Library › Chemistry 0620 › Chemical Change & Rate of Reaction
O Level · Chemistry 0620

Chemical Change & Rate of Reaction

Revise Chemical Change & Rate of Reaction for Chemistry 0620 (O Level) — revision notes and instant AI marking.

📖 Revision notes

Chemical Change & Rate of Reaction

Cambridge IGCSE Chemistry

The Big Idea: Reactions happen when particles collide with enough energy. You can speed up or slow down any reaction by changing concentration, temperature, surface area, or adding a catalyst.

Quick Summary

Physical vs Chemical

Physical changes don't create new substances; chemical changes do and are usually hard to reverse.

Five Key Factors

Concentration, temperature, surface area, pressure, and catalysts all affect how fast reactions go.

Collision Theory

Reactions need particle collisions with enough energy (activation energy) to break bonds and form new substances.

Rate Measurement

Track how fast reactants disappear or products form using mass loss, gas volume, or colour change.

Graph Interpretation

Reaction rate is the gradient of a product-vs-time curve. Steeper at the start, then levels off as reactants run out.

Limiting Reactant

The reactant that runs out first determines how much product you can make.

1. Physical & Chemical Changes

What's the difference?

This is one of the first concepts examiners test because students often mix them up. Here's the clearest way to think about it:

Physical Change:

No new substances are created. The matter stays the same chemically, just looks or feels different. Easy to reverse.

Examples: Melting ice into water, dissolving salt in water, tearing paper, mixing oil and water.

Chemical Change:

New substances with different properties are formed. Bonds break and reform. Usually hard or impossible to reverse.

Examples: Burning paper to ash, rusting iron, cooking an egg, acid reacting with magnesium.

How to Tell the Difference (Exam Tip): Ask yourself: "If I did this in reverse, would I get the exact same substance back?" If yes, it's probably physical. If no (you've created something brand new), it's chemical.

Signs of a Chemical Reaction

Examiners love asking you to describe what happens. Watch for these:

🎨 Colour Change

One of the easiest signs. For example, copper is orange-brown. When it reacts with silver nitrate (colourless), you get silver (grey) and copper nitrate (blue). Two clear colour changes = chemical reaction happened.

🌡️ Temperature Change

Exothermic: Releases heat. Combustion, neutralisation, rusting. The container gets hot.

Endothermic: Absorbs heat. Photosynthesis, dissolving ammonium chloride. The container gets cold (sometimes used in cold packs).

💨 Effervescence (Fizzing)

Gas is produced. Usually hydrogen gas when a metal reacts with acid, or carbon dioxide when an acid reacts with a carbonate.

Other signs:

Light being produced (like burning magnesium burning super bright), smell changing, pH changing.

Practice Question 1
You mix copper powder with dilute hydrochloric acid in a test tube. The mixture fizzes vigorously and the test tube becomes hot. Is this a physical or chemical change? Explain your reasoning with two pieces of evidence.

2. Rates of Reaction — What Makes Reactions Go Faster?

This is a big exam topic. You need to know four factors that affect rate, and more importantly, why they affect rate using collision theory.

Rate of Reaction =

How much product is made (or reactant used up) per unit time. Usually measured in cm³/s or g/s.

Factor 1: Concentration (or Pressure for Gases)

Higher concentration = faster reaction.

Why? If there are more particles in the same volume, they bump into each other more often. More collisions = more successful collisions per second = faster reaction.

On a graph: The curve for high concentration is steeper at the start (faster initial rate) and levels off sooner (finishes quicker). Both lines reach the same height eventually (same amount of product) because you're using the same amount of reactant—just changing how fast it reacts.

┌──────────────────────────────────────┐ │ MASS/VOLUME OF PRODUCT │ ├──────────────────────────────────────┤ │ ╱╱ High concentration │ ╱╱ │ ╱╱ │ ╱ Low concentration │ ╱ │ ╱ └──────────────────────────────────────┘ TIME (Note: Both reach same final amount)
Exam Trick: Students often think high concentration produces MORE product. Wrong. It makes the SAME product FASTER. The limiting reactant determines the total amount.

Factor 2: Temperature

Higher temperature = much faster reaction.

Why? Warmer particles move faster, so they collide more frequently AND with more energy. More collisions with enough energy to break bonds = more successful collisions.

