Mass spectra and IR: Edexcel International A Level Chemistry questions
Every Edexcel International A Level Chemistry exam question on 10D Mass spectra and IR (specification points 10.21–10.23), 2019–2025, with its mark scheme and examiner’s report.
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Calculations
Q12(a)
The whole paper ↗Your answerQ16(c)(ii)
The whole paper ↗Q1(c)
The whole paper ↗Q1(d)
The whole paper ↗Q20(c)
The whole paper ↗Q18(c)
The whole paper ↗Q14(b)
The whole paper ↗Your answer- Your answer
Q20(a)(ii)
The whole paper ↗Q20(a)(iii)
The whole paper ↗Q20(b)(ii)
The whole paper ↗Q20(b)(iii)
The whole paper ↗- Your answer
Q23(c)(iii)
The whole paper ↗Q1(c)(i)
The whole paper ↗Q1(c)(ii)
The whole paper ↗Q15(a)
The whole paper ↗Your answerQ15(b)
The whole paper ↗Your answerQ4(f)
The whole paper ↗
All 63 questions on Mass spectra and IR, as a list
- June 2025, AS Unit 2, Q12(a) (1 mark): Which compound has peaks in its mass spectrum at m/z 74 and 45? (1) A butanone B butanal C butan-2-ol D methylpropan-2-ol
- June 2025, AS Unit 2, Q16(c)(ii) (2 marks): The infrared spectrum of cyclohexanol is shown. Transmittance 3000 2000 1000 Wavenumber / cm–1 Describe two differences, other than the fingerprint region, that
- June 2025, AS Unit 3, Q1(c) (3 marks): Mass spectra of P and Q show a molecular ion peak at m / z = 60. The mass spectrum of P has its most intense peak at m / z = 31 and this peak is not present in
- June 2025, AS Unit 3, Q1(d) (2 marks): Deduce the structural formulae of P and Q. (2) P Q
- June 2025, Unit 5, Q20(c) (2 marks): The infrared spectrum for salicylic acid is shown. 100 Transmittance / % 50 0 4000 3000 2000 1500 1000 500 Wavenumber / cm–1 Identify two wavenumbers on the spe
- June 2025 (A), Unit 5, Q18(c) (3 marks): There are two possible products in Step 4. Describe how these could be distinguished using infrared spectroscopy. Refer to three different types of bond and the
- January 2025, AS Unit 2, Q20 (6 marks): *20 A bottle has lost its label. The content of the bottle is thought to be one of 1-hydroxypropanone, propenoic acid or butan-1-ol. O O OH OH OH 1-hydroxypropa
- October 2024, AS Unit 2, Q14(b) (1 mark): Which compound could give peaks at m / z = 31 and m / z = 60 in its mass spectrum? (1) A propan-1-ol B propan-2-ol C propanal D propanone Use this space for any
- October 2024, AS Unit 2, Q15 (1 mark): An infrared spectrum for a compound containing one functional group is shown. 100 Transmittance / % 50 0 4000 3000 2000 1500 1000 500 Wavenumber / cm–1 Which fu
- June 2024, AS Unit 2, Q20(a)(ii) (2 marks): The peaks with the highest intensity in the mass spectrum of isoprene are at m / z = 68 and m / z = 53. Identify the species responsible for these two peaks. (2
- June 2024, AS Unit 2, Q20(a)(iii) (3 marks): The infrared spectrum of isoprene is shown. R P Transmittance Q / % 3000 2000 1000 Wavenumber / cm–1 State the origins of the peaks labelled P, Q and R. You may
- June 2024 (R), AS Unit 2, Q20(b)(ii) (3 marks): Acetoin also contains the carbonyl group C an aldehyde. Use page 5 of your Data Booklet to show how infrared spectra data could be used to prove that acetoin co
- June 2024 (R), AS Unit 2, Q20(b)(iii) (3 marks): Part of the mass spectrum of acetoin is shown. 100 80 60 Relative intensity 40 20 0.0 15 30 45 60 75 90 m / z Determine a possible structure of acetoin using yo
- January 2024, AS Unit 2, Q20 (1 mark): Which compound gives this mass spectrum? 100 80 60 Relative intensity 40 20 0 10 15 20 25 30 35 40 45 50 55 60 m / z A CH3COOH B CH3COCH3 C CH3CH2CHO D CH3CH2CH
- January 2024, AS Unit 2, Q23(c)(iii) (2 marks): Give the wavenumber range of an absorption in the infrared spectrum of the organic product of reaction R4, which is not present in the infrared spectrum of CH3C
- January 2024, AS Unit 3, Q1(c)(i) (1 mark): Deduce the m/z ratio of the fragment shown by the unshaded area, assuming it forms a singly charged ion. (1)
- January 2024, AS Unit 3, Q1(c)(ii) (1 mark): When molecular ions fragment, they form a smaller ion and another type of particle. State the other type of particle formed. (1)
- January 2024, Unit 4, Q15(a) (1 mark): The mass spectrum of compound X shows a large peak at m/z = 59. This peak is due to the fragmentation of the molecular ion. Which compound is most likely to be
