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S1.1 - Introduction to the particulate nature of matter S1.2 - The nuclear atom S1.3 - Electron configurations S1.4 - Counting particles by mass - The mole S1.5 - Ideal gases S2.1 - The ionic model S2.2 - The covalent model S2.3 - The metallic model S2.4 - From models to materials S3.1 - The periodic table - Classification of elements S3.2 - Functional groups - Classification of organic compounds R1.1 - Measuring enthalpy changes R1.2 - Energy cycles in reactions R1.3 - Energy from fuels R1.4 - Entropy and spontaneity AHL R2.1 - How much? The amount of chemical change R2.2 - How fast? The rate of chemical change R2.3 - How far? The extent of chemical change R3.1 - Proton transfer reactions R3.2 - Electron transfer reactions R3.3 - Electron sharing reactions R3.4 - Electron-pair sharing reactions

R2.2 - How fast? The rate of chemical change

2.2.1 Rate of Reaction 2.2.2 Collision Theory 2.2.3 Factors Affecting Reaction Rate 2.2.4 Activation Energy and Temperature 2.2.5 Catalyst and Activation Energy 2.2.6 Reaction Mechanism and Intermediates (AHL) 2.2.7 Energy Profile and Rate Determining Step (AHL) 2.2.8 Molecularity in Reaction Mechanism (AHL) 2.2.9 Rate Equations and Experimental Data (AHL) 2.2.10 Reaction Orders and Graphs (AHL) 2.2.11 Rate Constant, K (AHL) 2.2.12 Arrhenius Reaction and Temperature (AHL) 2.2.13 Arrhenius Factor and Activation Energy (AHL)

The Rate Constant, k and Its Units HL Only

Specification Reference R2.2.11

Quick Notes

  • The rate constant (k) links rate and concentration in the rate equation: rate = k[A]m[B]n.
  • The value of k is specific to a reaction and increases with temperature.
  • Units of k depend on the overall order of the reaction.
  • Units can be determined by rearranging the rate equation using:
    • Rate units = mol dm⁻³ s⁻¹
    • Concentration units = mol dm⁻³

Full Notes

What Is the Rate Constant, k?

The rate constant (k) appears in the rate equation for a reaction and reflects how temperature, activation energy, and collision orientation influence the reaction rate.

Temperature dependence: as temperature increases, more particles overcome the activation barrier, so k increases.

Rate Equation and Units of k

A rate equation (also called a rate law) takes the general form:

rate = k[A]m[B]n

Units of k vary depending on the overall order of the reaction:

Worked Example

Determine the units of k if a reaction is first order in A and second order in B.

  1. Rate law: rate = k[A][B]²
  2. Units:
    • rate = mol dm⁻³ s⁻¹
    • [A] = mol dm⁻³
    • [B]² = (mol dm⁻³)² = mol² dm⁻⁶
  3. Solve for k:
    k = rate / ([A][B]²)
    Units = (mol dm⁻³ s⁻¹) / (mol dm⁻³ × mol² dm⁻⁶) = mol⁻² dm⁶ s⁻¹

Summary

Linked Course Question

Reactivity 3.4 – Linked Course Question

What are the rate equations and units of k for the reactions of primary and tertiary halogenoalkanes with aqueous alkali?

Primary halogenoalkanes follow an SN2 mechanism (bimolecular): Rate = k[halogenoalkane][OH⁻]. Overall order = 2. Units of k: mol⁻¹ dm³ s⁻¹.

Tertiary halogenoalkanes follow an SN1 mechanism (unimolecular): Rate = k[halogenoalkane]. Overall order = 1. Units of k: s⁻¹.

The different rate laws reflect the different mechanisms and species involved in the rate-determining step.