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Specimen lab book: Making salts
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Study Hack Lab
RP 1 · Chemistry
Making salts
Lab book
Name
Specimen
Date
2 November 2026
Course
GCSE Chemistry
Board and specification
AQA GCSE Chemistry (8462), 4.4.2.3AQA GCSE Combined Science: Trilogy (8464), 5.4.2.3Apparatus and techniques: AT 2, AT 3, AT 4, AT 6
Run
C29HO
Status
Finished: every stage done
Exam questions
30/30 marks
Aim
Make a pure, dry sample of copper(II) sulfate crystals from copper(II) oxide and dilute sulfuric acid, and work out your percentage yield.
Contents
Plan and risk assessment
Apparatus
Method
Results
Graph
Analysis
Conclusion and evaluation
Make safe and clear up
Exam questions on your data
Simulated data produced by Study Hack Lab from the student's own run (seed 20261004). Every reading, value and mark here is from that run; nothing has been retyped. Layout v1, practical v2. Original material; not affiliated with AQA, which has not reviewed it.
1 Plan and risk assessment
A metal oxide is a base: it neutralises an acid to make a salt and water. Copper(II) oxide is insoluble, so you add it until some is left over (in excess), filter that off, and crystallise the blue copper(II) sulfate from the solution.
CuO(s) + H₂SO₄(aq) → CuSO₄(aq) + H₂O(l)
Variables
Independent (you change)
None: this is a preparation, not an investigation
Dependent (you measure)
Mass of dry crystals in g
Control (you keep the same)
Volume and concentration of the acid; Copper(II) oxide in excess; How far the solution is evaporated
Prediction
What colour will the solution be once the black copper(II) oxide has reacted with the acid?
BlueRight first time
Copper(II) sulfate solution is blue. The black colour belongs to the solid copper(II) oxide, which disappears as it reacts.
Which reactant should be in excess at the end, and why?
Copper(II) oxide: then all the acid reacts, and the extra solid can be filtered off.Right first time
Copper(II) oxide is insoluble, so any extra is easy to remove by filtering. Extra acid would stay in the solution and end up in the crystals. You cannot see when you have exactly the right amount.
Will you get all the crystals the acid could make (a 100 % yield)?
No: some copper(II) sulfate stays dissolved in the solution, and some is lost along the way.Right first time
Your yield was 45 %. Crystals only form from the copper(II) sulfate that cannot stay dissolved. The rest stays in the solution left in the dish, and a little is lost on the filter paper and the glassware.
Risk assessment
Hazard
Harm it could cause
Control you chose
Hot dilute sulfuric acid (1.0 mol/dm³, irritant)
Irritates the eyes and skin; hot acid splashing into the eyes can damage them
Wear goggles; heat the acid only until it is almost boiling, then turn the Bunsen off.Right first time
Hot acid frothing up when the oxide is added
Hot acid splashes onto skin or into eyes
Add the copper(II) oxide a small spatula at a time, stirring.Right first time
Copper(II) oxide powder (harmful)
Harmful if swallowed; the dust irritates the eyes and lungs
Use a spatula, do not raise dust, and wash your hands afterwards.Right first time
Copper(II) sulfate (harmful; toxic to water life)
Harmful if swallowed; irritates the eyes and skin
Hand the crystals in for recycling; never take them home or pour solutions down the sink.Right first time
Bunsen flame and the hot tripod, gauze and basin
Burns; hair or paper catching fire
Tie long hair back, use the yellow safety flame when not heating, and let things cool before moving them.Right first time
Solution heated to dryness
Hot solid spits into the eyes; the basin can crack
Heat on a water bath and stop when about half of the solution is left.Right first time
2 Apparatus
✓Safety goggles Protect your eyes from hot acid.
✓Dilute sulfuric acid, 1.0 mol/dm³ (irritant) The acid: 40 cm³ makes the salt.
✓100 cm³ beaker and glass rod The reaction happens here; stir with the rod.
✓Bunsen burner, tripod, gauze and heatproof mat Warms the acid (and could heat the basin).
✓Copper(II) oxide powder (harmful), spatula and weighing boat The insoluble base, added until in excess.
✓Top-pan balance (resolution 0.01 g) Weighs the copper(II) oxide and the crystals.
✓Filter funnel, filter paper, clamp stand and conical flask Removes the excess copper(II) oxide.
