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Chemistry · Edexcel 9CH0 · Paper 3: General and Practical Principles in Chemistry · June 2025

Edexcel A Level Chemistry Paper 3: General and Practical Principles in Chemistry June 2025 question paper 9CH0/03

2h 30m 120 marks

Edexcel 9CH0 · Paper 3

9 questions
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Question 1

This question is about ionisation energies.

The table shows the first four ionisation energies of three elements in the same group of the Periodic Table. The letters used are not the symbols of the elements.

ElementFirst ionisation energy / kJ mol−1Second ionisation energy / kJ mol−1Third ionisation energy / kJ mol−1Fourth ionisation energy / kJ mol−1
X403263239005080
Y419305144125877
Z496456369139544
(a)

State what is meant by the term ‘ first ionisation energy’.

(2)

Answer
Mark scheme for question 1(a)
(b)

Explain to which group the elements X, Y and Z belong.

(2)

Answer
Mark scheme for question 1(b)
(c)

Explain which of the elements X, Y and Z has the highest atomic number.

(3)

Answer
Mark scheme for question 1(c)

Question 2

This question is about compounds that contain both an alkene and an alcohol functional group.

(a)
Figure for question 2
(a)(i)

Describe a test, and the positive result, that confirms the presence of a

Question 2, shown as an image

Test

(2)

Answer
Mark scheme for question 2(a)(i)
(a)(ii)
Figure for question 2 Figure for question 2

(3)

Answer
Mark scheme for question 2(a)(ii)
(b)

Prop-2-en-1-ol can polymerise to form an addition polymer.

Write a balanced equation for this polymerisation.

(2)

Answer
Mark scheme for question 2(b)
(c)

Prop-2-en-1-ol can form the alkene propadiene, which has two adjacent

Question 2, shown as an image
Figure for question 2

propadiene

Explain why the CH2 groups at each end of the molecule are at right angles to each other. Use your knowledge of how orbitals overlap to form π-bonds.

(2)

Answer
Mark scheme for question 2(c)
(d)

The compound bombykol is a pheromone secreted by female silk moths. Like prop-2-en-1-ol, it can also be classified as both an alkene and an alcohol.

Figure for question 2

Bombykol can exist as a number of geometric isomers.

(d)(i)

Give the number of different geometric isomers of bombykol.

(1)

Answer
Mark scheme for question 2(d)(i)
(d)(ii)

Give the reason why prop-2-en-1-ol does not exhibit geometric isomerism.

(1)

Answer
Mark scheme for question 2(d)(ii)
(d)(iii)

Explain the expected solubilities in water of bombykol and prop-2-en-1-ol.

(3)

Answer
Mark scheme for question 2(d)(iii)

Question 3

A student carries out a series of qualitative tests to identify the contents of three unlabelled bottles. The bottles are known to contain the following solutions.

• ammonium carbonate, (NH4)2CO3(aq)

• potassium carbonate, K2CO3(aq)

• potassium sulfate, K2SO4(aq)

The student has access to just test tubes and a water bath, plus only the reagents shown.

AgNO3(aq) BaCl2(aq) Ca(OH)2(aq) CuSO4(aq)

HCl(aq) HNO3(aq) MgCl2(aq) NaOH(aq)

red litmus paper
blue litmus paper

The student carries out qualitative tests to positively identify either an anion or a cation in each compound and so identify the contents of each bottle.

Describe the qualitative tests carried out, the expected observations and appropriate deductions.

(6)

Answer
Mark scheme for question 3

Question 4

This question is about the kinetics of the reaction between iodine and propanone under acidic conditions. The equation for the reaction is shown.

Question 4, shown as an image

An experiment is carried out to determine the order of the reaction with respect to iodine.

Step 1 50.0 cm3 of 0.0200 mol dm−3 iodine solution, I2(aq), is added from a burette to a conical flask.

Step 2 25.0 cm3 of 2.00 mol dm−3 sulfuric acid, H2SO4(aq), is added to the conical flask using a pipette.

Step 3 25.0 cm3 of 2.00 mol dm−3 propanone solution, CH3COCH3(aq), is added to the conical flask using a pipette. The flask is swirled and a timer is started.

Step 4 After 2 minutes, a 10.0 cm3 sample of the reaction mixture is removed and quenched.

