A Level Chemistry 9701 Paper 21, May/June 2025

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9701/21 · May/June 2025

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1
a(i)

Solid sodium conducts electricity. Sodium oxide conducts electricity when molten but not when solid. Name the type of bonding present in sodium and in sodium oxide. bonding in sodium ............................................................................................................. bonding in sodium oxide ...................................................................................................

[1]
a(ii)

Explain how solid sodium conducts electricity.

[1]
a(iii)

Explain why sodium oxide conducts electricity when molten.

[1]
b(i)

Separate samples of sodium and sodium oxide are each added to an excess of cold water. Write an equation for the reaction of sodium with cold water.

[1]
b(ii)

Write an equation for the reaction of sodium oxide with cold water.

[1]
b(iii)

Complete Table 1.1. Do not refer to temperature changes when considering observations for these reactions. Table 1.1

sodiumsodium oxide
one similarity in observation on addition to cold water
one difference in observation on addition to cold water
[2]
c

State the oxidation number of the Period 3 elements bonded to Cl in NaCl and PCl5. Explain the difference in the oxidation number.

[2]
d

Table 1.2 shows melting points of some oxides. Table 1.2

oxidemelting point/ ∘C
SO2−73
H2O0
SO317
SiO21610
MgO2852
Al2O32072

A student suggests the following hypothesis. The higher the oxidation number of the element combined with oxygen, the higher the melting point of the oxide. Use Table 1.2 to deduce if this hypothesis is true or false or if there is not enough information to make a conclusion. Explain your answer.

[2]
2

A sample of iron is analysed using a mass spectrometer. The mass spectrum shows three isotopes of iron are present in the sample.

Figure 1 of 1 for question 2
a

Define isotopes.

[1]
b(i)

Fig. 2.1 shows the mass spectrum of the sample of iron. Use Fig. 2.1 to calculate the relative atomic mass, Ar, of iron to one decimal place. Show your working. Ar of iron=..............................

[2]
b(ii)

Complete Table 2.1 to show the number of protons and nucleons in one atom of 56Fe. Table 2.1

particlenumber of particles in one atom of 56Fe
protons
nucleons
[2]
c

Deduce the number of pairs of electrons in the shell with principal quantum number n=3 in an Fe atom. number of pairs of electrons ..............................

[1]
d

Write an equation to represent the first ionisation energy of iron.

[1]
e

Suggest how the value for the first ionisation energy of 54Fe compares to the first ionisation energy of 56Fe. Explain your answer in terms of the factors that affect ionisation energy.

[4]
3
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Figure 5 of 5 for question 3
a(i)

Hexene reacts with hydrogen gas to produce hexane. reaction 1C6H12(l)+H2(g)→C6H14(l) Fig. 3.1 shows the distribution of energies of H2(g) molecules at temperature T. Sketch on Fig. 3.1 the shape of the curve for the same sample of H2(g) molecules when the temperature is increased.

[2]
a(ii)

Explain why increasing the temperature increases the rate of reaction 1.

[2]
a(iii)

State the role of nickel when it is added to reaction 1.

[1]
a(iv)

Annotate Fig. 3.2 to show the effect of adding nickel to reaction 1 at temperature T.

[1]
b

Define Le Chatelier’s principle.

[2]
c

Reaction 2 shows the equilibrium reaction between X(g) and Y(g) to produce Z(g) in a sealed container. reaction 2aX(g)+bY(g)⇌cZ(g) Fig. 3.3 shows the effect of changing pressure on the percentage yield of Z(g) at two different temperatures, 300 K and 350 K. Deduce two conclusions about reaction 2 using Fig 3.3.

[2]
4

The structure of vitamin C is shown in Fig. 4.1.

Figure 1 of 5 for question 4
Figure 2 of 5 for question 4
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Figure 5 of 5 for question 4
a

Deduce the empirical formula of vitamin C.

[1]
b(i)

The concentration of vitamin C is found by titration with I2(aq). A vitamin C tablet is dissolved in water to produce 200.0 cm3 of vitamin C solution. 5.00 cm3 of this vitamin C solution is added to a flask with approximately 150 cm3 of water and an indicator. Exactly 28.40 cm3 of 5.00×10−4 mol dm−3 I2(aq) reacts with the sample of vitamin C solution in the flask. [Mr: vitamin C, 176] Calculate the amount, in mol, of I2(aq) added to the flask in this titration. amount of I2(aq)=..............................mol

[1]
b(ii)

Use your answer to (b)(i) to calculate the mass, in g, of vitamin C in the tablet. Show your working. (If you were unable to calculate a value for the amount of I2(aq) in (b)(i), use the value 2.64×10−4 mol. This is not the correct value.) mass of vitamin C in tablet=..............................g

[2]
b(iii)

Deduce the role of I2(aq) in the reaction in Fig. 4.2.

