Remember to multiply the `Delta H` values as well.

N2(g) + 2 O2(g)2 NO2(g), `Delta H_1 = 68\ "kJ"`

2 NO2(g)O2(g) + 2 NO(g), `Delta H_2 = 112\ "kJ"`

When we add these, nitrogen dioxide and one mole of oxygen cancel out, leaving us with our target equation with the correct enthalpy change:

N2(g) + O2(g) → 2 NO(g), `Delta H = 180\ "kJ"`.