- January 2024, Unit 4, Q15(b) (1 mark): Compound Y does not react with acidified aqueous sodium dichromate. The infrared spectrum of Y is shown. 100 % Transmittance 0 3000 2000 1000 Wavenumber / cm–1
- January 2024, Unit 6, Q4(f) (3 marks): An infrared spectrum of phenylethanamide and an infrared spectrum of phenylamine were obtained. One of these two spectra is shown with two peaks circled. 100 Tr
- October 2023, AS Unit 2, Q14(a) (1 mark): When propan‑2‑ol is refluxed with excess acidified potassium dichromate(VI), the product will show a peak due to (1) A O H stretching at 3750 – 3200 cm–1 B C O
- October 2023, AS Unit 2, Q14(b) (1 mark): When propan‑1‑ol is heated with acidified potassium dichromate(VI), the product that is distilled off as it is formed will show a peak due to (1) A O H stretchi
- October 2023, AS Unit 2, Q21(a)(ii) (2 marks): The mass spectrum of X is shown. 100 80 60 Percentage relative 40 abundance 20 0.0 30 40 50 60 70 80 90 m / z Deduce the molecular formula of X, using the mass
- October 2023, AS Unit 2, Q21(a)(iv) (2 marks): Using your answer to (a)(iii) and the mass spectrum, complete Table 2. (2) Table 2 Peak in mass spectrum Formula of ion m / z = 41 m / z = 45
- June 2023, AS Unit 2, Q21(c) (2 marks): Explain how the infrared spectra of methanol and methanal can be used to distinguish between the two compounds, stating the relevant bond stretching vibrations
- June 2023, AS Unit 3, Q2(d)(ii) (1 mark): Some infrared data are given in the table. Group Wavenumber range / cm–1 O H stretching in alcohols 3750–3200 O H stretching in carboxylic acids 3300–2500 C O s
- June 2023, AS Unit 3, Q2(d)(iii) (2 marks): A student suggested that the structure of D could be identified using mass spectrometry because only one of the possible structures of D would have a peak at m
- June 2023, Unit 6, Q2(c)(i) (1 mark): Bubbles are observed when aqueous sodium hydrogencarbonate is added to Y. Deduce the formula of the ion responsible for the peak at m / z = 45. (1)
- January 2023, AS Unit 2, Q15 (1 mark): Which compound is least likely to have a prominent peak at m / z = 43 in its mass spectrum? A CH3COCH2CH3 B CH3CH2NHCH3 C CH3CH(CH3)2 D CH3CH2CH2CH3
- January 2023, AS Unit 2, Q16 (1 mark): Which compound has peaks at 3415 cm–1 and 2250 cm–1 in its infrared spectrum? Refer to the Data Booklet. A H2NCH2CH2C N B CH3CH2CH2COOH C ClCH2CH2C CH D HOCH2CH
- January 2023, Unit 5, Q11(a) (1 mark): Which of these wavenumber ranges would you not expect to have an absorption in the infrared spectrum of valine? (1) A 3500 – 3300 cm–1 B 3095 – 3010 cm–1 C 2962
- October 2022, AS Unit 2, Q22(c)(iii) (2 marks): Infrared spectroscopy provides information on functional groups. In an experiment, a sample of 2-methylpropan-1-ol was treated with an oxidising agent. Show tha
- June 2022, AS Unit 2, Q14(c) (1 mark): Cyclohexanol and cyclohexene each has a peak in their infrared spectrum which is not present for the other compound. Which are these peaks? (1) Peak only in cyc
- January 2022, AS Unit 2, Q24(d)(i) (1 mark): Draw a circle around an absorption in the spectrum that could be due to the stretching of the N H bond. (1)
- January 2022, AS Unit 2, Q24(d)(ii) (1 mark): Identify the bond responsible for the absorption at 1683 cm−1. . (1)
- January 2022, AS Unit 3, Q2(d) (2 marks): The infrared spectrum of Y is shown. 0.8 0.6 Transmittance 0.4 0.2 4000 3000 2000 1000 Wavenumber / cm–1 The table shows some infrared absorption data. Wavenumb
- January 2022, AS Unit 3, Q2(e)(i) (1 mark): Show that the mass spectrum is consistent with Y having the molecular formula C3H4O3 . (1)
- January 2022, AS Unit 3, Q2(e)(ii) (1 mark): Suggest the structure of the ion causing the peak at m / z = 43 in the mass spectrum of Y. (1)
- January 2022, Unit 5, Q5 (1 mark): The infrared spectrum of a compound X is shown. 100 90 80 70 60 % Transmittance 50 40 30 20 4000 3500 3000 2500 2000 1500 1000 500 Wavenumber / cm−1 Which could
- October 2021, AS Unit 2, Q1 (1 mark): The infrared spectrum of an organic compound is shown. 100 50 0 4000 3000 2000 1500 1000 500 Wavenumber / cm–1 Which of these compounds would give this infrared