Rule of thumb: For every 10°C increase, the rate roughly doubles. That's huge. A small temperature change has a big effect.

On a graph: Same pattern as concentration—steeper at the start for the higher temperature line.

Factor 3: Surface Area

Powdered reactant reacts faster than lumps. Larger surface area = faster reaction.

Why? If a solid is powdered, more of its surface is exposed. More surface available for the other reactant to hit = more frequent collisions.

Quick maths: A 2 cm cube has surface area 24 cm². Cut it into 8 smaller cubes, and the total surface area is now 48 cm²—doubled! Same amount of solid, twice the surface exposed.

Real-world example: Why does a firework explode (fast) but a lump of coal burns slowly? The firework powder has huge surface area. Coal is a lump. Same chemical reaction, massively different rates.

Factor 4: Catalysts

A catalyst speeds up a reaction without being used up or changed. It's the same at the end as the start.

How it works: A catalyst lowers the activation energy. Think of it like providing an easier route for the reaction. More particles have enough energy to react.

Key point: A catalyst does NOT change how much product is made—just how fast it's made. And you use very little catalyst; a tiny amount does a huge job.

On a graph: The curve with a catalyst is steeper at the start and levels off sooner, but both reach the same final amount of product.

Industrial example: Iron is used as a catalyst in the Haber Process to make ammonia. Without it, the reaction would be uselessly slow. With it, industry can produce huge amounts quickly.
Practice Question 2
A student reacts marble chips (calcium carbonate) with dilute hydrochloric acid. They measure the volume of CO₂ gas produced over time. They repeat the experiment with the same marble chips crushed into powder, keeping everything else the same. Sketch or describe what the graph would look like. Would the total volume of gas be the same or different?

3. Collision Theory — Why Things React (Extended Tier)

This is the theory that explains all four factors above. It's the "why" behind the "what."

Collision Theory States:

For a reaction to happen: (1) Particles must collide with each other. (2) The collision must have enough energy to break bonds. (3) The minimum energy needed is called the activation energy.

Successful vs Unsuccessful Collisions

Successful Collision

Particles hit head-on with enough energy (≥ activation energy). Bonds break, atoms rearrange, and new products form.

Unsuccessful Collision

Particles either don't hit hard enough, or they bounce at the wrong angle. No reaction happens; they just bounce apart unchanged.

The fact: Most collisions are unsuccessful. Only a tiny fraction have enough energy. That's why temperature is so powerful—a small increase in heat means WAY more collisions have enough energy.

Why Each Factor Affects Rate (The Deep Explanation)

Concentration → More particles per unit volume → More collisions per second

If you double the concentration, you double the number of particles. Double the collisions. Double the successful collisions. Rate doubles.

Temperature → Particles move faster → More collisions AND higher energy per collision

This is the big one. Higher KE means two things: (1) Faster particles = more frequent collisions. (2) Higher energy per collision = more surpass the activation energy threshold. Both effects combined = huge rate increase.

Surface Area → More solid surface exposed → More contact points between reactants

A larger surface area means more area available for reactant particles to collide with the solid. More collision sites = more collisions per second.

Catalyst → Lowers activation energy → Higher proportion of collisions have enough energy

A catalyst doesn't change the energy of colliding particles. Instead, it provides an alternative reaction pathway that requires less energy. Suddenly, many more collisions are successful, even without heating.

Key Insight: Temperature is special because it's the ONLY factor that directly increases the energy of the collisions themselves. Concentration, surface area, and catalysts only affect the NUMBER of (attempted) collisions or the threshold needed.
ACTIVATION ENERGY DIAGRAM (With and Without Catalyst) ENERGY │ ╱╲ Uncatalysed path │ ╱ ╲_ │Ea (uncatalysed) │ ╱ │ ╱ ╱╲ Catalysed path │ ╱ ╱ ╲_ │ ╱Ea (catalysed) │──┴──────────────────── Reactants → Products The catalysed path has a LOWER activation energy (Ea). More particles have enough energy to react. Result: Faster reaction at the same temperature.

4. Investigating the Rate of a Reaction

Examiners often describe an experiment and ask you to explain what's happening or predict results. Know these three classic setups.

