The term standard state is used to describe a reference state for substances, and is a help in thermodynamical calculations (as enthalpy, entropy and Gibbs free energy calculations). The superscript degree symbol (°) indicates that substances are in their standard states. (ΔH°, ΔG°, S°. )
Definitions of standard states:
Note! Standard state is NOT the same as standard temperature and pressure (STP) for a gas, and must not be confused with this term.
Enthalpy is a state function, defined by the internal energy (E), the pressure (P) and volume (V) of a system:
H = E + PV and ΔH = ΔE + Δ(PV)
For enthalpy, there are no method to determine absolute values, only enthalpy changes (ΔH values) can be measured. Then it is important to have a common and well defined reference state. Since enthalpy is a state function, a change in enthalpy does not depend on the pathway between two states.
Hess's law: In going from a particular set of reactants to a particular set of products, the change in enthalpy is the same whether the reaction takes place in one step or in a series of steps.
At constant pressure: ΔH = qp (qp = heat from or to the chemical system at constant pressure, q is also called heat of reaction)
Exothermic reaction: negative ΔH (heat transferred to the surroundings from the system)
Endothermic reaction: positive ΔH (heat adsorbed by the system from the surroundings)
The standard enthalpy of formation (ΔH 0 f) of a compound is the change in enthalpy that accompanies the formation of 1 mole of a compound from its elements with all substances in their standard states.
The table below shows the standard enthalpy of formation, the standard Gibbs free energy of formation, standard entropy and molar heat capacity at constant pressure of several inorganic compounds.
The specific heat capacity can be calculated from the molar heat capacity, and vise versa:
cp = specific heat capacity
M = molar weight of the actual substance (g/mol).