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Deducing formulae and structures from data: Edexcel International A Level Chemistry questions

Edexcel International A Level Chemistry past-paper questions on 20.1.1 Deducing formulae and structures from data, 2019–2025, with mark schemes and examiner’s reports where available.

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  1. The start of question 19

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  2. Q23(a)

    January 2025 · Unit 5

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    The start of question 23

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  3. The start of question 3

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  4. Q3(c)

    January 2025 · Unit 6

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  5. Q1(c)(i)

    June 2024 · Unit 6

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  6. Q18(b)(v)

    January 2023 · Unit 4

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    The start of question 18

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  7. Q17(a)

    January 2023 · Unit 5

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    The start of question 17

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  8. The start of question 17

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  9. Q17(c)

    January 2023 · Unit 5

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  10. The start of question 17

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  11. The start of question 17

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  12. Q21(a)(ii)

    October 2022 · Unit 5

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  13. The start of question 14

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  14. Q14(b)

    June 2022 · Unit 5

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  15. The start of question 2

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  16. The start of question 20

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  17. The start of question 20

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  18. Q20(b)(iii)

    January 2022 · Unit 4

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  19. Q15(a)

    January 2022 · Unit 5

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  20. Q15(b)

    January 2022 · Unit 5

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All 35 questions on Deducing formulae and structures from data, as a list
  1. June 2025 (A), Unit 5, Q19(b)(ii) (3 marks): Determine the molecular formula of E, using the data shown and the information in (b). (3) % carbon % hydrogen % nitrogen % oxygen 51.1 8.51 15.1
  2. January 2025, Unit 5, Q23(a) (1 mark): Deduce the molecular formula of procaine. (1)
  3. January 2025, Unit 6, Q3(a) (4 marks): Qualitative tests on X show that it • burns in air with a very smoky flame • forms an orange precipitate with 2,4-dinitrophenylhydrazine (Brady’s reagent) does
  4. January 2025, Unit 6, Q3(c) (1 mark): The molecular formula of X is the same as its empirical formula. Use this information, and your answers to (a) and (b), to deduce the structure of X. (1)
  5. June 2024, Unit 6, Q1(c)(i) (2 marks): Draw the displayed formula of the two structural isomers of A, using this information and your answers from (a) and (b). (2)
  6. January 2023, Unit 4, Q18(b)(v) (1 mark): Draw the structure of X using the information from (b)(ii) to (b)(iv). (1)
  7. January 2023, Unit 5, Q17(a) (4 marks): An organic compound A contains carbon, hydrogen and oxygen only and has a molar mass of 136 g mol–1. Complete combustion of 5.26 g of A in dry oxygen produces 1
  8. January 2023, Unit 5, Q17(b) (5 marks): Compound A, C9H12O, contains a benzene ring and one side-chain. A is oxidised when heated with acidified potassium dichromate(VI) to produce a compound B which
  9. January 2023, Unit 5, Q17(c) (2 marks): Compound F is a structural isomer of A which also has a benzene ring and one side-chain. F is not oxidised when heated with acidified potassium dichromate(VI).
  10. January 2023, Unit 5, Q17(d) (2 marks): Compound G is a structural isomer of A which also has a benzene ring and one side-chain. The mass spectrum of G has a peak at m / z = 107. Deduce the structure
