Chapter 27. Molecular Reaction Dynamics

1. Chapter 27. Molecular Reaction Dynamics Purpose: Calculation of rate constants for simple elementary reactions. For reactions to take place: 1. Reactant molecules must meet. 2. Must hold a minimum energy. Gas phase reactions: Collision theory. Solution phase reactions: Diffusion controlled. Activation controlled.

2. 27.1 Collision theory • Consider a bimolecular elementary reaction A + B → P v = k2[A][B] The rate of v is proportional to the rate of collision, and therefore to the mean speed of the molecules, • Because a collision will be successful only if the kinetic energy exceeds a minimum value. It thus suggests that the rate constant should also be proportional to a Boltzmann factor of the form, . • Consider the steric factor, P, • Therefore, k2 is proportional to the product of steric requirement x encounter rate x minimum energy requirement

3. Collision rate in gases • Collision density, ZAB, is the number of (A, B) collisions in a region of the sample in an interval of time divided by the volume of the region and the duration of the interval. where σ = d2 d = ½(dA + dB) and u is the reduced mass • when A and B are the same, one gets • The collision density for nitrogen at room temperature and pressure, with d = 280 pm, Z = 5 x 1034 m-3s-1.

4. The energy requirement • For a collision with a specific relative speed of approach vrel • reorganize the rate constant as • Assuming that the reactive collision cross-section is zero below εa

6. The steric effect • Steric factor, P, • Reactive cross-section, σ*, • σ* = P σ • Harpoon mechanism: Electron transfer preceded the atom extraction. It extends the cross-section for the reactive encounter. • K and Br2 reaction

7. Example 27.1 Estimate the steric factor for the reaction H2 + C2H4 -> C2H6 at 628K given that the pre-exponential factor is 1.24 x 106 L mol-1 s-1. Solution: Calculate the reduced mass of the colliding pair From Table 24.1 σ(H2) = 0.27 nm2 and σ(C2H4) = 0.64 nm2, given a mean collision cross-section of σ = 0.46 nm2. P = 1.24 x 106 L mol-1 s-1/7.37 x 1011 L mol-1s-1 = 1.7 x 10-6

8. Example 27.2: Estimate the steric factor for the reaction: K + Br2→ KBr + Br Solution: The above reaction involves electron flip K + Br2→ K+ + Br2- Three types of energies are involved in the above process: (1) Ionization energy of K, I (2) Electron affinity of Br2, Eea (3) Coulombic interaction energy: Electron flip occurs when the sum of the above three energies changes sign from positive to negative

9. 27.2 Diffusion-controlled reactions • Cage effect: The lingering of one molecule near another on account of the hindering presence of solvent molecules. • Classes of reaction Suppose that the rate of formation of an encounter pair AB is first-order in each of the reactants A and B: A + B →AB v = kd[A][B] The encounter pair, AB, has the following two fates: AB → A + B v = kd’[AB] AB → P v = ka[AB] • The net rate of change of [AB]: = kd[A][B] - kd’[AB] - ka[AB]

10. Invoking steady-state approximation to [AB] • The net rate of the production: • When kd’<< ka k2 = kd (This is diffusion-controlled limit) • When kd’>> ka (This is activation-controlled reaction)

11. Reaction and Diffusion • where R* is the distance between the reactant molecules and D is the sum of the diffusion coefficients of the two reactant species. where η is the viscosity of the medium. RA and RB are the hydrodynamic radius of A and B. • If we assume RA = RB = 1/2R*

12. 27.3 The material balance equation (a) The formulation of the equation the net rate of change due to chemical reactions the over rate of change the above equation is called the material balance equation.

13. (b) Solutions of the equation

14. 27.4 The Eyring equation • The transition state theory pictures a reaction between A and B as proceeding through the formation of an activated complex in a pre-equilibrium: A + B -> C‡ K‡ = ( `‡` is represented by `±` in the math style) • The partial pressure and the molar concentration has the following relationship: pJ = RT[J] • thus [C‡] = K‡ [A][B] • The activated complex falls apart by unimolecular decay into products, P, C‡ → P v = k‡[C‡] • So v = k‡ K‡ [A][B] Define k2 = k‡ K‡ v = k2[A][B]