[1]
b(iv)

Suggest two reasons why hot concentrated acidified potassium manganate(VII) is not a suitable reagent for producing Q from vitamin C. 1 ........................................................................................................................................ ........................................................................................................................................... 2 ........................................................................................................................................ ...........................................................................................................................................

[2]
c

Predict two absorptions that will be seen in the infrared spectra of both vitamin C and Q. Describe the relevant bond and the specific functional group that is responsible for each absorption identified.

[2]
5

Compound A contains the elements carbon, hydrogen and oxygen only. When A is heated with H2SO4(aq), compounds B and C are produced, as shown in Fig. 5.1. A+2H2O→heatH2SO4(aq)HOOCCH2COOHB+2CH3CH2OHC

Figure 1 of 1 for question 5
a

Draw the structure of A.

[2]
b

Name the type of reaction that occurs when A is heated with H2SO4(aq).

[1]
c(i)

When aqueous Na2CO3 is added to separate samples of B and C, effervescence is observed with B only. Complete the equation to describe the reaction between B and an excess of aqueous Na2CO3. ......HOOCCH2COOH + ......Na2CO3→ .............................................................................

[1]
c(ii)

Suggest why C does not react with aqueous Na2CO3 in a similar type of reaction to B.

[1]
d(i)

A student suggests a two-step synthesis to produce B, as shown in Fig. 5.2. Identify the reagents and conditions required in steps 1 and 2. step 1 ................................................................................................................ step 2 ................................................................................................................

[2]
d(ii)

Identify the type of reaction that HOCH2CH2CH2OH undergoes in step 2.

[1]
e(i)

B reacts with an excess of reducing agent R to produce D. An excess of PCl5 is added to D. • A vigorous reaction occurs. • Misty fumes are seen. • Organic compound E is produced. Identify the formula of the reducing agent R.

[1]
e(ii)

Complete the equation to describe the reaction of B with an excess of R. Use [H] to represent one atom of hydrogen from R. ......HOOCCH2COOH + ......[H]→ ...............................................................................

[2]
e(iii)

Name organic compound E.

[1]
6

Three bottles of colourless liquids labelled F, G and H contain separate pure samples of the compounds ethanal, propanal or propanone but not necessarily in that order.

a

State the functional group in ethanal, propanal and propanone.

[1]
b

State a reagent and the relevant observation that confirm that F, G and H have the same functional group. reagent ..................................................................................................................................... observation ...............................................................................................................................

[2]
c(i)

Separate samples of F, G and H are each tested with Tollens’ reagent and with alkaline I2(aq). The observations are shown in Table 6.1. Table 6.1

Tollens’ reagentalkaline I2(aq)
Fno observable changepale yellow precipitate
Gsilver mirrorpale yellow precipitate
Hsilver mirrorno precipitate

Use Table 6.1 to name the organic compounds in bottles F, G and H. F = ............................................. G = ............................................. H = .............................................

[2]
c(ii)

Identify the yellow precipitate produced when alkaline I2(aq) is added to separate samples of F and G.

[1]
c(iii)

Compound J does not contain the same functional group as F, G and H. Compound J also reacts with alkaline I2(aq) to produce a pale yellow precipitate. Suggest the structure of compound J.

[1]

Mark scheme

9701/21 · May/June 2025

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1a(i) · 1 mark

  • 1 mark

    sodium – metallic AND sodium oxide – ionic

1a(ii) · 1 mark

  • 1 mark

    delocalised electrons move (through the structure)

1a(iii) · 1 mark

  • 1 mark

    (sodium and oxide) ions move (through the liquid)

1b(i) · 1 mark

  • 1 mark

    2Na + 2H2O → 2NaOH + H2

1b(ii) · 1 mark

  • 1 mark

    Na2O + H2O → 2NaOH

1b(iii) · 2 marks

  • 1 mark

    one similarity: (both) solids disappear OR (both produce) colourless solutions

  • 1 mark

    one difference: effervescence AND no effervescence

1c · 2 marks

  • M1

    NaCl +1 AND PCl 5 + 5

  • M2

    Na has only 1 valence (shell) electrons AND P has 5

1d · 2 marks

  • 2 marks

    All three for two marks: - false - comparison or statement of oxidation number - correct link to melting point from their comparison or statement