✓Evaporating basin on a water bath (250 cm³ beaker) Evaporates water gently to the crystallisation point.
✓Crystallising dish The crystals grow here as the solution cools.
✓Watch glass and filter paper Dry and weigh the crystals.
3 Method: your choices
Which version are you doing?: AQA required practical 1: a soluble salt, copper(II) sulfate crystalsCopper(II) oxide and warm sulfuric acid, filter, evaporate on a water bath and crystallise; a percentage yield.
Put on safety gogglesSafety: DoneHot acid can spit or froth into your eyes, and long hair can catch in a Bunsen flame.
Warm the acid: DoneThe copper(II) oxide reacts much faster with warm acid. Do not boil it: hot acid spits.
Add the copper(II) oxide: A small spatula at a time, stirring with the glass rodEach portion reacts before the next goes in. No frothing.
Decide when to stop adding: When some black powder stays at the bottom, however much I stirThe copper(II) oxide is in excess, so all the acid has reacted. The extra solid is filtered off.
Filter the mixture: Slowly, down the glass rod, keeping the liquid below the top of the paperA clear blue filtrate. A little solution stays soaked in the paper.
Concentrate the solution: On the water bath, until about half of the solution is leftThe solution reaches the crystallisation point. Blue crystals grow as it cools.
Leave it to crystallise: Leave it in a cool place for 24 hoursSlow cooling (and a little more evaporation) grows large, regular blue crystals, 3–8 mm across, that are easy to dry.
Dry the crystals: DoneSolution clinging to the crystals adds to their mass and leaves impurities as it dries.
4 Results
9 of 9 readings taken.
The acid · Label on the bottle: 1.0 mol/dm³ sulfuric acid.
Reagent
Volume of sulfuric acid in cm³
Dilute sulfuric acid
40
The copper(II) oxide
Weighing
Mass of copper(II) oxide in g
Weighed out
4.06
Left on the boat
0.37
Added to the acid
3.69
Observations
Stage
Observation
Adding copper(II) oxide
The black powder disappears and the colourless acid turns blue. In the end some black powder stays at the bottom however much you stir.
Filtering
A clear blue solution drips into the flask. The black solid stays on the filter paper.
Crystallising
Large blue crystals with flat faces and sharp edges, in a little blue solution.
Weighing the crystals · Weigh twice: if the two masses agree, the crystals are dry.
Weighing
Mass of watch glass in g
Mass of watch glass and crystals in g
Mass of crystals in g
First
33.32
37.78
4.46
Check
33.32
37.77
4.45
Dry mass used
4.46
Yield
Maximum theoretical mass of crystals in g
Percentage yield in %
9.98
45
Anomaly: No anomalous reading.
5 Graph
This practical has no graph: the results are in the table above.
6 Analysis
Moles of acid (Higher)
moles = concentration (mol/dm³) × volume (dm³)
Calculate the number of moles of sulfuric acid you used.
0.040 molRight first time
Copper(II) oxide that reacts
mass = moles × Mr
One mole of copper(II) oxide reacts with one mole of sulfuric acid. Calculate the mass of copper(II) oxide that reacts with all your acid.
3.18 gRight first time
Copper(II) oxide you added
mass added = mass weighed out − mass left on the boat
Calculate the mass of copper(II) oxide you added to the acid.
3.69 gRight first time
Was it in excess?
You added 3.69 g of copper(II) oxide, and 3.18 g reacts with all your acid. Was the copper(II) oxide in excess?
Yes: I added more than reacts with all the acid.Right first time
Maximum mass of crystals
mass = moles × Mr
One mole of acid makes one mole of copper(II) sulfate crystals, CuSO₄·5H₂O. Calculate the maximum mass of crystals your acid could make.
9.98 gRight first time
Mass of crystals
mass of crystals = mass of watch glass and crystals − mass of watch glass
Calculate the mass of your dry crystals. If both weighings are used, take their mean first.
4.46 gRight first time
Percentage yield (Chemistry only)
percentage yield = mass of product made ÷ maximum theoretical mass × 100
Calculate your percentage yield.
45 %Right first time
7 Conclusion and evaluation
Quantity
Your value
Accepted value
Percentage yield (careful technique on the same acid)
45 %
44 %
Mass of dry crystals (careful technique)
4.46 g
4.44 g
Conclusion
Look at your product and your observations. What did you make?
