Chemistry 5070/32 — October/November 2024
Cambridge O-Level · Practical Test · worked solutions for every part, with the mark scheme
Topics Use of Techniques, Apparatus and Materials · Observations and Measurements · Experimental Contexts · Analysis, Conclusions and Evaluation · Qualitative Analysis · Planning Experiments and Investigations
You are provided with:
- dilute hydrochloric acid, , X
- of an aqueous solution of sodium carbonate, Y.
You are going to investigate the reaction between X and Y.
Read all the instructions carefully before starting the experiments.
Instructions
You are going to do four titration experiments.
Rinse and fill a burette with X.
Experiment 1
- Use a volumetric pipette to add of Y to a conical flask.
- Add five drops of methyl orange indicator to the conical flask.
- Place the conical flask on a white tile.
- Record the initial burette reading in Table 1.1.
- Add X from the burette while swirling the flask, adding drop by drop near the end-point, until the solution just changes colour.
- Record the final burette reading in Table 1.1.
Experiments 2, 3 and 4
- Empty the conical flask and rinse it with distilled water.
- Refill the burette if necessary.
- Repeat Experiment 1.
Calculate the volume used in each experiment and record your values in Table 1.1.
Table 1.1
| experiment number 1 | 2 | 3 | 4 | |
|---|---|---|---|---|
| final burette reading / | ||||
| initial burette reading / | ||||
| volume of X used / | ||||
| best titration results () |
Answer
- Complete all four initial and final burette readings in Table 1.1.
- Record every reading and every calculated volume to 1 decimal place, including a final 0.0 where appropriate.
- Calculate each volume used using:
- Enter the four volumes in the third row of Table 1.1.
- The readings should be close to the supervisor's values.
Completed Table 1.1 with all readings and volumes used, each to 1 decimal place; volume used = final reading - initial reading.
Walkthrough
This part is about taking and recording burette readings correctly. Each experiment gives a final and an initial burette reading. The volume of acid X used is found by subtracting the initial reading from the final reading. All readings and calculated volumes must be recorded to 1 decimal place, so a reading of exactly 25 cm3 must be written as 25.0, and an initial reading of exactly zero must be written as 0.0. The four experiments give four volumes; these should be close to one another and to the supervisor's value.
Key Takeaways
- Burette readings are recorded to 1 decimal place.
- Volume used = final reading - initial reading.
- Repeating the titration allows a reliable average to be calculated.
Common Mistakes
- Writing readings without a decimal place, such as 25 instead of 25.0.
- Writing 0 instead of 0.0 for an initial reading.
- Forgetting to calculate the volume used for each experiment.
- Recording readings in the wrong row of the table.
Things to Be Careful About
- Keep the same precision (1 decimal place) for every reading and every calculated volume.
- Use the correct units, cm3, for all volumes.
- Make sure the final reading is larger than the initial reading for each experiment.
Answer
- Tick the two volumes that are closest to each other.
- The two ticked results are concordant: they are within 0.2 cm3 of each other.
The two concordant volumes (within 0.2 cm3 of each other) are ticked.
Walkthrough
Look at the four volumes of X used. The two best results are the two that agree most closely with each other. Tick exactly these two in Table 1.1. The explanation should state that the two chosen volumes are concordant, meaning they are within 0.2 cm3 of each other. This shows the results are reliable and can be averaged.
Key Takeaways
- Concordant results are those that agree closely.
- Only the two best results should be used to calculate the average.
Common Mistakes
- Ticking three results instead of two.
- Ticking an anomalous result that is far from the others.
- Giving no explanation for the choice.
Things to Be Careful About
- The mark scheme requires exactly two ticks.
- The explanation must mention concordance or the 0.2 cm3 agreement.
Use the ticked () titration results in Table 1.1 to calculate the average volume of X needed to neutralise of Y.
volume = ______
Working
Let the two ticked volumes be and .
Answer
Average volume = (sum of the two ticked volumes) ÷ 2, in cm3.
Average of the two ticked volumes, in cm3.
Walkthrough
Use only the two volumes that were ticked in part (b). Add them together and divide by 2. This gives the average volume of X needed to neutralise 25.0 cm3 of Y. Do not include the other two volumes, because they are less reliable.
Key Takeaways
- The average is calculated from the concordant results only.