- October 2021, AS Unit 2, Q4 (1 mark): In a mass spectrum, the molecular ion is the ion which always has the A greatest abundance B greatest stability C highest charge D highest mass/charge ratio
- October 2021, AS Unit 2, Q5 (1 mark): Butan-1-ol and butan-2-ol are isomers. Which m / z value would be expected to have a significant peak in the mass spectrum of butan-1-ol but not that of butan-2
- October 2021, Unit 6, Q2(b)(i) (1 mark): Give the formula of one of the ions responsible for the peak at m / z = 29. (1)
- 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
- June 2021, AS Unit 2, Q12 (1 mark): Which could be the infrared spectrum of CH2=CHCH2OH? 100 A % Transmittance 50 0 4000 3000 2000 1500 1000 500 Wavenumber / cm–1 100 % Transmittance 50 B 0 4000 3
- June 2021, AS Unit 2, Q13 (1 mark): The mass spectrum of propanone is shown. 100 80 60 Relative intensity 40 20 0 10 15 20 25 30 35 40 45 50 55 60 m / z Which fragment is most likely to produce th
- June 2021, AS Unit 2, Q22(d) (2 marks): Use your Data Booklet to suggest the wavenumber of a strong absorbance you would expect to see in the infrared spectrum for phosgene. Justify your answer. (2)
- June 2021, AS Unit 3, Q2(d)(i) (1 mark): Identify the wavenumber range and the bond responsible for one peak which you would expect to see in the infrared spectra of all three compounds. (1)
- June 2021, AS Unit 3, Q2(d)(ii) (1 mark): Identify the wavenumber range and the bond responsible for one peak which you would expect to see in the infrared spectra of only one of the compounds. (1)
- June 2021, AS Unit 3, Q2(d)(iii) (1 mark): Give a reason why there is a peak at m / z = 100 in the mass spectra of all three compounds. (1)
- June 2021, AS Unit 3, Q2(d)(iv) (2 marks): Fragmentation of 1-methylcyclopentanol results in a significant peak at m / z = 85. Suggest the structures of the two species formed when one bond in 1-methylcy
- June 2021, Unit 5, Q14 (1 mark): An aliphatic organic compound has the infrared spectrum shown. 100 P 50 Q 0 4000 3000 2000 1500 1000 500 Wavenumber / cm –1 What are the bond stretches responsi
- June 2021, Unit 6, Q3(d)(iii) (1 mark): The mass spectrum of the compound is shown. 100 80 60 Relative intensity 40 20 0 0 10 20 30 40 50 60 70 80 90 m / z Deduce the relative molecular mass of the co
- June 2021, Unit 6, Q3(d)(v) (2 marks): Determine the identity of the compound, using your answer to (d)(iv) and the fragmentation pattern of the mass spectrum. Justify your answer. (2) O O OH OH O B
- January 2021, Unit 4, Q17(d)(iii) (1 mark): The infrared spectrum of E has an absorption in the range 1750 – 1735 cm−1. Name the functional group in E. (1)
- October 2020, AS Unit 2, Q17(b)(iv) (3 marks): The infrared spectra of methanol and methanoic acid are shown. Explain how these could be used to show that all the methanol has been converted to methanoic aci
- October 2020, AS Unit 3, Q3(a)(v) (1 mark): State whether or not it is possible to distinguish between F and G using infrared spectra. Justify your answer. Wavenumber values are not required. (1)
- October 2020, Unit 6, Q2(a) (4 marks): Compound P is a colourless liquid with a sweet fruity smell. When a sample of P was heated with sodium hydroxide, a volatile product was formed which had a mole
- January 2020, AS Unit 2, Q14(a) (1 mark): Which m / z peak would not be expected in the mass spectrum of propanone? (1) A 15 B 29 C 43 D 58
- January 2020, AS Unit 2, Q17(d)(iii) (1 mark): Give the bond and the wavenumber range of its absorption in the infrared spectrum of 2-methylbutan-2-ol which would not be in the infrared spectrum of this chlo
- June 2019, AS Unit 2, Q18 (1 mark): Which of these carboxylic acids would be expected to have a major peak at m / z = 57 in its mass spectrum? A CH3CH2CH2COOH B CH3COOH C (CH3)2CHCOOH D CH3CH2COOH
- June 2019, AS Unit 2, Q22(b)(ii) (2 marks): Describe, by referring to wavenumbers and bonds, how the infrared spectra of the isomers differ from the infrared spectrum of alcohol Y. (2)
- June 2019, AS Unit 3, Q2(d)(ii) (3 marks): The mass spectrum of C4H8Br2 had a pair of peaks at m / z = 107 and m / z = 109 and also peaks at m / z = 79 and m / z = 81 due to the isotopes of bromine. One
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