← Back to subjects
0
AQA GCSE Chemistry (8462) · 4.6 Rate and extent of chemical change
Mini-Lesson

Rate & Extent of Chemical Change

This mini-lesson walks you through the whole of AQA Topic 4.6: how to measure and calculate rate of reaction, the factors that change it, collision theory, catalysts, the required practical, and reversible reactions with dynamic equilibrium and Le Chatelier's principle.

reactants colliding products formed rate of reaction how fast products appear

Work through each screen, answer the questions as you go (some are wordy, some are calculations) and collect ⭐ stars. Higher-tier-only ideas are clearly flagged. Press Start when you're ready.

Measuring rate

Three ways to measure a rate

The rate of reaction tells you how quickly reactants are used up or products are made. To measure it you follow a quantity that changes over time:

  • Volume of gas given off — collected in a gas syringe (units cm³).
  • Mass lost — a flask on a balance loses mass as gas escapes (units g).
  • Precipitation / turbidity — a solution turns cloudy; time how long until a cross under the beaker disappears.
gas syringe (cm³) balance (g) mass loss cross fades (turbidity)
Choose the method that suits the reaction — a gas-producer suits a syringe; a precipitate suits the disappearing-cross method.
Quick check

Pick the method

?Sodium thiosulfate reacts with hydrochloric acid to form a cloudy yellow precipitate of sulfur. Which method best measures this rate?
Calculating rate

Mean rate of reaction

Over a time interval, the mean rate is simply the quantity made (or used up) divided by the time taken:

mean rate = quantity ÷ timemean rate of reaction = amount of reactant used (or product formed) ÷ time taken

Units depend on what you measured: cm³/s for gas volume, g/s for mass loss, or mol/s for moles.

Worked example

A reaction gives off 48 cm³ of gas in 24 s.

mean rate = 48 ÷ 24 = 2 cm³/s

Calculate

Your turn — mean rate

1A flask loses 6.0 g of mass as carbon dioxide escapes over 120 s. Calculate the mean rate of reaction.
g/s
Hint: mean rate = 6.0 ÷ 120.
Reading rate graphs · Higher for tangent

Reading a rate graph

Plot the quantity (e.g. gas volume) against time and the curve tells the story. The reaction is fastest at the start (steepest gradient), then slows as reactants are used up, and levels off (flat) when the reaction is finished.

volume of gas (cm³) time (s) tangent → gradient = rate here fast (steep) finished (flat)
The steeper the line, the faster the rate. Higher tier: find the rate at one instant by drawing a tangent to the curve and calculating its gradient (change in y ÷ change in x).

Watch out: a steeper curve means a faster rate — not a "bigger" reaction. Two curves can level off at the same height (same amount of product) but one gets there faster.

Higher · Calculate

Rate from a tangent

2Higher tier. A tangent drawn to a volume–time curve rises by 30 cm³ over a horizontal interval of 15 s. Calculate the rate of reaction at that instant.
cm³/s
Hint: gradient = change in y ÷ change in x = 30 ÷ 15.
Collision theory

Why reactions happen

Collision theory says a reaction only happens when particles collide with each other and with enough energy. That minimum energy needed for a collision to be successful is the activation energy (Ea).

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

energy progress of reaction Eₐ (uncatalysed) lower Eₐ (catalyst) reactants products
The "hill" is the activation energy. A catalyst (green dashed) gives an alternative pathway with a lower activation energy, so more collisions succeed.
Quick check

What is activation energy?

?According to collision theory, what does "activation energy" mean?
Factors that affect rate

Five ways to speed it up

AQA expects you to explain each factor using collision theory — what it does to the frequency and/or energy of collisions:

  • Concentration (of solutions) — more particles in the same volume → more frequent collisions.
  • Pressure (of gases) — squeezes particles closer → more frequent collisions.
  • Surface area (of solids) — smaller pieces (e.g. powder) expose more surface → more frequent collisions.
  • Temperature — particles move faster, so collisions are more frequent and have more energy.
  • A catalyst — provides a lower-activation-energy pathway, so more collisions succeed.
one lump powder = more surface area
Same mass, far more exposed surface — so the powder reacts faster.

Watch out: raising the temperature increases both the frequency and the energy of collisions — many students only mention one. The energy effect is the bigger reason temperature speeds reactions up so much.

Sort it

Does it increase the rate?

Tap whether each change would increase or not increase the rate of a reaction.