Method 1: Measuring the Volume of Gas Produced

Classic Experiment: Sodium thiosulfate + dilute hydrochloric acid → sulfur precipitate (yellow solid) + other products

Setup:

  • Measure 50 cm³ of sodium thiosulfate solution
  • Mix with 5 cm³ of dilute HCl in a flask
  • The solution becomes cloudy (yellow sulfur forms)
  • Start a stopwatch and look down from above
  • Stop when you can no longer see a cross drawn on paper under the flask
  • Record the time. The faster the cloudiness appears, the faster the rate.

Why this works: The rate of sulfur formation = the rate of reaction. Slower reaction = longer time to become opaque. Faster reaction = shorter time.

Exam Point: This method is simple but has a human error issue: different people see "invisible" at different levels of cloudiness. That's a weakness to mention if asked to evaluate the method.

Method 2: Measuring Gas Volume (Gas Syringe or Inverted Measuring Cylinder)

Classic Experiment: Magnesium + dilute HCl → magnesium chloride + hydrogen gas

Setup: Use a gas syringe or upside-down measuring cylinder filled with water to collect the hydrogen gas produced.

Why this works: You measure gas volume at regular time intervals and plot a graph. Volume increases as the reaction proceeds. The steeper the curve, the faster the reaction.

To change variables: Use different concentrations of acid (concentration factor), different sizes of magnesium pieces (surface area factor), different temperatures (temperature factor).

Method 3: Measuring Mass Loss

Setup: Place a flask with a reaction on a balance. Gas escapes through cotton wool (which lets gas out but prevents solids from splattering). Measure the mass at regular intervals.

Why this works: As gas escapes, the flask gets lighter. The rate of mass loss tells you the reaction rate.

Limitation: This doesn't work for gases with very low molecular mass (like H₂), because the mass change is too small to measure accurately on a typical balance.

Real Experiment: Testing the Effect of Concentration

Experiment design: Same as the sodium thiosulfate method above, but use different concentrations of sodium thiosulfate (e.g., dilute different amounts with water).

Results: Higher concentration → faster reaction → cross disappears sooner.

Why? More solute particles per unit volume → more frequent collisions → more successful collisions.

Practice Question 3
A student uses the magnesium + HCl experiment with a gas syringe. They repeat at 30°C, 40°C, and 50°C, measuring the volume of hydrogen gas produced over time. (a) Sketch what the three curves would look like on one graph. (b) Would the final volume of gas be the same for all three runs?

5. Interpreting Data and Rate Calculations

What Graphs Tell You

Shape of the Curve (Product vs Time)

At the start: Steep gradient = fast reaction (lots of reactant, lots of successful collisions).

In the middle: Gradient becomes less steep = reaction slows down (some reactant used up, fewer collisions).

At the end: Horizontal line (gradient = 0) = reaction stopped (one reactant ran out, no more collisions possible).

Comparing Two Reactions

Curve 1 is steeper at the start than Curve 2? Curve 1 is faster (higher initial rate).

Curve 1 reaches horizontal sooner? Curve 1 finishes faster.

Curve 1 is higher at the end? Curve 1 made more product (maybe a different amount of reactant, or a limiting reactant difference).

Calculating Rate at a Specific Time

To find the rate at a specific point, you draw a tangent to the curve (a straight line that just touches the curve at that point).

Rate = Gradient of Tangent = (Change in y) / (Change in x)

Example: A graph shows volume of CO₂ (y-axis) vs time in seconds (x-axis). At 20 seconds, the tangent line goes from (10 seconds, 5 cm³) to (30 seconds, 29 cm³).

Rate = (29 − 5) / (30 − 10) = 24 / 20 = 1.2 cm³/s

Exam tip: When drawing tangents, use a ruler and draw a long line. Small tangent lines = large errors. And always show your working when calculating.

Limiting Reactants and Product Amount

The limiting reactant is the one that runs out first and determines how much product you can make.

On a graph: If you double the concentration of Reactant A but keep Reactant B the same, you might get twice as much product (if B becomes the new limiting reactant). Or you might get the same product (if A was always in excess). The shape of the curve and how high it reaches tells you what's limiting.

