Catalysts in Action (College Board AP® Chemistry): Revision Note

Oluwapelumi Kolawole

Written by: Oluwapelumi Kolawole

Reviewed by: Stewart Hird

Updated on

Catalysts & Binding

  • Some catalysts speed up a reaction by binding to the reactant(s)

    • The bound reactants are oriented more favorably or react with a lower activation energy, and the catalyst–reactant complex is a new reaction intermediate

    • Many enzymes work this way

  • Catalysts are sometimes described as:

    • Homogeneous (in the same phase as the reactants)

    • Heterogeneous (in a different phase from the reactants)

  • The AP course groups catalysis by how it works:

    • Binding (for example, enzymes)

    • Acid–base catalysis

    • Surface catalysis

  • Heterogeneous catalysts are in a different phase to the reaction

    • For example, the use of platinum or palladium metals (solid) in organic reactions such as hydrogenation reactions

  • Homogeneous catalysts exist in the same phase as the reactants

    • Homogeneous catalysts most often catalyze gaseous and aqueous reactions

    • For example, aqueous zinc chloride, ZnCl2, is used to catalyze the organic reaction between hydrogen chloride and alcohol

Enzyme catalysis

  • Enzymes are examples of biological catalysts that can speed up the rate of biological reactions in living organisms

    • Most enzymes are large protein molecules with molecular weights ranging from about 10,000 to about 1 million amu

    • Enzymes are very selective in the reactions they catalyze

    • Some are absolutely specific, operating for only one substance in only one reaction

  • Enzyme molecules possess an active site

    • This is part of the molecule with a shape that allows a specific reactant molecule (substrate) to bind

    • The binding between the substrate and active site involves dipole-dipole attractions, hydrogen bonds, and dispersion forces

  • Two models currently exist to explain how an enzyme and its substrate interact

    • Model 1:

      • The substrate molecule fits into the active site on the enzyme molecule, somewhat in the way a key fits into a lock

      • This results in the formation of an enzyme-substrate complex as a reaction intermediate

      • On binding to the enzyme, the substrate may have bonds weakened or new bonds formed that help yield the products

    • Model 2:

      • This is often called the induced fit model

      • This suggests that the active site of an enzyme changes its shape to fit its substrate

Enzyme catalysis models

Two-part diagram of enzyme models: A, lock-and-key, where two substrates fit an active site that is already the right shape to form a complex on the enzyme; B, induced fit, where the active site changes shape to fit the substrates.
Diagram A shows the lock and key model relationship between the enzyme’s active site and the reactant molecules (substrate) while diagram B shows the enzyme’s active site changing shape to allow the substrates to bind.

Catalysts & Covalent Bonding

  • Some heterogeneous catalysts can speed up the reaction rate through the formation of weak covalent bonds with the reactant molecules

  • One example is the decomposition of N2O on gold, the solid catalyst

N2O (g) → N2 (g) + ½ O2 (g)

  • In the catalyzed decomposition, N2O is chemically adsorbed on the surface of the solid gold

    • A weak covalent bond is formed between the oxygen atom of an N2O molecule and a gold atom on the surface

    • This weakens the bond joining nitrogen to oxygen, making it easier for the N2O molecule to break apart

    • The process can be represented as follows:

Decomposition of N2O on a gold catalyst

N≡N–O (g) + Au (s) → N≡N···O···Au (s) → N≡N (g) + O···Au (s)

  • The equation shows the catalytic action of gold in the decomposition of dinitrogen oxide, N2O

  • A weak covalent bond, represented by the dotted lines, is formed between oxygen and the solid gold catalyst

  • The oxygen atoms left on the surface then combine and leave as O2 (g), giving the overall equation:

N2O (g) → N2 (g) + ½O2 (g)

  • Another example of catalysis involving covalent bond formation between a catalyst and the reactants is acid-base catalysis

    • In acid–base catalysis, a reactant or intermediate gains or loses a proton (H+). For example, H3O+ donates a proton to the reactant (protonation), forming a more reactive intermediate

    • A later step gives the proton back, so the acid catalyst is regenerated

    • The hydrolysis of an ester (ester + water → carboxylic acid + alcohol), catalyzed by H3O+ from hydrochloric acid, is a good example

Acid-catalyzed hydrolysis of esters

Mechanism for the acid-catalyzed hydrolysis of ethyl acetate: H3O+ protonates the ester to give a protonated intermediate, which reacts with water to give acetic acid and ethanol.
Mechanism for the acid-catalyzed hydrolysis of an ester. H3O+ protonates the ester, forming a protonated intermediate that reacts with water; H3O+ is regenerated in the final step

Examiner Tips and Tricks

To argue that H3O+ is a catalyst, point to the steps: it is consumed in an early step and regenerated in a later step, so it does not appear in the overall equation. The protonated species is an intermediate (made, then used up).