- The mean gives a more reliable value than any single titration.
Common Mistakes
- Averaging all four volumes instead of only the two ticked ones.
- Including an anomalous result in the average.
- Forgetting to divide by 2.
Things to Be Careful About
- Use exactly the two values ticked in part (b).
- Give the answer in cm3.
Use your answer from (c) to calculate the number of moles of in the average volume of X needed to neutralise of Y.
number of moles = ______
Working
Answer
Moles of HCl = (average volume from (c) ÷ 1000) × 0.500 mol.
Moles of HCl = (average volume in cm3 / 1000) × 0.500.
Walkthrough
The concentration of X is 0.500 mol / dm3. To find moles, the volume must be in dm3, so divide the average volume in cm3 by 1000. Then multiply by the concentration. This gives the number of moles of HCl in the average volume used.
Key Takeaways
- Moles = concentration × volume (in dm3).
- To convert cm3 to dm3, divide by 1000.
Common Mistakes
- Forgetting to divide the volume by 1000.
- Using the wrong concentration.
- Mixing up cm3 and dm3.
Things to Be Careful About
- The volume must be in dm3 before multiplying by the concentration.
- The answer is in moles.
The equation for the reaction between hydrochloric acid and sodium carbonate is shown.
Use your answer from (d) to calculate the concentration of sodium carbonate in Y.
Give your answer to three significant figures.
concentration = ______
Working
From the equation, 2 mol HCl react with 1 mol .
M1: moles of in 25.0 cm3 of Y = moles of HCl from (d) ÷ 2.
M2: concentration of Y = moles of ÷ (25.0/1000)
M3: Give the answer to 3 significant figures.
Answer
Concentration of Y = (moles of HCl from (d) ÷ 2) × 1000/25, in mol / dm3, to 3 s.f.
Concentration of Y = (moles HCl from (d) / 2) × 1000/25 mol / dm3, to 3 s.f.
Walkthrough
The balanced equation shows that 2 mol of HCl react with 1 mol of Na2CO3. So the moles of Na2CO3 in the 25.0 cm3 sample are half the moles of HCl found in part (d). The concentration is then moles divided by volume in dm3; 25.0 cm3 is 25.0/1000 dm3. Finally, round the answer to 3 significant figures.
Key Takeaways
- Use the mole ratio from the balanced equation.
- Concentration = moles ÷ volume in dm3.
- Round only at the end, to 3 significant figures.
Common Mistakes
- Forgetting to divide the moles of HCl by 2.
- Using 25.0 cm3 without converting to dm3.
- Rounding before the final step.
Things to Be Careful About
- The volume of Y is 25.0 cm3, not 150 cm3.
- The answer must be given to 3 significant figures with units mol / dm3.
Use your answer to (e) to calculate the mass of in of Y.
[: , 12; , 16; , 23]
mass = ______
Working
M1:
M2: moles of in 150 cm3 of Y = concentration from (e) × 150/1000
M3: mass = moles × 106
Answer
Mass of in 150 cm3 of Y = (concentration from (e) × 0.150) × 106 g.
Mass of Na2CO3 in 150 cm3 of Y = (concentration from (e) × 0.150) × 106 g.
Walkthrough
First calculate the relative molecular mass of sodium carbonate: 2 × 23 for sodium, plus 12 for carbon, plus 3 × 16 for oxygen, giving 106. Then find the number of moles of Na2CO3 in 150 cm3 of Y by multiplying the concentration from part (e) by 150/1000 (since 150 cm3 = 0.150 dm3). Finally multiply the moles by the M_r to get the mass in grams.
Key Takeaways
- M_r is found by adding the relative atomic masses of all atoms in the formula.
- Moles = concentration × volume in dm3.
- Mass = moles × M_r.
Common Mistakes
- Using 25.0 cm3 instead of 150 cm3.
- Using the wrong M_r for Na2CO3.
- Forgetting to convert 150 cm3 to dm3.
Things to Be Careful About
- 150 cm3 = 0.150 dm3.
- The final answer must be in grams.
Answer
To mix the contents of the flask thoroughly so the acid and carbonate react evenly and the end-point is reliable.
To mix the contents thoroughly.
