For a reaction to be spontaneous only at high temperatures, the enthalpy change (\(\Delta_r H^\circ\)) must be positive, indicating that the reaction absorbs heat. Additionally, the entropy change (\(\Delta_r S^\circ\)) must also be positive, meaning the disorder of the system increases.
These factors influence the Gibbs free energy equation: \[ \Delta_r G^\circ = \Delta_r H^\circ - T\Delta_r S^\circ \] As the temperature \(T\) increases, the term \(T\Delta_r S^\circ\), which is subtracted from \(\Delta_r H^\circ\), becomes significant enough to make \(\Delta_r G^\circ\) negative, hence driving the reaction to spontaneity at higher temperatures.
The speed at which a chemical reaction takes place is called the rate of reaction. The rate of reaction depends on various factors like concentration of the reactants, temperature, etc. The relation between the rate of reaction and the concentration of reacting species is represented by the equation \( r = k[A]^x[B]^y \), where \( x \) and \( y \) are the order of the reaction with respect to the reactants A and B, respectively. The overall order of the reaction is \( x + y \). The rate of reaction can also be increased by the use of a catalyst which provides an alternate pathway of lower activation energy. It increases the rate of forward and backward reactions to an equal extent. It does not alter the Gibbs energy of the reaction.