Step 5 The quenched sample is then titrated using 0.0100 mol dm−3 sodium thiosulfate solution, Na2S2O3(aq).

Step 6 Steps 4 and 5 are repeated every two minutes, until six titres have been determined.

(a)

Before carrying out Step 2, a student noticed droplets of an unknown colourless aqueous solution in the pipette.

Describe how the pipette should be treated before it is used in Step 2. Justify your answer.

(2)

Answer
Mark scheme for question 4(a)
(b)

Samples from the reaction mixture are quenched in Step 4.

(b)(i)

Explain why quenching is necessary.

(2)

Answer
Mark scheme for question 4(b)(i)
(b)(ii)

State a compound which can be added to the reaction mixture to quench the reaction. Include an equation for the reaction that takes place during the quenching process. State symbols are not required.

Compound

(2)

Answer
Mark scheme for question 4(b)(ii)
(c)
Figure for question 4 Figure for question 4

(2)

Answer
Mark scheme for question 4(c)
(d)

Show, by calculating the initial quantities of the reactants involved, that this experiment provides evidence for the order with respect to iodine only.

(4)

Answer
Mark scheme for question 4(d)
(e)

The results of the experiment are shown.

Time / minTitre / cm3
217.00
415.60
614.00
812.50
1011.00
129.40
(e)(i)

Plot a graph of titre against time.

(2)

Answer
Mark scheme for question 4(e)(i)
(e)(ii)

Give the reason why it is not necessary to calculate the concentration of iodine so that the order can be deduced.

(1)

Answer
Mark scheme for question 4(e)(ii)
(e)(iii)

Deduce the order with respect to iodine. Justify your answer.

(2)

Answer
Mark scheme for question 4(e)(iii)

Question 5

This question is about cobalt complexes.

(a)

A sample of cobalt(II) chloride was dissolved in aqueous ammonia, NH3(aq). During the process, a stream of oxygen was gently bubbled through the solution to oxidise the cobalt(II) ion.

A coloured solid, R, was extracted from the solution. A pure sample of this solid was found to contain the masses of the elements shown and had a molar mass of 233.4 g mol−1.

ElementMass / g
Co1.26
N1.20
H0.257
Cl2.28
(a)(i)

Show that the empirical formula and the molecular formula of R is CoN4H12Cl3. You must show your working.

(2)

Answer
Mark scheme for question 5(a)(i)
(a)(ii)

1.00 g of R was dissolved in water forming a coloured solution of the complex ion, Q.

The solution was reacted with excess silver nitrate solution, forming 0.614 g of silver chloride, AgC l (s).

Calculate the number of moles of chloride ions released when 1 mol of R dissolves.

(2)

Answer
Mark scheme for question 5(a)(ii)
(a)(iii)

Draw the three-dimensional shape of the complex ion, Q, using your answer to (a)(ii) to help deduce the formula and overall charge.

(3)

Answer
Mark scheme for question 5(a)(iii)
(b)

An aqueous solution of cobalt(II) chloride contains the complex ion [Co(H2O)6]2+.

The dynamic equilibria shown occur when NH3(aq) and EDTA4−(aq) are each added to separate solutions of this complex ion.

[Co(H2O)6]2+(aq) + 6NH3(aq) maths symbol [Co(NH3)6]2+(aq) + 6H2O(l) log Kc = 4.39

[Co(H2O)6]2+(aq) + EDTA4−(aq) maths symbol [Co(EDTA)]2−(aq) + 6H2O(l) log Kc = 16.5

(b)(i)

State what is meant by the term ‘dynamic equilibrium’.

(2)

Answer
Mark scheme for question 5(b)(i)
(b)(ii)

Explain, in terms of equilibria and entropy, which of the three complex ions is the most stable.

(3)

Answer
Mark scheme for question 5(b)(ii)

Question 6

The compound 2-methyl-1-phenylpropan-2-ol is found in small amounts in cocoa beans and has the structure shown.

Figure for question 6
(a)

A proposed synthesis of 2-methyl-1-phenylpropan-2-ol from phenylmethanol and propanone is shown.

Complete the diagram to show the structures of compounds A, B and C and the formula of reagent D.