Walkthrough
Swirling the conical flask while acid is added mixes the reactants thoroughly. This ensures the acid and carbonate react evenly and that the colour change at the end-point is reliable. Without swirling, local excess of acid could give a false end-point.
Key Takeaways
- Swirling ensures thorough mixing during a titration.
- It helps give an accurate end-point.
Common Mistakes
- Saying swirling cools the mixture.
- Saying swirling makes the reaction faster without mentioning mixing.
Things to Be Careful About
- The mark scheme accepts 'to mix the contents thoroughly/evenly'.
Answer
To make sure the end-point is not exceeded, so the volume of acid added is accurate.
To avoid overshooting the end-point, so the volume is accurate.
Walkthrough
Near the end-point the colour change happens with a single drop. Adding the acid drop by drop lets the candidate stop exactly when the colour just changes, so the end-point is not overshot. This gives an accurate volume of acid used.
Key Takeaways
- Dropwise addition near the end-point prevents overshooting.
- The end-point is the first permanent colour change.
Common Mistakes
- Saying dropwise addition makes the titration faster.
- Saying it cools the solution.
Things to Be Careful About
- The mark scheme accepts 'to ensure the end-point is not exceeded' or 'so the volume is accurate'.
You are provided with solution P and solution Q.
You will do a series of tests on P and Q.
Tests on solution P
You should:
- record your observations for each of these tests
- test and identify any gases evolved
- describe the gas test used that identifies any gas evolved.
Answer
yellow
yellow
Walkthrough
When conducting a flame test on an unknown sample containing sodium ions (), the characteristic persistent yellow (or yellow-orange) flame is observed.
Key Takeaways
- gives a yellow flame in a flame test.
- Other common flame test colours to recall at O Level: (red), (lilac), (orange-red), (blue-green), (apple-green).
Common Mistakes
- Confusing the yellow flame of sodium with the lilac flame of potassium or orange-red of calcium.
Things to Be Careful About
- Ensure the flame colour recorded matches the standard syllabus descriptors.
Answer
sodium (or )
sodium
Walkthrough
A yellow flame test result indicates the presence of sodium ions ().
Key Takeaways
- Cations can be deduced directly from their characteristic flame colours.
Common Mistakes
- Writing an incorrect charge for the ion (e.g. ).
Things to Be Careful About
- Either the full name 'sodium' or the correct chemical formula '' is accepted.
To depth of P in a boiling tube, add depth of aqueous sodium hydroxide.
Add a piece of aluminium foil and warm the mixture carefully.
______
Answer
- Gas tested with damp red litmus paper
- Litmus paper turns blue
- Gas is ammonia ()
Damp red litmus turns blue; gas evolved is ammonia (NH3)
Walkthrough
Adding aqueous sodium hydroxide and aluminium foil to a solution followed by gentle warming is the standard qualitative test for nitrate ions (). In this reaction, nitrate ions are reduced by aluminium under alkaline conditions to produce ammonia gas ().
To earn all 3 marks:
- State the test reagent/medium used: damp red litmus paper.
- State the observed result: turns blue.
- Identify the evolved gas: ammonia ().
Key Takeaways
- Nitrate test: warm with aqueous and foil ammonia gas produced.
- Ammonia test: turns damp red litmus paper blue.
Common Mistakes
- Omitting that the litmus paper must be damp or moist.
- Naming the anion (nitrate) here instead of describing the gas test, observation, and the gas itself as prompted by the stem.
Things to Be Careful About
- The stem explicitly reminds candidates to test and identify any gases evolved and describe the test used.
Answer
nitrate (or )
nitrate
Walkthrough
The production of ammonia upon heating with aqueous sodium hydroxide and aluminium foil confirms the presence of nitrate ions ().
Key Takeaways
- reducing an unknown to is the specific qualitative test for nitrate ().
Common Mistakes
- Writing nitrite instead of nitrate.
Things to Be Careful About
- Both the name 'nitrate' and formula '' are acceptable.
Some gases have distinctive smells.
Suggest why gases should not be identified by smell.
______
Answer
The gas may be toxic (or poisonous / hazardous to health).
The gas may be toxic
Walkthrough
Many gases produced in chemical reactions (such as chlorine, sulfur dioxide, or ammonia) are toxic, irritant, or harmful when inhaled in significant amounts. Therefore, chemical and indicator tests must always be used instead of smelling unknown gases.
