6. Chemical reactions
- Syllabus
- 0620–2026–2027
- Section
- 6
- Level
- —

| Question to ask | Physical change | Chemical change |
|---|---|---|
| Are new substances formed? | no | yes |
| What happens to the particles? | the same particles change arrangement, spacing or state | atoms are rearranged into different particles as bonds break and form |
| Typical examples | melting, freezing, boiling, condensing, dissolving | combustion, rusting, neutralisation, thermal decomposition |
| Can it be reversed? | often by a physical process | often difficult and may require another chemical reaction |
Classify a change by comparing the substances before and after it. If their chemical identities are unchanged, the change is physical. If one or more new substances with different compositions and properties form, the change is chemical.
Ice melting is physical: H₂O remains H₂O and only its state changes. Magnesium burning is chemical: magnesium and oxygen form a new substance, magnesium oxide. Sulfur melting is physical, but sulfur then burning to form sulfur dioxide is chemical.
A colour change, temperature change, gas, precipitate, or light may suggest a chemical change, but the defining test is formation of new substances. Reversibility is also not a perfect definition: some physical changes are difficult to reverse and some chemical changes can be reversed by another reaction.
| Change | Effect on rate | Reverse change |
|---|---|---|
| increase solution concentration | faster | dilution makes it slower |
| increase gas pressure | faster | lower pressure makes it slower |
| increase solid surface area by using smaller pieces or powder | faster | larger lumps react more slowly |
| increase temperature | faster | cooling makes it slower |
| add a catalyst, including an enzyme | faster | removing it makes the uncatalysed reaction slower |
Reaction rate describes how quickly a reactant is used up or a product is formed. A faster reaction has a greater change in measured quantity per unit time.
When the amount of limiting reactant is unchanged, a faster gas-forming reaction gives a steeper curve and reaches the same final gas volume sooner.
A factor that changes rate does not automatically change the final amount of product. Rate is about how quickly the reaction proceeds; yield depends on the reacting amounts and equilibrium where relevant.
A catalyst increases the rate of a reaction and is chemically unchanged at the end. An enzyme is a biological catalyst.
A catalyst participates in steps of the reaction but is regenerated, so it is not used up overall. It can therefore be recovered with the same chemical identity after the reaction.
| Catalyst changes | Catalyst does not change |
|---|---|
| how quickly products form | the chemical equation |
| time taken to reach completion | the final amount from fixed reactant amounts |
| activation energy | the enthalpy change, ΔH |
A catalyst is not a reactant and does not supply extra product. 'Unchanged' means chemically unchanged at the end, not absent from the reaction pathway.
| Method | Apparatus and measurement | Suitable situation |
|---|---|---|
| gas volume | sealed flask connected to a gas syringe; record volume at regular times | a gas forms and can be collected |
| mass loss | open flask on a balance; record total mass at regular times | a gas forms and escapes |
Measure the reactants, assemble the apparatus, add the final reactant and start the timer together, then record gas volume or mass at fixed time intervals until the reading becomes constant. Calculate a rate from change in volume or mass divided by time.
When testing one factor, change only that independent variable. Keep reactant amounts, concentration where not tested, temperature, solid particle size, apparatus, and timing procedure constant.
A bung is essential for gas collection but not for mass-loss measurement, where the gas must escape. Check connections for leaks before starting a gas-syringe experiment.
On a graph of product formed or reactant used against time, the gradient represents rate. A steeper gradient means a faster rate; a horizontal line means the measured quantity is no longer changing and the reaction has finished.
| Feature | Interpretation |
|---|---|
| steepest section | greatest rate |
| curve becomes less steep | rate is decreasing |
| plateau reached earlier | reaction finishes sooner |
| same plateau height | same final measured amount |
| different plateau height | different final measured amount |
Average rate over an interval = change in measured quantity ÷ time interval. Use the graph scale and include units, such as cm³/s for gas volume or g/s for mass change.
Do not use curve height alone to compare rates. Compare gradients at the same time or over the stated interval; height shows accumulated quantity, not instantaneous speed.