Figure for question 6

(4)

Answer
Mark scheme for question 6(a)
(b)

2-Methyl-1-phenylpropan-2-ol can be converted to compound S. When considering the1H NMR spectrum of S, the hydrogen atoms of the benzene have been assumed to be a single environment, labelled J. The other hydrogen environments have been labelled K, L, M and N.

Figure for question 6

Complete the table for each of the environments K to N in the high resolution 1H NMR spectrum of S.

Figure for question 6

(5)

Answer
Mark scheme for question 6(b)

Question 7

A laboratory technician analysed a sample of an alcoholic drink to determine the concentration of ethanol, in g dm−3.

20.00 cm3 of the alcoholic drink was added to a 250 cm3 volumetric flask and made up to the mark with deionised water.

The ethanol in 5.00 cm3 of the diluted sample was oxidised in the equipment shown.

The sample was suspended in an open beaker in a sealed conical flask over 10.00 cm3 of acidified sodium dichromate(VI), of concentration 0.0780 mol dm−3.

Figure for question 7

The apparatus was left in a warm place for 24 hours for the acidified sodium dichromate(VI) to oxidise the ethanol.

Excess potassium iodide solution was then added to the remaining acidified sodium dichromate(VI) in the conical flask, forming iodine.

All of this iodine was then titrated using 0.0220 mol dm−3 sodium thiosulfate solution, Na2S2O3(aq).

The volume of Na2S2O3(aq) required in the titration was 32.70 cm3.

The equations for the reactions that take place during the experiment are shown.

Question 7, shown as an image
(a)

Explain why the apparatus was left in a warm room and for 24 hours.

(2)

Answer
Mark scheme for question 7(a)
(b)
(b)(i)

Calculate the number of moles of ethanol in 5 cm3 of the diluted drink.

(5)

Answer
Mark scheme for question 7(b)(i)
(b)(ii)

Calculate the concentration of ethanol in the alcoholic drink in g dm−3.

(3)

Answer
Mark scheme for question 7(b)(ii)
(c)

It was suggested that the titration as described might lead to an unreliable result.

State two ways the procedure could be amended to counter this suggestion.

(2)

Answer
Mark scheme for question 7(c)
(d)

Another technician suggested that it was unnecessary to suspend the drink sample above the acidified sodium dichromate(VI) solution and proposed a change to the procedure.

The proposal was that the drink sample should be mixed with the acidified sodium dichromate(VI) solution and then heated under reflux to allow the ethanol to be oxidised.

Give one reason to support this change and one reason to leave the method unchanged. In each case justify your answer.

Reason to support this change

Reason to leave the method unchanged

(2)

Answer
Mark scheme for question 7(d)

Question 8

This question is about weak acids.

(a)

An aqueous solution of a weak acid, HA(aq), with a concentration of 0.0712 mol dm−3, has a pH = 3.25 at room temperature.

Calculate the value of Ka for the weak acid HA(aq).

(2)

Answer
Mark scheme for question 8(a)
(b)

The value of Ka may be determined from experimental data, using a titration curve.

Ethanoic acid, CH3COOH(aq), with a concentration of 0.0500 mol dm−3, has a pH of 3.03 at room temperature.

A 20.0 cm3 sample of the acid was titrated with sodium hydroxide solution, NaOH(aq), with a concentration of 0.0500 mol dm−3. During the experiment, 40.0 cm3 of sodium hydroxide solution was slowly added to the ethanoic acid.

A pH probe connected to a data logger was used to monitor the pH throughout the experiment.

(b)(i)

Calculate the pH of the sodium hydroxide solution. Give your answer to one decimal place.

[Kw = 1.00maths symbol10−14mol2dm−6]

(1)

Answer
Mark scheme for question 8(b)(i)
(b)(ii)

Draw a titration curve, on the axes shown, to show the change in pH throughout the experiment.

Figure for question 8

(3)

Answer
Mark scheme for question 8(b)(ii)
(b)(iii)

Give an estimate of the pH value at the half-equivalence point. Show your working on the titration curve.

(1)

Answer
Mark scheme for question 8(b)(iii)
(b)(iv)

Calculate a value for Ka of ethanoic acid using your answer to (b)(iii). You must show your working.

(3)

Answer
Mark scheme for question 8(b)(iv)
(c)

Another method used to monitor the titration is to use a pH meter without a data logger. The pH is measured and recorded after the addition of each 1.00 cm3 portion of NaOH(aq).

