Standard Enthalpy of Reactions
If enthalpy of reactants is denoted as Hreactants and total enthalpy of products as Hproducts, the difference between these enthalpies, is the enthalpy of the reaction
ΔrH = Hproducts – Hreactants
When Hproducts is greater than Hreactants then ΔH is positive and heat is absorbed in the reaction, and the reaction is endothermic. For example,
H2 (g) + I2 (g) → 2HI (g); ΔrH = 52.5 kJ
When Hproducts is less than Hreactants then H is negative and heat is evolved in the reaction, and the reaction is exothermic. For example,
CH4 (g) + 2O2 (g) → CO2 (g) + 2H2O (l); ΔrH = –890.4 kJ
Enthalpy of Formation
The enthalpy change when one mole of a pure compound is formed from its elements in their most stable states is called the enthalpy of formation and is denoted by ΔfH0.
For example:
C(Graphite) + O2 (g) → CO2 (g) ; ΔfH0 = –393.5 kJ mol–1
Enthalpy of Combustion
Enthalpy of combustion is the enthalpy change (heat evolved) accompanying the complete combustion of 1 mole of a substance in oxygen at a given temperature and 1 bar pressure.
For example:
C2H5OH (l) + 3O2 (g) → 2CO2 (g) + 3H2O (l) ; ΔcombH0 = –1365.6 kJ
Enthalpy of Neutralization
Enthalpy of neutralization isthe enthalpy change (heat evolved) when one mole of hydrogen ions (H+) is neutralized by one mole of hydroxyl ions (OH-) in dilute aqueous medium to form water.
For example:
H+ (aq) + OH– (aq) → H2O (l) ; ΔneutH0 = –57 kJ/mol