A reaction occurs only when reacting particles collide successfully. A successful collision has enough energy to meet or exceed the activation energy, Ea, and a suitable collision arrangement.
| Particle idea | Link to rate |
|---|---|
| particles per unit volume | affects how close particles are |
| collision frequency | more collisions per second create more opportunities to react |
| kinetic energy | faster-moving particles collide more often and with more energy |
| activation energy, Ea | minimum collision energy needed for reaction |
Use this reasoning chain: condition changes particle behaviour → successful collisions per unit time change → reaction rate changes.
Not every collision causes reaction. Increasing concentration raises collision frequency but does not give each particle more kinetic energy or alter Ea.
| Change | Particle-level cause | Why rate increases |
|---|---|---|
| higher concentration | more particles per unit volume | more collisions per second |
| higher gas pressure | particles are closer; more per unit volume | more collisions per second |
| greater solid surface area | more reactant particles are exposed | more collisions occur at the surface per second |
| higher temperature | particles have more kinetic energy and move faster | collisions are more frequent and a larger fraction meet or exceed Ea |
| add catalyst or enzyme | a lower-Ea pathway is available | a larger fraction of collisions are successful |
For temperature answers, include both effects: particles collide more often and more collisions have sufficient energy. Temperature does not lower the activation energy.
As reactants are used up, their concentration falls, so collision frequency and rate fall. The rate becomes zero when a limiting reactant is completely used up.
Pressure affects gaseous reactants; surface area affects exposed solid. Do not explain either by saying the particles gain energy unless temperature also changes.
A catalyst increases reaction rate by providing an alternative reaction pathway with a lower activation energy, Ea.
At the same temperature, particle kinetic energies are unchanged, but the lower Ea means a larger fraction of collisions have sufficient energy to react. There are therefore more successful collisions per unit time.
| Pathway feature | Without catalyst | With catalyst |
|---|---|---|
| reactant energy | same | same |
| peak height above reactants | higher Ea | lower Ea |
| product energy | same | same |
| ΔH | same | same |
A catalyst does not increase particle energy and does not change ΔH. Only the energy barrier and therefore the rate change.
| Method | Strength | Limitation and improvement |
|---|---|---|
| gas syringe | directly measures gas volume and gives many readings | leaks or a sticking plunger lose accuracy; test seals and use a freely moving, suitable-range syringe |
| mass loss on a balance | simple and records continuous change without collecting gas | only works when gas escapes; small changes, drafts and splashes affect readings; use a suitable-precision balance and a cotton-wool plug |
Choose a method by linking it to the reaction and data needed. Consider whether gas forms, whether it is safe to release, the expected volume or mass change, reading frequency, measurement resolution, and the main systematic losses.
For a fair comparison, control all variables except the one tested. Repeat each condition, identify anomalous results, calculate a mean, and collect readings frequently enough to define the steep initial part of the curve.
An evaluation must connect a specific limitation to its effect on the result and a practical improvement. Merely naming apparatus or saying a method is 'more accurate' is not enough.
In a reversible reaction, products can react to form the original reactants. The forward and reverse reactions are represented together by the symbol ⇌.
For A + B ⇌ C + D, the forward reaction forms C and D from A and B, while the reverse reaction forms A and B from C and D.
Changing conditions can favour one direction, so the mixture may contain different proportions of reactants and products without changing the balanced equation.
The double arrow does not mean the reaction repeatedly switches on and off. Both directions can occur, and their relative rates depend on conditions.
Heating a hydrated salt removes water and forms the anhydrous salt. Adding water to the anhydrous salt reverses the change and reforms the hydrated salt.
| Compound | Hydrated form | After heating | Reverse change |
|---|---|---|---|
| copper(II) sulfate | blue | white anhydrous copper(II) sulfate | add water: white → blue |
| cobalt(II) chloride | pink | blue anhydrous cobalt(II) chloride | add water: blue → pink |
Use the condition to choose direction: heat drives dehydration; water drives hydration. The observed colour identifies which form is present.