Pure, dry blue crystals of copper(II) sulfateRight first time
One colour, regular blue crystals, nothing black in them, and all the acid reacted: a pure, dry sample.
Sources of error
Copper(II) sulfate left dissolved in the solution in the dish: systematic or random?
SystematicRight first time
Crystals only form from the salt that cannot stay dissolved, so the mass of crystals and the yield are always lower than the theoretical maximum.
Solution left in the filter paper and on the beaker and basin: systematic or random?
SystematicRight first time
Salt that never reaches the dish cannot crystallise, so the yield is lower.
Crystals still wet when weighed: systematic or random?
SystematicRight first time
The solution on them adds mass, so the mass of crystals and the yield come out too high (even over 100 %).
Acid left unreacted (cold acid, or stopping before solid stayed): systematic or random?
SystematicRight first time
Less copper(II) sulfate is made, so the yield is lower, and the left-over acid makes the crystals impure.
The mixture frothing over the top of the beaker: systematic or random?
SystematicRight first time
Solution lost over the side takes salt with it, so the yield is lower.
Black copper(II) oxide getting through the filter: systematic or random?
SystematicRight first time
The crystals are not pure, and the black specks add a little mass.
Heating the solution to dryness: systematic or random?
SystematicRight first time
The salt spits out and loses its water of crystallisation, so the product is a white-blue powder, not the blue crystals, and its mass cannot be compared with the theoretical mass of crystals.
How much water was evaporated (“about half”) and how warm the room was: systematic or random?
RandomRight first time
Each group evaporates a different amount and leaves its dish somewhere a little warmer or cooler, so yields spread out across the class.
Improvement
Which change would most improve your results?
Rinse the filter paper and the glassware with a little distilled water into the filtrate.Right first time
Repeatable or reproducible
You make a second batch the same way, with the same apparatus, and get almost the same mass of crystals. This shows your method is…
RepeatableRight first time
Repeatable: the same person, method and equipment give similar results.
Another group, using an electric heater instead of a water bath, gets a similar percentage yield. This shows the result is…
ReproducibleRight first time
Reproducible: a different person or a different method gives similar results.
8 Make safe and clear up
Turn off the Bunsen burner and the gas tap
Leave the tripod, gauze and basin to cool on the mat before you move them
Put the filter paper with the black copper(II) oxide in the solid waste bin
Hand your crystals in for recycling: not down the sink, and not home
Wash the glassware, wipe the bench and wash your hands
9 Exam questions on your data
On your own readings, self-marked against the mark scheme, with error carried forward where it applies. Total 30/30.
01.1[2 marks]
A student made copper(II) sulfate from copper(II) oxide and dilute sulfuric acid.
Complete the balanced equation for the reaction. Include state symbols.
CuO(s) + H₂SO₄(aq) → ________ + ________
Your answer
CuSO4(aq) + H2O(l)
2/2 self-marked
CuSO₄ and H₂O (correct formulae)
State symbols: CuSO₄(aq) and H₂O(l)
Self-marked: 2 of 2 marks. This is your own judgement against the mark scheme.
Model answer: CuO(s) + H₂SO₄(aq) → CuSO₄(aq) + H₂O(l)
01.2[1 mark]
You warmed the acid before adding the copper(II) oxide.
Why is the sulfuric acid warmed before the copper(II) oxide is added?
Tick (✓) one box.
✓ To make the reaction faster (your choice)
To make more copper(II) sulfate
To evaporate the water from the acid
To make the acid less hazardous
Your answer
To make the reaction faster
1/1
To make the reaction faster
Full marks. Clear and precise.
Model answer: To make the reaction faster (to speed up the reaction).
01.3[2 marks]
The dilute sulfuric acid is heated until it is almost boiling.
Suggest one safety precaution the student should take when heating the acid. Give a reason for your answer.
Your answer
Wear safety goggles because hot acid could splash into your eyes and damage them.
2/2 self-marked
A precaution: wear goggles (eye protection); do not let the acid boil; turn the Bunsen off before adding the oxide; add the oxide in small portions; tie hair back
Linked reason: hot acid could splash or spit (into the eyes) and burn or damage them (the acid is an irritant)
Self-marked: 2 of 2 marks. This is your own judgement against the mark scheme.
Model answer: Wear safety goggles, because the hot acid could spit or splash into the eyes and damage them.
