The Gibbs-Helmholtz equation describes the temperature dependence of the Gibbs free energy (\(G\)) or the Gibbs free energy change (\(\Delta G\)) of a system or process.
One common form is:
$$ \left( \frac{\partial (\Delta G / T)}{\partial T} \right)_P = -\frac{\Delta H}{T^2} $$
Another form relates the change in \(\Delta G\) with temperature directly to the enthalpy change (\(\Delta H\)):
$$ \Delta G = \Delta H + T \left( \frac{\partial (\Delta G)}{\partial T} \right)_P $$
These equations show how \(\Delta G\) varies with temperature, connecting it explicitly to the enthalpy change (\(\Delta H\)) of the process.
While \(\Delta G\) itself predicts reaction direction (spontaneity) (Option 1), and its relation to the equilibrium constant \(K\) (\(\Delta G^\circ = -RT \ln K\)) allows calculation of K (partly related to Option 3, via temperature), the *specific significance* of the Gibbs-Helmholtz equation is its description of the *temperature dependence* of \(\Delta G\) and its direct link to \(\Delta H\).
Option (2) best captures this significance.
Option (4) is incorrect.