Key Takeaways
- Smelling unknown gases poses severe health and safety risks due to potential toxicity and irritation.
Common Mistakes
- Vague answers like 'it smells bad' or 'it is dangerous' without specifying toxicity/poisonous nature or respiratory irritation.
Things to Be Careful About
- Keep the answer crisp and focused on safety/toxicity.
Tests on solution Q
To depth of Q in a test-tube, add aqueous sodium hydroxide drop by drop until a change is seen.
Then add excess aqueous sodium hydroxide.
Record your observations.
______
Answer
- Green precipitate
- Soluble in excess (precipitate dissolves in excess)
- Giving a green solution
Green precipitate, soluble in excess to form a green solution
Walkthrough
For a solution containing chromium(III) ions ():
- On dropwise addition of aqueous sodium hydroxide, a grey-green (or green) precipitate of chromium(III) hydroxide, , forms.
- In excess aqueous sodium hydroxide, the amphoteric precipitate dissolves to form a green solution containing chromate(III) / tetrahydroxochromate(III) complex ions.
Key Takeaways
- with : green precipitate soluble in excess green solution.
- Compare with which forms a green precipitate insoluble in excess.
Common Mistakes
- Forgetting to state the colour of the solution formed in excess.
- Confusing with .
Things to Be Careful About
- All three points (precipitate colour, solubility in excess, and colour of final solution) must be stated clearly.
To depth of Q in a test-tube, add aqueous ammonia drop by drop until a change is seen.
Then add excess aqueous ammonia.
Record your observations.
______
Answer
- Green precipitate
- Insoluble in excess
Green precipitate, insoluble in excess
Walkthrough
When aqueous ammonia is added to a solution containing :
- A green (or grey-green) precipitate of forms.
- On adding excess aqueous ammonia, the precipitate remains insoluble (or is only very slightly soluble under specific conditions, but standard 5070 observation is insoluble in excess).
Key Takeaways
- with : green precipitate, insoluble in excess.
Common Mistakes
- Stating that it dissolves in excess ammonia.
Things to Be Careful About
- Distinguish clearly between behaviour with (soluble in excess) and with (insoluble in excess).
To depth of Q in a test-tube, add depth of dilute nitric acid.
Record your observations.
______
Then add aqueous silver nitrate drop by drop until a change is seen.
Record your observations.
______
Answer
With dilute nitric acid:
- No change / no reaction (no effervescence)
With aqueous silver nitrate:
- White precipitate forms
With nitric acid: no change; with silver nitrate: white precipitate
Walkthrough
- Adding dilute nitric acid to a solution containing chloride ions results in no observable change (no effervescence or precipitation, confirming the absence of carbonate or sulfite ions).
- Subsequent addition of aqueous silver nitrate results in a precipitation reaction between silver ions and chloride ions:
forming an insoluble white precipitate of silver chloride ().
Key Takeaways
- Acidification with dilute prevents false positives from carbonates.
- gives a white precipitate with , cream with , and yellow with .
Common Mistakes
- Leaving the first observation line blank instead of recording 'no change'.
- Writing 'white solution' instead of 'white precipitate'.
Things to Be Careful About
- Ensure 'precipitate' is explicitly written for the silver nitrate observation.
Answer
- cation: chromium(III) (or )
- anion: chloride (or )
cation = chromium(III), anion = chloride
Walkthrough
- Cation identification: In parts (f) and (g), solution Q gave a green precipitate with aqueous that dissolved in excess to a green solution, and a green precipitate with aqueous that was insoluble in excess. These observations uniquely identify the cation as chromium(III) ().
- Anion identification: In part (h), solution Q acidified with dilute nitric acid gave a white precipitate with aqueous silver nitrate, confirming the anion is chloride ().
Key Takeaways
- Green ppt soluble in excess (green solution) and insoluble in excess .
- White ppt with acidified .
Common Mistakes
- Omitting the oxidation state for the cation (writing just 'chromium' or 'iron(II)').
- Writing 'chlorine' instead of 'chloride'.
Things to Be Careful About
- State the oxidation state for transition metals with multiple oxidation states: chromium(III) / .
You are not expected to do any practical work for this question.
Muntz metal is an alloy that contains zinc and copper.