2a · 1 mark

  • 1 mark

    atoms (of an element) with same number of protons and different number of neutrons

2b(i) · 2 marks

  • M1

    method showing each abundance multiplied by m/e value: (5.9  54) and (91.9  56) and (2.2  57) OR (0.59  54) and (9.19  56) and (0.22  57)

  • M2

    the three values from M1 expressed as a percentage and added together correctly with final answer to 1 d.p: 5.9/100  54 + 91.9/100  56 + 2.2/100  57 = 55.9

2b(ii) · 2 marks

  • 1 mark

    protons: 26

  • 1 mark

    nucleons: 56

2c · 1 mark

  • 1 mark

    5

2d · 1 mark

  • 1 mark

    Fe(g) → Fe+(g) + e(-)

2e · 4 marks

  • M1

    same electronic configuration OR same shielding

  • M2

    same number of protons OR same nuclear charge

  • M3

    so same nuclear attraction to outer shell electron

  • M4

    no change / will not be affected

3a(i) · 2 marks

  • 1 mark

    start at origin

  • 1 mark

    peak sits below the original, peak sits to the right-hand side of the original, new line crosses the original once only AND to the right of the original peak

3a(ii) · 2 marks

  • M1

    greater proportion of (H2) molecules have energy greater than or equal to the activation energy /  EA

  • M2

    increase in frequency of successful collisions (between H2 and C6H12)

3a(iii) · 1 mark

  • 1 mark

    catalyst

3a(iv) · 1 mark

  • 1 mark

    annotation to show new EA (nickel / catalyst) further to the left than original EA

3b · 2 marks

  • M1

    (if a change is made at a system is dynamic equilibrium) the equilibrium moves

  • M2

    to minimise the change in conditions

3c · 2 marks

  • 1 mark

    (forward) reaction is exothermic

  • 1 mark

    (a + b)  c

4a · 1 mark

  • 1 mark

    C3H4O3

4b(i) · 1 mark

  • 1 mark

    (28.40 / 1000  0.0005) = 1.42  10-5 mol

4b(ii) · 2 marks

  • M1

    correct method to deduce mass of vit C in 5 cm3 sample (1.42  10–5  176) = 2.49  10–3 OR correct method to deduce amount, mol, vit C in 5 cm3 sample (1.42  10–5  200 / 5) = 5.68  10–4

  • M2

    correct calculation for mass of vit C in original solution (2.49  10–3  200 / 5) = 0.099968 OR correct calculation for mass of vit C in original solution = M1  176 [(5.68 10–4)  176 = 0.099968]

4b(iii) · 1 mark

  • 1 mark

    oxidising agent

4b(iv) · 2 marks

  • M1

    (also) oxidises / reacts with (primary and / or secondary) alcohol groups

  • M2

    (also) breaks the sigma and pi bond in C=C

4c · 2 marks

  • 1 mark

    1040 – 1300, C–O, ester / hydroxy

  • 1 mark

    3200 – 3650, O–H, hydroxy / alcohols

  • 1 mark

    2850 – 2950, C–H, alkane

  • 1 mark

    1710 – 1750, C=O, ester

5a · 2 marks

  • M1

    two ester links

  • M2

    rest of structure correct

5b · 1 mark

  • 1 mark

    (acid) hydrolysis

5c(i) · 1 mark

  • 1 mark

    HOOCCH2COOH + Na2CO3 → NaOOCCH2COONa +CO2 + H2O

5c(ii) · 1 mark

  • 1 mark

    C is not as strong an acid as B

5d(i) · 2 marks

  • M1

    NaOH(aq) AND heat

  • M2

    acidified AND potassium dichromate(VI) AND heat under reflux

5d(ii) · 1 mark

  • 1 mark

    oxidation

5e(i) · 1 mark

  • 1 mark

    LiAlH4

5e(ii) · 2 marks

  • M1

    correct unambiguous organic product

  • M2

    correct balanced equation: HOOCCH2COOH + 8[H] → HOCH2CH2CH2OH + 2H2O

5e(iii) · 1 mark

  • 1 mark

    1,3-dichloropropane

6a · 1 mark

  • 1 mark

    carbonyl

6b · 2 marks

  • M1

    (2,4)-dinitrophenylhydrazine / (2,4)-DNPH

  • M2

    orange / red / yellow precipitate

6c(i) · 2 marks

  • 2 marks

    F = propanone G = ethanal H = propanal

6c(ii) · 1 mark

  • 1 mark

    tri-iodomethane OR CHI3

6c(iii) · 1 mark

  • 1 mark

    CH3CH(OH)-R where R is represented as H or any alkyl group

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