Do not call H3O+ a spectator ion, and do not justify it only with "catalysts speed up reactions"

Surface Catalysis

  • In industry, many reactions are catalyzed by the surfaces of solids

    • These reactions often involve gaseous reactants being adsorbed on the surface of a solid catalyst

    • Adsorption refers to the collection of one substance on the surface of another substance

Examples of surface catalysis

  • Some of the more important examples of surface catalysis include:

    • The Contact Process - a multistep reaction for making sulfuric acid

2SO2 (g) + O2 (g) →V2O5(s) 2SO3 (g)

  • The Haber Process - for making ammonia

N2 (g) + 3H2 (g) →Fe (s) 2NH3 (g)

  • Catalytic converters - for the removal of toxic / poisonous gases from car exhausts

2CO (g) + 2NO (g) →Pt/Pd/Rh (s) 2CO2 (g) + N2 (g)

  • Hydrogenation - for the hardening of vegetable oils

C2H4 (g) + H2 (g) →Ni/Pt/Pd (s) C2H6 (g)

How surface catalysis works

  • Surface catalysis happens in three main stages:

    • Adsorption: the reactants bind to the surface (physically, by weak forces, or chemically, by covalent bonds), which weakens bonds in the reactants

    • Reaction: the bound intermediates react with each other in new elementary steps on the surface

    • Desorption: the products leave the surface

Examiner Tips and Tricks

The CED states: "In surface catalysis, a reactant or intermediate binds to, or forms a covalent bond with, the surface. This introduces elementary reactions involving these new bound reaction intermediate(s)."

When you explain surface catalysis, name the bound intermediate and describe the new elementary steps on the surface

Surface catalysis in hydrogenation

  • Hydrogenation is an important industrial process that is used to convert unsaturated fats, occurring as oils, to saturated fats

  • Hydrogenation involves the use of a heterogeneous catalyst

  • Hydrogenation adds hydrogen across a C=C double bond, converting it into a C–C single bond

  • A simple example of hydrogenation involves ethylene and hydrogen gas:

C2H4 (g) + H2 (g) → C2H6 (g)

  • Without a catalyst, this reaction is very slow

    • However, when the reaction is catalyzed by a metal such as nickel, palladium or platinum, the rate increases dramatically

    • The role of the catalyst is to allow the formation of metal–hydrogen interactions that weaken the H‒H bond, making the reaction easier

How hydrogenation happens

  • Using the ethylene and hydrogen example, hydrogen and ethylene adsorb onto the catalyst surface, where the reaction occurs

  • This weakens the H–H covalent bond, which eventually breaks

  • This leaves two H atoms loosely bonded to the metal surface but relatively free to move

  • When a hydrogen atom encounters an adsorbed ethylene molecule, it forms a single covalent bond with one of the carbon atoms

    • Effectively, the C=C pi bond is destroyed

  • This leaves an ethyl group, C2H5, bonded to the surface via a metal-to-carbon sigma bond

    • This sigma bond is relatively weak

    • So, when the other carbon atom also encounters a hydrogen atom, a bond is readily formed

    • This forms an ethane molecule, C2H6, which is released from the metal surface

Surface catalytic hydrogenation of ethylene

Four-step diagram on a metal surface: hydrogen and ethylene adsorb; the H–H bond breaks into mobile H atoms; one H adds to C2H4 to give a C2H5 intermediate; a second H adds to give ethane, C2H6, which desorbs.
Diagram showing the reaction mechanism between ethylene and hydrogen on the surface of platinum metal catalyst
  • In general, it is important to note that for solid catalysts, an increase in surface area makes them more effective

Unlock more, it's free!

Join the 100,000+ Students that ❤️ Save My Exams

the (exam) results speak for themselves:

Build on this topic

Oluwapelumi Kolawole

Author: Oluwapelumi Kolawole

Expertise: Chemistry Content Creator

Oluwapelumi is a Pharmacist with over 15000+ hours of AP , IB, IGCSE, GCSE and A-Level chemistry tutoring experience. His love for chemistry education has seen him work with various Edtech platforms and schools across the world. He’s able to bring his communication skills as a healthcare professional in breaking down seemingly complex chemistry concepts into easily understood concepts for students.

Stewart Hird

Reviewer: Stewart Hird

Expertise: Chemistry Content Creator

Stewart has been an enthusiastic GCSE, IGCSE, A Level and IB teacher for more than 30 years in the UK as well as overseas, and has also been an examiner for IB and A Level. As a long-standing Head of Science, Stewart brings a wealth of experience to creating Topic Questions and revision materials for Save My Exams. Stewart specialises in Chemistry, but has also taught Physics and Environmental Systems and Societies.