Grades/ Grade 11/ Chemistry/ Chemical Kinetics/Lecture
Class XI · Chemistry · Unit 9

Chemical Kinetics — the full lecture.

Reaction rate, the factors that change it, the rate law & order, collision theory, activation energy and catalysis — exam-focused for the BIEK / Sindh Board paper. Read it, or open the interactive lecture and drive the rate simulator.

🌍 In the real world — Reaction rates shape daily life: we chill food in a fridge to slow spoiling, a catalytic converter cleans car exhaust, fine dust can explode, and a pressure cooker's heat cooks food in half the time.
  • Rate of reaction — the change in concentration of a reactant or product per unit time. Unit: mol dm⁻³ s⁻¹.
Raterate = − Δ[reactant]/Δt = + Δ[product]/Δt

The rate is fastest at the start (most reactant) and slows as reactants are used up.

FactorEffect (increase →)
Concentration (of reactant)faster — more collisions
Temperaturemuch faster — more energetic & frequent collisions
Surface area (solid)faster — more contact
Catalystfaster — lowers activation energy
Pressure (gases)faster — molecules closer
Nature of reactants / lightvaries
For aA + bB → productsrate = k [A]ᵐ [B]ⁿ
k = rate constant · m, n = orders (found by experiment)

The rate constant k is independent of concentration but increases with temperature. Its units depend on the overall order.

  • Order — the power to which a reactant's concentration is raised in the rate law. Overall order = m + n. It is found experimentally, not from the equation.
OrderRateUnits of k
zerorate = kmol dm⁻³ s⁻¹
firstrate = k[A]s⁻¹
secondrate = k[A]²mol⁻¹ dm³ s⁻¹
MolecularityOrder
number of species in one elementary stepexperimental power in the rate law
always a whole number (1, 2, 3)can be 0, fractional, or whole
theoretical (for a step)determined by experiment
The slowest step in a mechanism is the rate-determining step — it controls the overall rate.

For a reaction to occur, particles must collide. But not every collision reacts — an effective collision needs:

  • enough energy (≥ the activation energy, Ea), and
  • the correct orientation.

Anything that increases the frequency or energy of collisions increases the rate.

  • Activation energy (Ea) — the minimum energy colliding particles must have to react.
  • Activated complex (transition state) — the high-energy, unstable arrangement at the top of the energy barrier.

On an energy profile, reactants climb the Ea barrier to the transition state, then fall to products. Exothermic: products lower than reactants; endothermic: higher.

A rise of ~10 °C roughly doubles the rate. Higher temperature gives molecules more kinetic energy, so a much larger fraction have energy ≥ Ea (the Maxwell–Boltzmann distribution shifts right).

Arrhenius equationk = A e^(−Ea/RT)
A = frequency factor · R = gas constant · T = kelvin
  • Catalyst — a substance that speeds up a reaction by providing an alternative path with a lower activation energy, and is not used up itself.
TypeDescriptionExample
Homogeneoussame phase as reactantsacid in ester hydrolysis
Heterogeneousdifferent phase (usually solid)Fe in Haber, Pt in catalytic converters
A catalyst lowers Ea for both directions equally — it speeds up the approach to equilibrium but does not change the position or K.
  • Measure a gas volume produced over time (e.g. CO₂, H₂).
  • Measure mass loss (gas escaping) on a balance.
  • Measure colour / light absorbed (colorimetry).
  • Measure conductivity or pH if ions change.
  • Time how long a precipitate takes to obscure a mark.
order from data
When [A] doubles, the rate doubles. What is the order in A?
rate ∝ [A]¹ → first order
rate constant
A first-order reaction has rate = 4×10⁻³ mol dm⁻³ s⁻¹ when [A] = 0.2 M. Find k.
k = rate/[A] = (4×10⁻³)/0.2 = 0.02 s⁻¹
temperature
If a reaction's rate doubles per 10 °C, how much faster is it 30 °C hotter?
2 × 2 × 2 = 8 times faster
  1. Rate definition & units; rate is fastest at the start.
  2. Factors: concentration, temperature, surface area, catalyst.
  3. Rate law rate = k[A]ᵐ[B]ⁿ; order & rate constant.
  4. Molecularity vs order; rate-determining step.
  5. Collision theory; activation energy & energy profile.
  6. Arrhenius (temperature); how a catalyst lowers Ea.
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