A student assessed the two methods and concluded that using the data logger was a more effective way to carry out the experiment.

Give three reasons that support this conclusion.

(3)

Answer
Mark scheme for question 8(c)
(d)

A solution containing propanoic acid and sodium propanoate forms a buffer.

(d)(i)

2.30 g of sodium propanoate is dissolved in propanoic acid solution. This forms a buffer with pH = 4.2 and a volume of exactly 100 cm3.

Calculate the concentration of the propanoic acid, in mol dm–3, in this buffer.

[Ka (propanoic acid) = 1.34×10−5mol dm−3 Mr(CH3CH2CO2Na) = 96.0]

(4)

Answer
Mark scheme for question 8(d)(i)
(d)(ii)

Explain why there is no significant change in pH when a small amount of hydrochloric acid, HC l (aq), is added to this buffer.

(3)

Answer
Mark scheme for question 8(d)(ii)

Question 9

This question is about the compound 2,5-dimethylbenzenesulfonic acid, which has the structure shown.

Figure for question 9

It is used to analyse levels of cholesterol in blood plasma. It can be synthesised by the reaction of 1,4-dimethylbenzene with concentrated sulfuric acid. The electrophile in this reaction is sulfur trioxide.

(a)

Complete a possible mechanism for this reaction by adding curly arrows, and any relevant dipoles, charges and lone pairs.

Figure for question 9

(3)

Answer
Mark scheme for question 9(a)
(b)

The 2,5-dimethylbenzenesulfonic acid formed can be purified by recrystallisation using hot water as a solvent.

Procedure

Step 1 Dissolve impure 2,5-dimethylbenzenesulfonic acid in the minimum volume of hot water.

Step 2 Allow the solution to cool until 2,5-dimethylbenzenesulfonic acid has crystallised.

Step 3 Separate the 2,5-dimethylbenzenesulfonic acid by filtering under reduced pressure.

Step 4 Rinse the 2,5-dimethylbenzenesulfonic acid using a small amount of ice‑cold water.

Step 5 Dry the 2,5-dimethylbenzenesulfonic acid between two pieces of filter paper.

(b)(i)

Explain how recrystallisation reduces the amount of soluble impurities.

(3)

Answer
Mark scheme for question 9(b)(i)
(b)(ii)

A student carrying out this procedure noticed some insoluble impurities in their sample.

Describe how the procedure should be amended to remove these insoluble impurities.

(2)

Answer
Mark scheme for question 9(b)(ii)
(c)

The hydrated form of the acid has the formula C6H3(CH3)2SO3H•nH2O. An experiment was carried out to determine the number of moles of water of crystallisation, n, in this formula.

The method involves adding excess sodium hydroxide to a known mass of the hydrated 2,5-dimethylbenzenesulfonic acid. The amount of unreacted sodium hydroxide is then determined by titration.

Procedure

Step 1 10.0 cm3 of 1.00 mol dm−3 NaOH(aq) was added to 1.60 g of hydrated 2,5-dimethylbenzenesulfonic acid in a small conical flask.

Step 2 The solution formed was diluted to give a volume of exactly 100 cm3.

Step 3 20.0 cm3 samples of the diluted solution required a mean titre of 22.40 cm3 of 0.02500 mol dm−3 HCl(aq) to neutralise the unreacted sodium hydroxide present in the sample.

(c)(i)

Describe how to make the diluted solution, in Step 2.

(4)

Answer
Mark scheme for question 9(c)(i)
(c)(ii)

Calculate the relative formula mass of hydrated 2,5-dimethylbenzenesulfonic acid and hence deduce the value of n.

(5)

Answer
Mark scheme for question 9(c)(ii)
(d)

A student carrying out this experiment used a funnel as shown to try to ensure the acid was added safely to the burette during the titration.

Figure for question 9
(d)(i)

Give one change to this technique that would reduce the risk to this student.

(1)

Answer
Mark scheme for question 9(d)(i)
(d)(ii)

The student forgot to remove the funnel from the burette and during the titration five drops of acid from the funnel dripped into the burette.

Explain what effect, if any, this error will have on the final value for n.

(3)

Answer
Mark scheme for question 9(d)(ii)

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