Do not swap the colour pairs: hydrated copper(II) sulfate is blue, while hydrated cobalt(II) chloride is pink.
A reversible reaction is at equilibrium in a closed system when the forward and reverse reactions occur at equal rates and the concentrations of reactants and products are no longer changing.
| Microscopic view | Macroscopic view |
|---|---|
| both forward and reverse reactions continue | concentrations remain constant |
| their rates are equal | observable properties no longer change |
A closed system prevents substances entering or leaving, allowing the opposing reactions to establish and maintain equilibrium.
Equal rates do not mean equal concentrations, and equilibrium does not mean both reactions have stopped.
When a condition changes, the equilibrium position shifts in the direction that opposes that change, using the equation and energy information provided.
| Change | Direction favoured |
|---|---|
| increase temperature | endothermic direction |
| decrease temperature | exothermic direction |
| increase gas pressure | side with fewer moles of gas |
| decrease gas pressure | side with more moles of gas |
| add a reactant or product | direction that uses the added substance |
| remove a reactant or product | direction that replaces the removed substance |
| add a catalyst | no change in equilibrium position |
For pressure, count gaseous coefficients only. For temperature, label the forward direction exothermic or endothermic. For concentration, identify which side consumes the changed species. Then state the shift and the resulting yield change.
A catalyst speeds up forward and reverse reactions equally, so equilibrium is reached sooner but its position and equilibrium composition do not change.
N₂(g) + 3H₂(g) ⇌ 2NH₃(g)
One mole of nitrogen reacts reversibly with three moles of hydrogen to form two moles of ammonia. All three substances are gases under the reaction conditions.
The equation is balanced: two nitrogen atoms and six hydrogen atoms appear on each side. The reversible arrow is essential because ammonia can decompose back to nitrogen and hydrogen.
Do not use an ordinary one-way arrow or write NH₄. The Haber product is ammonia, NH₃.
| Feed gas | Main source |
|---|---|
| nitrogen, N₂ | air |
| hydrogen, H₂ | methane, usually from natural gas |
Nitrogen is separated from air. Hydrogen is produced industrially from methane, commonly by reaction with steam before purification.
The purified gases are supplied in the stoichiometric ratio shown by the equation: one volume of nitrogen to three volumes of hydrogen.
Air is the source of nitrogen, not hydrogen. Methane is the named syllabus source of hydrogen.
| Variable | Typical Haber condition |
|---|---|
| temperature | 450 °C |
| pressure | 20 000 kPa, equivalent to 200 atm |
| catalyst | iron |
Keep the values attached to the correct process: Haber uses a very high pressure of 200 atm and an iron catalyst.
Iron increases the rate by lowering activation energy; it does not change the equilibrium yield.
Do not substitute vanadium(V) oxide: that is the catalyst for the Contact process.
2SO₂(g) + O₂(g) ⇌ 2SO₃(g)
Two moles of sulfur dioxide react reversibly with one mole of oxygen to form two moles of sulfur trioxide. Each substance is gaseous under the reaction conditions.
The equation balances two sulfur atoms and six oxygen atoms on each side, and gas moles decrease from three to two in the forward direction.
This is the catalysed equilibrium step. Directly adding water to sulfur trioxide is not this equation and is not the industrial absorption route.
| Reactant | Source |
|---|---|
| sulfur dioxide, SO₂ | burn sulfur in air, or roast sulfide ores in air |
| oxygen, O₂ | air |
Burning sulfur gives S + O₂ → SO₂. Roasting a metal sulfide ore in air also produces sulfur dioxide as the sulfur is oxidised.
The sulfur dioxide is purified before it enters the catalytic converter with oxygen from air.
The syllabus asks for sources of sulfur dioxide and oxygen, not merely a source of elemental sulfur.
| Variable | Typical Contact condition |
|---|---|
| temperature | 450 °C |
| pressure | 200 kPa, equivalent to 2 atm |
| catalyst | vanadium(V) oxide, V₂O₅ |
Contact and Haber both use 450 °C, but Contact uses only 2 atm and the catalyst V₂O₅.