  11. October 2022, Unit 4, Q17(d) (6 marks): Sodium ethanoate, CH3COONa , reacts with 2-methylpropanoyl chloride, (CH3)2CHCOCl , to form organic compound Z and sodium chloride, NaCl . The molecular ion pea
  12. October 2022, Unit 5, Q21(a)(ii) (2 marks): Deduce the molecular formula of the alkyl group R, using the structure of coniine and its molar mass. You must show your working. (2)
  13. June 2022, Unit 5, Q14(a) (4 marks): Complete combustion of 6.02 g of Q produces 18.07 g of carbon dioxide and 3.30 g of water. Determine the empirical formula of Q. (4)
  14. June 2022, Unit 5, Q14(b) (6 marks): Tests on samples of Q show that it • burns in air with a very sooty flame • forms an orange precipitate with Brady’s reagent (2,4-dinitrophenylhydrazine solutio
  15. June 2022, Unit 6, Q2(c) (2 marks): The high resolution proton NMR spectrum of E is shown. P Q 11 10 9 8 7 6 5 4 3 2 1 0 δ / ppm The relative numbers of protons responsible for the singlet peaks s
  16. January 2022, Unit 4, Q20(b)(i) (3 marks): Compound A is thought to be another isomer of hexanoic acid. 10 g of compound A is found to contain 6.21 g of carbon and 1.03 g of hydrogen, with the remainder
  17. January 2022, Unit 4, Q20(b)(ii) (1 mark): State how you might use your answer to (b)(i) and a mass spectrum of compound A to prove that compound A is an isomer of hexanoic acid. (1)
  18. January 2022, Unit 4, Q20(b)(iii) (6 marks): A series of tests was performed on compound A. Test Observation 1 addition of phosphorus(V) chloride misty fumes 2 addition of 2,4‑dinitrophenylhydrazine orange
  19. January 2022, Unit 5, Q15(a) (4 marks): Combustion analysis of 4.91 g of Q produces 14.6 g of carbon dioxide and 3.58 g of water. Show that the molecular formula of Q is C10H12O . You must show all yo
  20. January 2022, Unit 5, Q15(b) (7 marks): The high resolution proton NMR spectrum of Q is shown. Area under curve 5 2 2 3 10 9 8 7 6 5 4 3 2 1 0 δ (ppm) Deduce the structure of Q. Justify your answer by
  21. January 2022, Unit 6, Q2(e)(i) (2 marks): Z has a fruity smell. Deduce the identity of the functional group present in Z, using all the information given. Include any relevant wavenumber ranges in your
  22. October 2021, Unit 4, Q16(a)(i) (1 mark): Give a reason why the oxygen used must be dry. (1)
  23. October 2021, Unit 4, Q16(a)(ii) (5 marks): Show that the empirical formula of X is C4H6O3 . You must show your working. (5)
  24. October 2021, Unit 4, Q16(b)(i) (6 marks): Deduce the two possible structures of X, showing how this information supports your answer. (6)
  25. October 2021, Unit 6, Q2(b)(ii) (1 mark): A contains one functional group. Give the m / z value of the molecular ion and the structure of A. (1) m / z value of the molecular ion structure of A
  26. October 2021, Unit 6, Q2(c)(ii) (1 mark): B has a molar mass of 59 g mol−1. Suggest a structure for B. (1)
  27. October 2021, Unit 6, Q4(f)(i) (1 mark): Deduce the formula of the alkyl group, R. (1)
  28. June 2021, Unit 5, Q19(c) (6 marks): A simplified high resolution proton NMR spectrum of Y is shown. The relative peak areas are given near each peak. 9 3 TMS 1 12.0 10.0 8.0 6.0 4.0 2.0 0.0 Chemic
  29. June 2021, Unit 5, Q19(d) (1 mark): Draw the structure of compound X. (1)
  30. June 2021, Unit 6, Q3(d)(i) (2 marks): Identify, by name or formula, suitable substances for solids M and N. (2) Solid M Solid N
  31. June 2021, Unit 6, Q3(d)(ii) (4 marks): Calculate the empirical formula of the compound, using the data given. You must show your working. (4)
  32. June 2021, Unit 6, Q3(d)(iv) (1 mark): Deduce the molecular formula of the compound, using your answers to (ii) and (d)(iii). (1)
  33. January 2021, Unit 5, Q17 (1 mark): When a sample of a hydrocarbon is burned completely in oxygen, 2.64 g of carbon dioxide and 0.81 g of water are formed. Which of these could be the molecular fo
  34. January 2021, Unit 5, Q22(a) (3 marks): Determine the molecular formula of CxHy . You must show your working. (3)
  35. October 2020, Unit 5, Q25(e)(ii) (4 marks): The Lanthanides The lanthanides form a series in the Periodic Table comprising the elements from lanthanum, La (Z = 57) to lutetium, Lu (Z = 71). They have impo

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