01.4[1 mark]
The student added copper(II) oxide to the warm acid a little at a time, stirring after each addition.
How would the student know when the copper(II) oxide was in excess?
Your answer
Black solid remains at the bottom of the beaker and no longer disappears when stirred.
1/1 self-marked
(Black) solid remains / no longer disappears (allow copper(II) oxide stays at the bottom)
Self-marked: 1 of 1 mark. This is your own judgement against the mark scheme.
Model answer: Some black solid (copper(II) oxide) stays at the bottom of the beaker and does not disappear when stirred.
01.5[2 marks]
Explain why copper(II) oxide is added until it is in excess.
Your answer
To make sure all the acid reacts. The excess copper oxide is insoluble so it can be filtered off.
2/2 self-marked
So that all the acid reacts (is used up / neutralised)
The excess (insoluble) solid can be removed by filtering
Self-marked: 2 of 2 marks. This is your own judgement against the mark scheme.
Model answer: So that all of the acid reacts (none is left in the solution), and the excess copper(II) oxide is insoluble so it can be removed by filtering.
01.6[1 mark]
Why is the mixture filtered?
Your answer
To remove the excess copper(II) oxide.
1/1 self-marked
To remove the excess (unreacted) copper(II) oxide (ignore “to remove impurities”)
Self-marked: 1 of 1 mark. This is your own judgement against the mark scheme.
Model answer: To remove the excess (unreacted) copper(II) oxide.
01.7[1 mark]
A student made copper(II) sulfate by adding copper(II) oxide to warm dilute sulfuric acid until no more would react.
Name one other copper compound that could be added to sulfuric acid to make copper(II) sulfate.
Your answer
copper carbonate
1/1 self-marked
Copper(II) carbonate or copper(II) hydroxide (allow CuCO₃ or Cu(OH)₂; do not accept copper, or another salt such as copper chloride)
Self-marked: 1 of 1 mark. This is your own judgement against the mark scheme.
Model answer: Copper(II) carbonate (or copper(II) hydroxide).
02.1[2 marks]
After filtering, the student has a blue solution of copper(II) sulfate.
Describe how the student should get copper(II) sulfate crystals from the solution.
Your answer
Heat the solution on a water bath to evaporate some of the water until crystals start to form. Then leave it to cool and crystallise.
2/2 self-marked
Heat the solution to evaporate some of the water / until the crystallisation point is reached (do not accept evaporating the acid or the salt, or heating to dryness)
Leave the solution to cool / to crystallise
Self-marked: 2 of 2 marks. This is your own judgement against the mark scheme.
Model answer: Heat the solution (on a water bath) to evaporate some of the water until the crystallisation point is reached. Then leave the solution to cool so that crystals form.
02.2[1 mark]
The student heated the solution in an evaporating basin on a water bath.
Give one reason why a water bath is used to heat the solution, rather than heating it directly with a Bunsen burner.
Your answer
It heats the solution gently and cannot go above 100 °C so the solution does not spit.
1/1 self-marked
It heats gently / cannot go above 100 °C, so the solution does not spit, boil dry, or the crystals do not break down (lose their water)
Self-marked: 1 of 1 mark. This is your own judgement against the mark scheme.
Model answer: The water bath heats the solution gently (it cannot go above 100 °C), so it does not spit or boil dry and the crystals are not decomposed.
02.3[1 mark]
Another student wants to grow larger crystals.
What should the student do?
Tick (✓) one box.
Cool the solution quickly in iced water
✓ Leave the solution to cool slowly (your choice)
Evaporate the solution to dryness
Add more copper(II) oxide to the acid
Your answer
Leave the solution to cool slowly
1/1
Leave the solution to cool slowly
Full marks. Clear and precise.
Model answer: Leave the solution to cool slowly.
02.4[3 marks]
You used 40 cm³ of 1.0 mol/dm³ sulfuric acid.
One mole of sulfuric acid makes one mole of copper(II) sulfate crystals, CuSO₄·5H₂O.
Relative formula mass (Mr) of CuSO₄·5H₂O: 249.5
GCSE Chemistry only, Higher tier.
Calculate the maximum mass of copper(II) sulfate crystals that could be made.