Vanadium(V) oxide increases the rates of both directions and helps equilibrium to be reached faster without changing its position.
Do not use iron or 200 atm; those are Haber process conditions.
| Haber choice | Rate and equilibrium benefit | Safety/economic limit |
|---|---|---|
| 450 °C | fast enough; a lower temperature would favour exothermic ammonia formation | lower temperature is too slow; higher temperature lowers equilibrium yield |
| 200 atm | increases rate and shifts equilibrium to fewer gas moles, increasing NH₃ yield | still higher pressure needs stronger, costlier equipment and increases hazard |
| iron catalyst | increases rate so a moderate temperature can be used | does not increase equilibrium yield |
| Contact choice | Rate and equilibrium benefit | Safety/economic limit |
|---|---|---|
| 450 °C | fast enough; lower temperature would favour exothermic SO₃ formation | lower temperature is too slow; higher temperature lowers yield |
| 2 atm | pressure favours the side with fewer gas moles | much higher pressure gives insufficient extra benefit for its equipment, energy and safety costs |
| V₂O₅ catalyst | increases rate at the compromise temperature | does not change equilibrium yield |
Industrial conditions maximise neither rate nor single-pass equilibrium yield alone. They balance production speed, equilibrium composition, plant cost, energy use, equipment strength, and safety; unreacted gases can be recycled.
A high temperature always speeds both reactions, but for these exothermic forward reactions it lowers the equilibrium product yield. A catalyst improves rate only, not the equilibrium position.
A Roman numeral in a compound name gives the oxidation number of the named element. For example, iron(III) oxide contains iron with oxidation number +3.
| Name | Roman numeral meaning |
|---|---|
| copper(II) oxide | Cu has oxidation number +2 |
| iron(III) chloride | Fe has oxidation number +3 |
| potassium manganate(VII) | Mn has oxidation number +7 |
Determine the oxidation number from the formula and ion charges, then write it in Roman numerals immediately after the element name when required.
The numeral is not the number of atoms or ions in the formula and is written without a plus sign inside the name.
A redox reaction is one in which oxidation and reduction happen simultaneously.
One species is oxidised while another is reduced. The two processes are linked because oxygen or electrons transferred from one species are gained by another.
In Mg + CuO → MgO + Cu, magnesium is oxidised and copper(II) oxide is reduced, so the overall reaction is redox.
A reaction is not redox if only mixing, precipitation, or acid–base neutralisation occurs without simultaneous oxidation and reduction.
| Process | Oxygen change |
|---|---|
| oxidation | gain of oxygen |
| reduction | loss of oxygen |
In CuO + H₂ → Cu + H₂O, hydrogen gains oxygen and is oxidised; copper(II) oxide loses oxygen and is reduced.
Compare each substance before and after the reaction. Track oxygen attached to the substance, not merely whether oxygen gas appears in the equation.
Reduction does not mean a substance becomes physically smaller. In this definition it specifically means loss of oxygen.
For 3Fe + 4H₂O → Fe₃O₄ + 4H₂, iron gains oxygen and is oxidised, while water loses oxygen to form hydrogen and is reduced. Both changes make the reaction redox.
In AgNO₃ + NaCl → AgCl + NaNO₃, no species gains oxygen while another loses it, so oxygen transfer does not identify a redox change.
Finding oxygen in an equation is not enough. There must be simultaneous gain and loss of oxygen between species.
| Observation | Classification |
|---|---|
| species gains oxygen | oxidised |
| species loses oxygen | reduced |
| species loses electrons or oxidation number rises | oxidised |
| species gains electrons or oxidation number falls | reduced |
In Zn + CuO → ZnO + Cu, zinc gains oxygen and is oxidised; copper(II) oxide loses oxygen and is reduced.
A complete identification names the species, states oxidation or reduction, and gives the relevant oxygen, electron, or oxidation-number evidence.
Name the whole species shown in the reaction when oxygen is transferred; do not identify oxygen itself as the substance reduced.
Oxidation is loss of electrons and an increase in oxidation number.
