Core Practicals Overview — Chemistry
This lesson covers the key Chemistry core practicals for Edexcel GCSE Combined Science (1SC0). As with Biology, around 15% of marks assess practical knowledge. You must know the method, variables, results and safety precautions for each practical.
Core Practical 4: Investigating Paper Chromatography
Aim
To use paper chromatography to separate and identify substances in a mixture (e.g. food colourings or inks).
Method
- Draw a pencil line (the origin or baseline) about 2 cm from the bottom of a piece of chromatography paper. Use pencil because it is insoluble and will not dissolve in the solvent.
- Place small spots of the samples and known reference substances on the pencil line, equally spaced.
- Pour a shallow layer of solvent (e.g. water or ethanol) into a beaker — the solvent level must be below the pencil line.
- Place the paper in the beaker and cover with a lid (to prevent evaporation of the solvent).
- Allow the solvent to rise up the paper by capillary action.
- Remove the paper when the solvent front is near the top and immediately mark the solvent front with a pencil line.
- Allow the paper to dry.
- Calculate Rf values for each spot.
Calculating Rf Values
Rf=distance moved by solvent frontdistance moved by substance
- Distances are measured from the pencil baseline to the centre of the spot (substance) or to the solvent front line.
- R_f values are always between 0 and 1 (they have no units).
- Each substance has a characteristic R_f value in a given solvent.
Variables
| Variable type | Variable |
|---|
| Independent variable (IV) | Different substances / samples being tested |
| Dependent variable (DV) | R_f value (distance moved by substance / distance moved by solvent) |
| Control variables | Same solvent, same paper, same temperature, same volume of sample applied |
Key Results and Conclusions
- A pure substance produces one spot.
- A mixture produces multiple spots (one for each component).
- If a spot from an unknown sample has the same Rf value as a known reference, they are likely the same substance.
Exam Tip: If a question asks why we use pencil (not pen) for the baseline, the answer is: pencil is insoluble in the solvent and will not interfere with the results.
Safety
- If using ethanol as the solvent, keep it away from naked flames (flammable).
- Work in a well-ventilated area.
Core Practical 5: Preparing a Pure, Dry Sample of a Soluble Salt
Aim
To prepare a pure, dry sample of a soluble salt (e.g. copper sulfate) by reacting an insoluble base (e.g. copper oxide) with a dilute acid (e.g. sulfuric acid).
Method
- Pour about 25 cm³ of dilute sulfuric acid into a beaker and warm gently on a tripod and gauze.
- Add copper oxide (the insoluble base) a spatula at a time, stirring after each addition.
- Continue adding copper oxide until it is in excess — you will see unreacted black powder at the bottom of the beaker.
- Filter the mixture to remove the excess copper oxide (the filtrate contains the dissolved salt).
- Pour the filtrate into an evaporating basin.
- Heat the solution gently until about half the water has evaporated (you should see crystals starting to form at the edges).
- Leave the solution to cool and crystallise slowly (this gives larger, purer crystals).
- Filter off the crystals, wash with a small amount of cold distilled water and pat dry with filter paper.
Why Add Excess Base?
Adding excess ensures that all the acid has reacted. This is important because:
- The remaining solution should contain only the salt and water (no unreacted acid).
- Excess base is removed by filtration.
Variables
| Feature | Detail |
|---|
| Acid used | Dilute sulfuric acid |
| Base used | Copper oxide (insoluble) |
| Salt produced | Copper sulfate |
| Key technique | Filtration, evaporation, crystallisation |
Key Equation
copper oxide+sulfuric acid→copper sulfate+water
CuO+H2SO4→CuSO4+H2O
Exam Tip: The question might ask you to adapt this method for a different acid-base pair (e.g. zinc oxide + hydrochloric acid → zinc chloride). The method is the same — just change the reagents.
Safety
- Wear eye protection (goggles) throughout.
- Handle hot apparatus with care (use tongs or heatproof mat).
- Dilute acid is an irritant — wash skin immediately if splashed.
Core Practical 6: Investigating Electrolysis
Aim
To investigate the electrolysis of an aqueous solution (e.g. copper sulfate solution) using inert electrodes.
Method
- Fill a beaker with copper sulfate solution.
- Place two carbon (graphite) electrodes into the solution, connected to a DC power supply.
- Turn on the power supply and observe what happens at each electrode.
- After a set time, examine the electrodes.
Key Observations
| Electrode | Observation | Explanation |
|---|
| Cathode (negative) | Copper metal deposited (pinkish-brown coating) | Cu²⁺ ions gain electrons (reduction): Cu²⁺ + 2e⁻ → Cu |
| Anode (positive) | Bubbles of gas (oxygen) | Water molecules lose electrons (oxidation): 2H₂O → O₂ + 4H⁺ + 4e⁻ |
Variables
| Variable type | Variable |
|---|
| Independent variable (IV) | Depends on the investigation (e.g. concentration of solution, current) |
| Dependent variable (DV) | Mass of metal deposited or volume of gas produced |
| Control variables | Volume of solution, size of electrodes, time, temperature |
Key Rules for Electrolysis of Aqueous Solutions
- At the cathode: the least reactive metal ion is discharged (metal deposited). If the metal is more reactive than hydrogen, hydrogen gas is produced instead.
- At the anode: if the solution contains a halide (Cl⁻, Br⁻, I⁻), the halogen is produced. Otherwise, oxygen is produced from water.
Exam Tip: Learn the cathode/anode rules carefully. A common question is: "Predict what is produced at each electrode during the electrolysis of sodium chloride solution." Answer: hydrogen at cathode (sodium is more reactive), chlorine at anode (halide present).
Safety
- Wear eye protection.
- Good ventilation (chlorine or oxygen may be produced).
- Do not touch electrodes while the circuit is on.
Core Practical 7: Investigating Rates of Reaction
Aim
To investigate how changing the concentration of a reactant affects the rate of reaction, for example the reaction between sodium thiosulfate and hydrochloric acid.
Method