6. Chemical reactions

Syllabus
0620–2026–2027
Section
6
Level
—

6.1 Physical and chemical changes

Syllabus
0620–2026–2027
Topic
6.1
Level
—

Distinguish physical and chemical changes

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.

6.2 Rate of reaction

Syllabus
0620–2026–2027
Topic
6.2
Level
—

Describe how conditions change reaction rate

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.

State what a catalyst does

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.

Measure the rate of a gas-forming reaction

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.

Interpret reaction-rate data and graphs

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.

Describe collision theory

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.

Explain rate changes using collision theory

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.

Link catalysts to activation energy

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.

Evaluate methods for measuring reaction rate

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.

6.3 Reversible reactions and equilibrium

Syllabus
0620–2026–2027
Topic
6.3
Level
—

Recognise a reversible reaction

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.

Reverse hydration by heating or adding water

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.

Define dynamic equilibrium

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.

Predict shifts in equilibrium

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.

Write the Haber process equation

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.

State the Haber process feedstock sources

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.

Recall the typical Haber process conditions

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.

Write the Contact process equilibrium equation

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.

State the Contact process reactant sources

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.

Recall the typical Contact process conditions

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.

Explain industrial equilibrium compromises

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.

6.4 Redox

Syllabus
0620–2026–2027
Topic
6.4
Level
—

Use Roman numerals for oxidation numbers

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.

Define a redox reaction

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.

Define oxidation and reduction by oxygen transfer

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.

Identify redox by oxygen gain and loss

  1. Compare oxygen in each reactant and product. 2. Identify a species that gains oxygen. 3. Identify another species that loses oxygen. 4. If both occur in the same reaction, classify it as redox.

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.

Identify which species is oxidised or reduced

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.

Define oxidation by electrons and oxidation number

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.

Define reduction by electrons and oxidation number

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.

Identify redox by electron transfer

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.

Use oxidation numbers to identify redox

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.

Recognise redox from manganate(VII) and iodide colours

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.

Define an oxidising agent

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.

Define a reducing agent

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.

Identify oxidising and reducing agents

  1. Assign oxidation numbers or write half-equations. 2. Find the species reduced: it is the oxidising agent. 3. Find the species oxidised: it is the reducing agent. 4. Check that electrons lost equal electrons gained.
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.