Molecularity in chemistry is the number of molecules that come together to react in an elementary reaction and is equal to the sum of stoichiometric coefficients of reactants in this elementary reaction. Depending on how many molecules come together, a reaction can be unimolecular, bimolecular or trimolecular.
In a unimolecular reaction, a single molecule rearranges atoms forming different molecules. This is illustrated by the equation
and is described by the first order rate law
where [A] is the concentration of species A, t is time, and kr is the reaction rate constant.
As can be deduced from the rate law equation, the number of A molecules that decay is proportional to the number of A molecules available. An example of a unimolecular reaction, is the isomerization of cyclopropane to propene:
Unimolecular reactions can be explained by the Lindemann-Hinshelwood mechanism.
In a bimolecular reaction, two molecules collide and exchange energy, atoms or groups of atoms.
This can be described by the equation
which corresponds to the second order rate law: d[A]/dt = -kr [A] [B].
Here, the rate of the reaction is proportional to the rate at which the reactants come together. An example of a bimolecular process, is the first step in binding of H2 and O2 to form water:
A termolecular reaction in solutions or gas mixtures involves three reactant molecules simultaneously colliding. However the term termolecular is also used to refer to three body association reactions of the type
Where the M over the arrow denotes that to conserve energy and momentum a second reaction with a third body is required. After the initial bimolecular collision of A and B an energetically excited reaction intermediate is formed, then, it collides with a M body, in a second bimolecular reaction, transferring the excess energy to it.
The reaction can be explained as two consecutive reactions:
These reactions frequently have a pressure and temperature dependence region of transition between second and third order kinetics.
Catalytic reactions are often three-component, but in practice a complex of the starting materials is first formed and the rate-determining step is the reaction of this complex into products, not an adventitious collision between the two species and the catalyst. For example, in hydrogenation with a metal catalyst, molecular dihydrogen first dissociates onto the metal surface into hydrogen atoms bound to the surface, and it is these monatomic hydrogens that react with the starting material, also previously adsorbed onto the surface.
Difference between molecularity and order of reaction
It is important to distinguish molecularity from order of reaction. The order of reaction is an empirical quantity determined by experiment from the rate law of the reaction. It is the sum of the exponents in the rate law equation. Molecularity, on the other hand, is deduced from the mechanism of an elementary reaction, and is used only in context of an elementary reaction. It is the number of molecules taking part in this reaction.
This difference can be illustrated on the reaction between nitric oxide and hydrogen:
The observed rate law is , so that the reaction is third order. Since the order does not equal the sum of reactant stoechiometric coefficients, the reaction must involve more than one step. The proposed two-step mechanism is
On the other hand, the molecularity of this reaction is undefined, because it involves a mechanism of more than one step. However, we can consider the molecularity of the individual elementary reactions that make up this mechanism:
The first step is termolecular because it involves three reactant molecules, while the second step is bimolecular because it involves two reactant molecules.
The kinetic order of any elementary reaction step is equal to its molecularity, and that the rate of an elementary reaction can therefore be determined by inspection, from the molecularity.
The kinetic order of a complex reaction; however, cannot be equated to molecularity since molecularity only describes elementary reactions.
- Atkins, P.; de Paula, J. Physical Chemistry. Oxford University Press, 2014
- Temkin, O. N. State-of-the-Art in the Theory of Kinetics of Complex Reactions. In Homogeneous Catalysis with Metal Complexes: Kinetic Aspects and Mechanisms, John Wiley and Sons, ltd, 2012
- J.I. Steinfeld, J.S. Francisco and W.L. Hase Chemical Kinetics and Dynamics (2nd ed., Prentice Hall 1999) p.5, ISBN 0-13-737123-3
- Text discussing rate constants for termolecular reactions 
- IUPAC definition of Troe expression, a semiempirical expression for the rate constant of termolecular reactions 
- Carr, R. W. Chemical Kinetics. In Encyclopedia of Applied Physics. WILEY-VCH Verlag GmbH & Co KGaA, 2003
- Rogers, D. W. Chemical Kinetics. In Concise Physical Chemistry, John Wiley and Sons, Inc. 2010.
- Keith J. Laidler, Chemical Kinetics (2nd ed., McGraw-Hill 1965), p.321–2