Zn → Zn²⁺ + 2e⁻ shows oxidation: zinc loses two electrons and its oxidation number increases from 0 to +2.
| Evidence | Oxidation sign |
|---|---|
| electrons in products of a half-equation | electrons were lost |
| oxidation number becomes more positive | oxidation number increased |
Oxidation is electron loss, not gain. The species that loses electrons becomes more positive or less negative.
Reduction is gain of electrons and a decrease in oxidation number.
Cu²⁺ + 2e⁻ → Cu shows reduction: copper ions gain two electrons and the oxidation number decreases from +2 to 0.
| Evidence | Reduction sign |
|---|---|
| electrons in reactants of a half-equation | electrons were gained |
| oxidation number becomes less positive or more negative | oxidation number decreased |
Reduction is electron gain, not loss. A decreasing oxidation number moves numerically downward, such as +3 to +2 or 0 to −1.
A reaction is redox when electrons are transferred: one species loses electrons and another species gains the same number of electrons.
For Zn + Cu²⁺ → Zn²⁺ + Cu: Zn → Zn²⁺ + 2e⁻ is oxidation, while Cu²⁺ + 2e⁻ → Cu is reduction. The electrons cancel when the half-equations are combined.
Identify the electron donor and electron acceptor. If no oxidation number changes and no electron transfer occurs, the reaction is not redox.
Electrons travel through an external circuit in a cell, not through the electrolyte as free electrons; ions carry charge in the solution.
| Rule | Result |
|---|---|
| uncombined element | oxidation number 0 |
| monatomic ion | oxidation number equals ion charge |
| neutral compound | oxidation numbers sum to 0 |
| polyatomic ion | oxidation numbers sum to the ion charge |
In SO₄²⁻, oxygen is −2: S + 4(−2) = −2, so sulfur is +6. Show the total equation before solving the unknown oxidation number.
Compare oxidation numbers before and after: an increase identifies oxidation and a decrease identifies reduction. A redox reaction contains both changes.
Subscripts multiply oxidation numbers; they are not oxidation numbers themselves. The oxidation number of O₂, Cl₂, metals, and all other uncombined elements is 0.
| Reagent | Starting colour | Redox observation | What it detects |
|---|---|---|---|
| acidified aqueous potassium manganate(VII) | purple | turns colourless | a reducing agent reduces manganate(VII) |
| aqueous potassium iodide | colourless | turns brown as iodine forms | an oxidising agent oxidises iodide ions |
Use the reagent's own change to identify the unknown: manganate(VII) is reduced, so the tested substance is reducing; iodide is oxidised to iodine, so the tested substance is oxidising.
Iodide loses electrons: 2I⁻ → I₂ + 2e⁻. The brown iodine colour is evidence of this oxidation.
Potassium manganate(VII) must be acidified for the stated purple-to-colourless test. Do not confuse brown iodine with a brown precipitate.
An oxidising agent oxidises another substance and is itself reduced.
It accepts electrons from the other species, so its own oxidation number decreases.
In Zn + Cu²⁺ → Zn²⁺ + Cu, Cu²⁺ is the oxidising agent: it causes zinc to lose electrons and itself gains electrons to form copper.
The agent is named for what it does to the other substance. The oxidising agent is reduced, not oxidised.
A reducing agent reduces another substance and is itself oxidised.
It donates electrons to the other species, so its own oxidation number increases.
In Zn + Cu²⁺ → Zn²⁺ + Cu, zinc is the reducing agent: it supplies electrons that reduce Cu²⁺ and is itself oxidised to Zn²⁺.
The reducing agent is oxidised. Do not select the species whose oxidation number decreases; that species is the oxidising agent.
| Species change | Role |
|---|---|
| gains electrons / oxidation number decreases / loses oxygen | oxidising agent |
| loses electrons / oxidation number increases / gains oxygen | reducing agent |
For Cl₂ + 2Br⁻ → 2Cl⁻ + Br₂, chlorine gains electrons and is the oxidising agent; bromide ions lose electrons and are the reducing agent.
Do not label an agent from its name alone. Track what happens to that species in the specific reaction.