Key: Changing the amount of the EXCESS reactant doesn't change total product. Changing the amount of the LIMITING reactant does change product. The rate is affected by concentration, but the total product is determined by the limiting reactant.
Practice Question 4
Look at a graph of two reactions: Reaction A (with catalyst) and Reaction B (without catalyst), both measuring gas volume over time. Both curves level off at exactly 50 cm³. The curve with catalyst is much steeper at the start and reaches 50 cm³ in 30 seconds. Without catalyst, it takes 90 seconds. Explain the similarities and differences between these curves using collision theory.

What to Memorise

Physical Change
No new substances formed, usually reversible (melting, dissolving, mixing).
Chemical Change
New substances with different properties formed, usually hard to reverse (burning, rusting, reactions).
Rate of Reaction
How much product forms (or reactant is used) per unit time. Measured in cm³/s, g/s, etc.
Concentration Effect
Higher concentration → more particles per unit volume → more frequent collisions → faster rate.
Temperature Effect
Higher temperature → faster particle movement → more frequent collisions + higher energy per collision → much faster rate. (~2× every 10°C)
Surface Area Effect
Larger surface area → more contact between reactants → more frequent collisions → faster rate.
Catalyst
Speeds up reaction without being used up. Lowers activation energy. Doesn't change total product amount.
Activation Energy
Minimum energy colliding particles must have to react. Only collisions with Ea ≥ activation energy are successful.
Successful Collision
Particles collide with ≥ activation energy and correct orientation. Bonds break, new products form.
Limiting Reactant
The reactant that runs out first. Determines total amount of product made.
Exothermic Reaction
Releases heat/thermal energy. Temperature of surroundings increases.
Endothermic Reaction
Absorbs heat/thermal energy. Temperature of surroundings decreases.

Concepts Checklist

Tick off each concept as you master it. Use this to focus your revision.

Exam Tips — Common Mistakes & What Examiners Look For

Mistake 1: Confusing "rate" with "amount of product"

Rate is how FAST the reaction goes. Amount is how MUCH product is made. A catalyst makes reactions faster but doesn't make more product. Concentration makes reactions faster but doesn't make more product (total is determined by the limiting reactant).

Mistake 2: Not explaining WHY something affects rate

Just saying "higher concentration = faster rate" gets you a fact. Examiners want the mechanism: "Higher concentration means more particles per unit volume, so collisions happen more frequently, so more successful collisions per second, so faster rate." Use collision theory.

Mistake 3: Saying a catalyst is "used up" or "consumed"

Wrong. A catalyst is not used up. Same mass at the end as the start. It provides an alternative pathway but isn't part of the final products.

Mistake 4: Getting graphs wrong

When two curves are compared: (1) Steeper initial gradient = faster rate. (2) Reaching horizontal sooner = reaction finished faster. (3) Different final heights = different total product (different amounts of limiting reactant or different reactants).

Mistake 5: Forgetting activation energy in your explanation

When explaining temperature, don't just say "particles move faster." Say: "Particles have more kinetic energy. This increases both collision frequency AND the proportion of collisions with energy ≥ activation energy."

What Examiners ALWAYS ask:

• Explain how [factor] affects rate using collision theory.
• Compare two graphs and explain the differences.
• Design an experiment to test [variable].
• Draw a tangent and calculate rate.
• Describe what you would observe in this reaction (colour, temperature, gas, etc.).

General Exam Strategy:

Always link back to collision theory. More collisions? Explain why. More successful collisions? Explain which part of the mechanism changed (number, frequency, energy, activation energy). Don't just state facts—explain mechanisms.

Chemical Change & Rate of Reaction — IGCSE Chemistry Revision Guide

Study offline. Click "Show Answer" buttons to reveal answers. Tick the checklist as you master each concept.

What's inside
📖 Revision notes 🎯 Learn mode ✦ AI flashcards ✓ Instant AI marking 🧊 3D explorers 🧪 Experiments & simulations 📈 Progress tracking
📄 Practise Chemical Change & Rate of Reaction with Chemistry 0620 past papers Every paper with its mark scheme — answer online, marked instantly. Open →

Practise Chemical Change & Rate of Reaction free

You have just read the whole note. Create a free account for the flashcards and practice questions on this topic, marked instantly against the official answer. No credit card.

Practise this topic free →

More Chemistry topics