Your answer
9.98
Working: moles of acid = 1.0 × 40 ÷ 1000 = 0.04 mol
mass = 0.04 × 249.5
mass = 9.98 g
3/3
Moles of acid = 1.0 × 40 ÷ 1000 = 0.04 mol
Mass = moles × 249.5
Maximum mass = 9.98 g
Full marks. That is exactly what the mark scheme is looking for.
Model answer: moles of acid = 1.0 × 40 ÷ 1000 = 0.04 mol
mass = 0.04 × 249.5
mass = 9.98 g
02.5[3 marks]
Table 1 shows the masses you recorded for your dry crystals.
Table 1
Mass of watch glass in g
Mass of watch glass and dry crystals in g
33.32
37.77
GCSE Chemistry only, Higher tier.
Calculate your percentage yield of copper(II) sulfate crystals.
Use your answer to the previous question.
Your answer
44.6
Working: mass of crystals = 37.77 − 33.32 = 4.45 g
percentage yield = 4.45 ÷ 9.98 × 100
percentage yield = 44.6 %
3/3
Mass of crystals = 37.77 − 33.32 = 4.45 g
4.45 ÷ 9.98 × 100 (allow their maximum mass)
Percentage yield = 44.6 % (allow an answer consistent with their maximum mass)
Full marks. Clear and precise.
Model answer: mass of crystals = 37.77 − 33.32 = 4.45 g
percentage yield = 4.45 ÷ 9.98 × 100
percentage yield = 44.6 %
02.6[1 mark]
Every group in the class made copper(II) sulfate crystals from 40 cm³ of the same acid. The maximum mass of crystals was 9.98 g.
Table 2 shows the class results.
Which result is anomalous?
Select one row.
Table 2
Group
Mass of crystals in g
Percentage yield in %
You
4.45
45
A
4.89
49
B
4.49
45
C
6.19
62
D
4.29
43
E
10.68
107
Your answer
group E
1/1
Group E: a yield above 100 %
Full marks. Your answer meets all the points for this question. Group E’s yield is over 100 %: more crystals than the acid could possibly make.
Model answer: Group E. Its yield is over 100 %, which is impossible.
02.7[1 mark]
Suggest why group E’s percentage yield is more than 100 %.
Your answer
The crystals were still wet when they were weighed.
1/1 self-marked
The crystals were still wet (not dried) when they were weighed (allow contained water or solution)
Self-marked: 1 of 1 mark. This is your own judgement against the mark scheme.
Model answer: The crystals were still wet when they were weighed, so the solution on them added to their mass.
02.8[2 marks]
Give two reasons why the percentage yield of dry crystals is less than 100 %.
Your answer
Some copper sulfate stays dissolved in the solution and does not crystallise. Some solution is lost on the filter paper and left in the beaker.
2/2 self-marked
Some copper(II) sulfate stays dissolved in the solution (not all of it crystallises)
Some solution or crystals are lost: left on the filter paper or glassware, or lost when transferring
Not all the crystals were collected (some left in the dish or lost when drying)
Self-marked: 2 of 2 marks. This is your own judgement against the mark scheme.
Model answer: Some copper(II) sulfate stays dissolved in the solution left in the dish. Some solution is lost on the filter paper and the glassware.
03[6 marks]
Magnesium sulfate is a soluble salt. It can be made from magnesium oxide, which is insoluble, and dilute sulfuric acid.
Describe a method to make pure, dry crystals of magnesium sulfate from magnesium oxide and dilute sulfuric acid.
Your answer
1. Measure about 40 cm³ of dilute sulfuric acid into a beaker.
2. Warm the acid gently with a Bunsen burner, then turn it off.
3. Add magnesium oxide a little at a time, stirring with a glass rod.
4. Keep adding until the magnesium oxide is in excess: some solid stays and does not disappear.
5. Filter the mixture with a filter funnel and filter paper to remove the excess magnesium oxide.
6. Heat the filtrate in an evaporating basin on a water bath to evaporate some of the water, until the crystallisation point.
7. Leave the solution to cool and crystallise.
8. Remove the crystals and pat them dry with filter paper.
6/6 self-marked
Put dilute sulfuric acid in a beaker (measure a volume)
Warm the acid
Add magnesium oxide (a little at a time) and stir
Until the magnesium oxide is in excess / solid remains
Filter (with filter paper and funnel) to remove the excess magnesium oxide
Heat the solution (in an evaporating basin, on a water bath or electric heater) to evaporate some water / to the crystallisation point
Leave to cool and crystallise
Pat the crystals dry with filter paper (or leave in a warm place to dry)
Self-marked: Level 3, 6 of 6 marks. You ticked 8 of 8 indicative points. This is your own judgement against the mark scheme.
