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Reaction kinetics play a vital role in establishing the mechanism of a chemical reaction, and aiding the design of suitable equipment, such as reactors, as well as informing the operating conditions and control methods of such machinery. This lesson will introduce the concepts used to achieve this.

Reaction Order and Molecularity

The classification of a reaction is based on the reaction kinetics, where a reaction can be one of four mechanisms:

  • Irreversible
  • Reversible
  • Simultaneous
  • Consecutive

This classification is related to the reaction order, which can be related to the molecularity of the reaction. The molecularity is the number of molecules coming together to react in an elementary reaction. The reaction order is sometimes identical to the molecularity, but in other terms may be a zero order reaction, where the rate of reaction does not vary with concentration. The Power Law Rate Equation shown in Equation 1 is used to determine the reaction order, where the sum of the exponents for each reactant concentration is the reaction order.

\(r = k C^p_a C^q_b\)

Equation 1. Power Law Rate Equation, where \(r\) is the reaction rate, \(k\) is the rate constant, \(C_a\) is the concentration of a Reactant ‘A’, \(p\) is the reaction order with respect to Reactant ‘A’, \(C_b\)is the concentration of a Reactant ‘B’, and \(q\) is the reaction order with respect to Reactant ‘B’.

The half life (\(t_{1/2}\)) is the time taken for the quantity of a substance to decay to half of its original amount. For first order and second order reactions, the relationship between an initial concentration of a substance (e.g. \([A]_0\)) is relatively simple. The derivation for both first in Equation 2.

\(- \frac{d[A]}{dt} = k[A]\)

\(\int_{[A]_0}^{[A]} \frac{1}{[A]} d[A] = -\int_{0}^{t} k dt\)

\(ln(\frac{[A]}{[A]_0}) = -kt\)

\(\text{At} \: t_{1/2} \: [A] = \frac{[A]_0}{2}\)

\(\text{Thus} \: ln(2) = kt_{1/2}\)

Equation 2. Derivation of half-life (\(t_{1/2}\)) for a first order reactant in relation to the rate constant (\(k\)). \([A]\) represents the concentration of a Reactant ‘A’ at a time ‘t’, where \([A]_0\) is the concentration of Reactant ‘A’ when \(t=0\).

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