Activation Energy and Spontaneous reactions

Even if a reaction is classified as spontaneous thermodynamically (i.e. ΔG<0) it may not start due to a high activation energy (kinetic barrier).

This is the case for the reaction of diamond with oxygen for example. Similarly, the breaking of the N-N triple bond and the H-H single bond in the Haber process are spontaneous at high temperature but too slow to be economically useful. In fact all reactions which use a catalyst do so in order to overcome the activation energy (Ea).

For combustion and other very exothermic reactions only a few particles need to overcome the activation barrier in order to provoke a runaway effect, with energy released supplying the Ea for further reaction:
 

 

     
 
Don't be deceived into thinking activation energy is extra energy which affects enthalpy changes. Whatever energy is lost in getting to the transition state is gained going down the other side to the products. Activation energy has no net effect on enthalpy change of reaction
/ activated complex Runaway effect
Please note that the moving dot does not represent a particle but the progress of the reaction.

The changing height represents the relative energy of the reactants and products
.

Clearly, products will have greater thermal (kinetic) energy which they will pass on through collisions to more reactants.