Catalysts

Catalysts & enzymes

A catalyst speeds up a reaction by providing a different pathway with a lower activation energy — but it is not used up in the reaction, so it does not appear in the chemical equation.

  • Different reactions need different catalysts.
  • Enzymes are biological catalysts — they catalyse the reactions in living things.
  • A catalyst lets you use a lower temperature (saving energy and money) to get the same rate.

Watch out: a catalyst lowers the activation energy and is not used up — it does not "give the particles more energy" and it is not a reactant.

Quick check

How a catalyst works

?Which statement correctly describes a catalyst?
Required practical

Investigating rate

The AQA required practical investigates how a factor changes the rate of reaction. You can vary either:

  • Concentration — e.g. sodium thiosulfate + hydrochloric acid: change the acid concentration and time the disappearing cross (turbidity).
  • Surface area — e.g. marble chips + hydrochloric acid: compare large chips with powder, measuring gas volume or mass loss.

Keep all other variables the same (control variables) so the change you see is caused only by the factor you are testing. A faster rate = shorter time (or steeper graph).

Exam tip: control variables here include temperature, total volume, and the amount of solid — only the tested factor should change.

Quick check

Fair test

?In the marble-chip + acid practical you compare large chips with powder. To make it a fair test, which must you keep the same?
Reversible reactions

Reactions that go both ways

In a reversible reaction the products can react to re-form the reactants. We show this with the symbol:

A + B ⇌ C + Dthe forward reaction (→) and the backward reaction (←) both happen

If a reversible reaction is exothermic in one direction, it is endothermic in the other, by the same amount of energy.

Classic example

Hydrated copper sulfate (blue) ⇌ anhydrous copper sulfate (white) + water.

Heating drives off water (endothermic); adding water back turns it blue again (exothermic).

Quick check

Energy both ways

?Heating blue hydrated copper sulfate to white anhydrous copper sulfate is endothermic. What is the reverse change (adding water back)?
Dynamic equilibrium

Equilibrium in a closed system

In a closed system (nothing in or out), a reversible reaction reaches dynamic equilibrium: the forward and backward reactions happen at exactly the same rate. The amounts of reactants and products then stay constant.

reactants products forward rate backward rate equal rates → amounts constant
"Dynamic" means both reactions are still happening — they just cancel out, so nothing appears to change.

Watch out: at equilibrium the reaction has not stopped — the forward and backward reactions continue at equal rates. It is dynamic, not static.

Quick check

What is happening at equilibrium?

?A reversible reaction in a closed system has reached dynamic equilibrium. Which statement is true?
Higher · Le Chatelier's principle

Shifting the equilibrium

Higher tier only. Le Chatelier's principle: if you change the conditions of a system at equilibrium, the position of equilibrium shifts to oppose that change.

  • Concentration — increase a reactant: equilibrium shifts right (towards products) to use it up.
  • Temperature — increase it: equilibrium shifts in the endothermic direction (to absorb the added energy).
  • Pressure (gases) — increase it: equilibrium shifts to the side with fewer molecules of gas.

Watch out: the system opposes the change you make. Raise the temperature and it favours the endothermic direction; add more of a substance and it shifts away from that substance.

Higher · Predict

Predict the shift

?Higher tier. For N₂ + 3H₂ ⇌ 2NH₃, the forward reaction is exothermic. If the temperature is increased, which way does the equilibrium shift?
Higher · Match

Change & response

Match each change to the way the equilibrium responds. Tap one on the left, then its partner on the right.

Recap

The key ideas to know

Mean rate: quantity ÷ time (cm³/s, g/s, mol/s)

Rate from a curve (HT): gradient of a tangent

Collision theory: collide + enough energy (activation energy)

Factors: concentration, pressure, surface area, temperature, catalyst

Catalyst: lowers Eₐ via a new pathway, not used up; enzymes are biological catalysts

Reversible (⇌): exo one way = endo the other

Dynamic equilibrium: equal forward & backward rates in a closed system

Le Chatelier (HT): the system shifts to oppose the change

You've covered the whole of AQA 4.6 — rate of reaction, collision theory, factors, catalysts, the required practical, reversible reactions and equilibrium. Press Finish to see your score.

🏆

Mini-lesson complete!

⭐⭐⭐

You've worked through Rate & Extent of Chemical Change for AQA GCSE Chemistry. 🎉

Your stars: 0 / 0

Next: test yourself in the Evaluate stage Confidence Quiz, then lock it in with Verify.

📣 Smashed it? Share your score

Challenge a mate to beat your stars, or show a parent how you got on.

→ Back to all subjects