Model answer: 1. Measure about 40 cm³ of dilute sulfuric acid into a beaker.
2. Warm the acid gently with a Bunsen burner, then turn it off.
3. Add magnesium oxide a little at a time, stirring with a glass rod.
4. Keep adding until the magnesium oxide is in excess: some solid stays and does not disappear.
5. Filter the mixture with a filter funnel and filter paper to remove the excess magnesium oxide.
6. Heat the filtrate in an evaporating basin on a water bath to evaporate some of the water, until the crystallisation point.
7. Leave the solution to cool and crystallise.
8. Remove the crystals and pat them dry with filter paper.
Unseen data: the same skills, new apparatus
01[2 marks]
A student makes magnesium sulfate crystals. The empty evaporating dish has a mass of 31.06 g. The crystals are dried in a warm oven and weighed in the dish every 10 minutes.
Mass of evaporating dish and crystals while drying
Weighing
Mass in g
1
35.67
2
35.39
3
35.22
4
35.19
5
35.19
Calculate the mass of the dry magnesium sulfate crystals.
Your answer
4.13
Working: 35.19 - 31.06
2/2
Uses the constant mass, 35.19 g.
Subtracts the dish: the dry crystals in g.
Full marks. Your answer meets all the points for this question.
Model answer: The mass stopped changing at 35.19 g (weighings 4 and 5 agree), so the crystals are dry.
Mass of crystals = 35.19 − 31.06 = 4.13 g.
02[2 marks]
A student has a filtered solution of zinc chloride, made from zinc oxide and dilute hydrochloric acid. They want pure, dry crystals of zinc chloride.
Which TWO steps should they do? Tick (✓) two boxes.
✓ Heat the solution in an evaporating basin on a water bath until crystals start to form, then leave it to cool. (your choice)
✓ Filter off the crystals and pat them dry between pieces of filter paper. (your choice)
Heat the solution strongly with a Bunsen burner until all the liquid has gone.
Heat the solution to boil off the hydrochloric acid, leaving the zinc chloride behind.
Weigh the crystals straight from the solution, so that none are lost.
Your answer
Heat the solution in an evaporating basin on a water bath until crystals start to form, then leave it to cool.; Filter off the crystals and pat them dry between pieces of filter paper.
2/2
Heat the solution in an evaporating basin on a water bath until crystals start to form, then leave it to cool.
Filter off the crystals and pat them dry between pieces of filter paper.
Full marks. That is exactly what the mark scheme is looking for.
Model answer: Gentle heating (a water bath or an electric heater) evaporates some of the water until the solution reaches its crystallisation point; crystals grow as it cools. Filter them off and pat them dry. Strong heating to dryness can decompose the salt or drive off its water of crystallisation; it is the water that evaporates, not the acid.
03[2 marks]
A student makes nickel(II) chloride solution by adding green nickel(II) carbonate powder, a spatula at a time, to dilute hydrochloric acid. Bubbles of carbon dioxide form as it reacts.
Which TWO statements are correct? Tick (✓) two boxes.
✓ The nickel(II) carbonate is in excess when green solid stays in the beaker however much it is stirred, and no more bubbles form. (your choice)
✓ Using an excess makes sure all the acid reacts; the extra solid can then be filtered off. (your choice)
The nickel(II) carbonate is in excess as soon as the solution turns green.
Using an excess makes the crystals grow larger.
The extra nickel(II) carbonate removes impurities from the acid.
Your answer
The nickel(II) carbonate is in excess when green solid stays in the beaker however much it is stirred, and no more bubbles form.; Using an excess makes sure all the acid reacts; the extra solid can then be filtered off.
2/2
The nickel(II) carbonate is in excess when green solid stays in the beaker however much it is stirred, and no more bubbles form.
Using an excess makes sure all the acid reacts; the extra solid can then be filtered off.
Full marks. Your answer meets all the points for this question.
Model answer: Solid that stays and no more fizzing are visible signs that no acid is left to react. The excess makes sure all the acid is used up, and being insoluble it is easily filtered off. The solution turns green as soon as some carbonate reacts, long before the acid is used up.