Zinc reacts with dilute sulfuric acid. Copper does not react with dilute sulfuric acid.
Plan an investigation to find the percentage by mass of zinc in a powdered sample of Muntz metal which contains only zinc and copper.
Your plan must include the use of common laboratory apparatus, Muntz metal and sulfuric acid. No other chemicals should be used.
Your plan must include:
- the apparatus needed
- the method to use and the measurements to take
- procedures to ensure that the percentage determined is as accurate as possible
- how the measurements are used to determine the percentage by mass of zinc in the sample of Muntz metal.
You may draw a diagram to help answer the question.
Answer
Apparatus
- balance
- beaker or conical flask
- measuring cylinder (for sulfuric acid)
- filter funnel and filter paper
- stirring rod
- optional: warm oven or drying apparatus
Method and measurements
- Weigh a known mass of powdered Muntz metal on a balance and record it.
- Put the powder in a beaker or conical flask.
- Add excess dilute sulfuric acid, in small portions, until no more effervescence is seen. Stir with a glass rod.
- Filter the mixture. The unreacted copper remains on the filter paper; the zinc sulfate solution passes through.
- Wash the copper with distilled water and dry it thoroughly.
- Weigh the dry copper and record its mass.
Accuracy
- Use excess sulfuric acid and wait until effervescence stops so all the zinc has reacted.
- Wash and dry the copper so no solution or water adds to its mass.
- Repeat the whole experiment and take an average.
Calculation
Mass of zinc = mass of Muntz metal - mass of copper.
or
Plan: weigh alloy, add excess sulfuric acid until effervescence stops, filter, wash and dry copper, weigh it, then % zinc = (mass alloy - mass copper) / mass alloy × 100%.
Walkthrough
This question asks you to plan an investigation, not to do it. The key chemistry is that zinc reacts with dilute sulfuric acid but copper does not. So adding excess acid to the alloy will dissolve/remove all the zinc as zinc sulfate solution and leave the copper as a solid. Filtration separates the solid copper from the solution. The difference between the original mass of alloy and the mass of recovered copper gives the mass of zinc. Dividing by the original mass and multiplying by 100 gives the percentage by mass.
The plan must cover four sections: apparatus, method and measurements, accuracy, and calculation. For apparatus, choose a container that can hold the reaction safely (beaker or conical flask), a balance for weighing, a measuring cylinder for the acid, and filtration apparatus (filter funnel and filter paper) to collect the copper. The method should be a clear sequence: weigh the alloy, add excess acid, wait until no more bubbles form, filter, wash and dry the copper, weigh it. The accuracy section should explain why excess acid is used (to make sure all zinc reacts), why the copper is washed and dried (to remove acid solution and water that would make its mass too high), and why repeats are averaged. Finally, the calculation uses the two measured masses.
Key Takeaways
- Zinc is more reactive than hydrogen, so it reacts with dilute sulfuric acid to give zinc sulfate and hydrogen. Copper is less reactive than hydrogen, so it does not react.
- A planning question needs a complete method: apparatus, procedure, measurements, accuracy, and calculation.
- Excess reagent and waiting for the reaction to finish ensure complete reaction.
- Filtration separates an insoluble solid from a solution.
- Percentage by mass is always (mass of component ÷ total mass of sample) × 100%.
Common Mistakes
- Not using excess sulfuric acid, or not waiting until effervescence stops, so some zinc remains unreacted and the copper mass is too high.
- Weighing the copper before it is dry; water adds extra mass.
- Forgetting to filter, so the copper cannot be separated from the zinc sulfate solution.
- Using the wrong formula, e.g. dividing by the mass of copper instead of the mass of the original alloy.
- Not repeating and averaging, which reduces the reliability of the result.
- Adding other chemicals, which is not allowed by the question.
Things to Be Careful About
- Record every mass with its unit, e.g. 2.00 g.
- Use excess acid and add it until no more effervescence is seen.
- Wash and dry the copper completely before the final weighing.
- In the calculation, keep the parentheses: percentage zinc = (mass of alloy − mass of copper) / mass of alloy × 100%.
- The mark scheme awards one mark from each section and any other two marks, so make sure all four sections are present.
- A labelled diagram of the filtration apparatus is optional; it can help show the method but is not essential.