Skip to content
Dabour HubLEARN · PRACTICE · EXPLORESign inStudent

2.5.7Inorganic Chemistry

Transition Metal Catalysts — Oxford AQA International A Level Chemistry Revision Notes & Topical Questions

5 min read 5 parts Lesson 24 of 27

🩺
100% Curriculum Specification Match Lesson Doctor Verified
The only platform with 100% curriculum specification match and verified interactive question banks.
0%read

Part 1 of 5Why Transition Metals Catalyse

2.5.7 Transition Metal Catalysts
Why Transition Metals Catalyse
Variable oxidation states
  • A metal can gain and lose electrons easily, so it can form temporary intermediates during a reaction.
Vacant orbitals
  • Partly filled d orbitals can form weak bonds to reactant molecules at a surface.
Lower activation energy
  • The catalyst offers an alternative pathway with a lower activation energy, so more molecules react at a given temperature.
Not consumed
  • The catalyst is regenerated at the end, though it may be poisoned over time.

Part 2 of 5Heterogeneous Catalysis

Definition
  • The catalyst is in a different phase from the reactants, usually a solid catalyst with gaseous reactants.
Contact process
  • Vanadium(V) oxide catalyses SO₂ + ½O₂ → SO₃.
Haber process
  • Iron catalyses N₂ + 3H₂ ⇌ 2NH₃.
Hydrogenation
  • Nickel catalyses the addition of hydrogen to alkenes to make alkanes.
Catalytic converters
  • Platinum, palladium and rhodium convert CO and NOₓ to CO₂ and N₂.
ProcessCatalystReaction
ContactV₂O₅SO₂ + ½O₂ → SO₃
HaberFeN₂ + 3H₂ ⇌ 2NH₃
MargarineNiC=C + H₂ → C–C

Part 3 of 5Mechanism and Poisoning

1
Reactant molecules are adsorbed onto active sites on the catalyst surface.
2
Bonds in the reactants weaken, and the molecules are held in a position where they can react.
3
Product molecules form and are desorbed from the surface, freeing the sites.
4
Impurities such as sulfur in the Haber process and lead in catalytic converters bind to the sites permanently and poison the catalyst.
5
A large surface area, obtained with a finely divided catalyst, increases the number of active sites.

Part 4 of 5Homogeneous Catalysis

Homogeneous Catalysis
Definition
  • The catalyst is in the same phase as the reactants, usually all in aqueous solution.
Peroxodisulfate
  • S₂O₈²⁻ + 2I⁻ → 2SO₄²⁻ + I₂ is slow because two negative ions repel; Fe²⁺ or Fe³⁺ provides a path.
Steps
  • 12Fe²⁺ + S₂O₈²⁻22Fe³⁺ + 2SO₄²⁻ and then 2Fe³⁺ + 2I⁻32Fe²⁺ + I₂
Autocatalysis
  • Mn²⁺ catalyses the reaction between MnO₄⁻ and C₂O₄²⁻, which is why the reaction starts slowly and then speeds up.

Part 5 of 5Exam Checklist & Tips

2.5.7 – Key Points for the Exam

  • Heterogeneous catalyst A catalyst in a different phase from the reactants.
  • Homogeneous catalyst A catalyst in the same phase as the reactants.
  • Adsorption Attachment of molecules to a solid surface.
  • Catalyst poison A substance that binds to catalyst sites and reduces activity.

Common Mistakes

  • Saying a catalyst is used up in the reaction.
  • Stating that the catalyst changes the position of equilibrium.
  • Mixing up homogeneous and heterogeneous definitions.
  • Forgetting to mention adsorption and desorption in heterogeneous catalysis.

Last updated:

\n