Forces between molecules: AQA A‑Level Chemistry questions
AQA A-Level Chemistry past-paper questions on 3.1.3.7 Forces between molecules, 2008–2025, with mark schemes and examiner’s reports where available.
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Q05.1
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Q02.3
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Q03.4
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Q07.3
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Q05.3
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Q06.3
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Q06.4
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Q04.1
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Q04.5
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Q05.1
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Q03.4
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Q04.1
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All 101 questions on Forces between molecules, as a list
- June 2025, Paper 1, Q05.1 (2 marks): Explain why chlorine has a lower boiling point than bromine. [2 marks]
- June 2025, AS Paper 2, Q02.3 (3 marks): Hydrogen bonds exist between molecules of liquid methanol. Draw a diagram to show a hydrogen bond between two molecules of methanol. Include all the lone pairs
- June 2025, AS Paper 2, Q03 (6 marks): Molecules of CCl4 and CHCl3 have similar tetrahedral shapes. The boiling point of CCl4 is 77 °C The boiling point of CHCl3 is 61 °C Explain why CCl4 has a highe
- June 2024, Paper 3, Q13 (1 mark): Which compound forms the greatest number of hydrogen bonds per molecule in the liquid state? [1 mark] A CH3CH2COOH B CH3CH2OCH3 C CH3CH2CHO D CH3CH2CH2OH
- June 2024, AS Paper 1, Q03.4 (3 marks): There are van der Waals forces between non-polar molecules. Explain what causes these forces. [3 marks]
- June 2024, AS Paper 2, Q07.3 (3 marks): Propanoic acid molecules cannot be separated from the reaction mixture by simple distillation because propanoic acid forms hydrogen bonds with water molecules.
- June 2024, AS Paper 2, Q17 (1 mark): Which of these alkanes has the highest boiling point? [1 mark] A decane B hexane C 2,3-dimethyloctane D 2,3-dimethylbutane
- June 2023, Paper 3, Q05.3 (3 marks): Explain the trend in the boiling points of the three compounds. Refer to the intermolecular forces in all three compounds in your answer. [3 marks]
- June 2023, Paper 3, Q15 (1 mark): What happens when water is vaporised? [1 mark] A Covalent bonds break within molecules. B Intermolecular forces are overcome. C The enthalpy of the molecules de
- June 2023, AS Paper 2, Q06.3 (2 marks): Explain why tetrachloromethane has a higher boiling point than dichloromethane. [2 marks]
- June 2023, AS Paper 2, Q06.4 (2 marks): Propan-1-ol has a higher boiling point than the other two compounds because of hydrogen bonding. Describe the hydrogen bonding in propan-1-ol. [2 marks]
- June 2022, AS Paper 1, Q04.1 (3 marks): Complete the diagram to show how one molecule of ammonia can form a hydrogen bond with one molecule of ethanol. Include all lone pairs of electrons and partial
- June 2022, AS Paper 1, Q04.5 (3 marks): Suggest, in terms of the intermolecular forces for each compound, why CBr4 has a higher boiling point than CHBr3 [3 marks]
- June 2022, AS Paper 2, Q13 (1 mark): Which compound has the highest boiling point? [1 mark] A CH3COCH2CH3 B CH3CH2CH2CH2OH C CH3CH2CH2CHO D CH3CH2CH2CH2CH3
- November 2021, Paper 3, Q17 (1 mark): Which statement about (CH3)2CHCH2COOH is correct? [1 mark] A In aqueous solution it reacts with magnesium to form carbon dioxide. B It can form hydrogen bonds.
- November 2021, AS Paper 1, Q05.1 (3 marks): Chlorine has a low boiling point because the forces between the molecules are weak. Explain how these forces arise between molecules of chlorine. [3 marks]
- November 2021, AS Paper 2, Q03.4 (3 marks): Explain why propanone has a lower boiling point than propan-2-ol. [3 marks]
- November 2020, Paper 1, Q07 (6 marks): The melting point of XeF4 is higher than the melting point of PF3 Explain why the melting points of these two compounds are different. In your answer you should
- November 2020, AS Paper 1, Q11 (1 mark): Which compound has hydrogen bonding? [1 mark] A NaH B NH3 C HI D SiH4
- November 2020, AS Paper 2, Q04.1 (3 marks): The boiling point of pentan-2-ol is 119 °C The boiling point of pent-1-ene is 30 °C Explain why pentan-2-ol has a higher boiling point than pent-1-ene. [3 marks
- June 2019, Paper 1, Q08.1 (3 marks): Draw a diagram to show the strongest type of interaction between two molecules of ethanol (C2H5OH) in the liquid phase. Include all lone pairs and partial charg
- June 2019, Paper 1, Q08.2 (3 marks): Methoxymethane (CH3OCH3) is an isomer of ethanol. Table 5 shows the boiling points of ethanol and methoxymethane. Table 5 Compound Boiling point / °C ethanol 78
- June 2019, Paper 2, Q07.2 (6 marks): Explain how and why isomers X and Y can be distinguished by comparing each of their • boiling points • 13C NMR spectra • infrared spectra. Use data from Tables
- June 2019, AS Paper 1, Q13 (1 mark): Which change occurs when water is vaporised? [1 mark] A An exothermic change occurs. B Covalent bonds are broken. C Intermolecular forces are overcome. D The to
- June 2019, AS Paper 2, Q05.1 (3 marks): Draw a diagram to show how two methanol molecules interact with each other through hydrogen bonding in the liquid phase. Include all partial charges and all lon
- June 2019, AS Paper 2, Q21 (1 mark): Which compound has the highest boiling point? [1 mark] A CH3CH2CH2Br B CH3CH2CH2F C CH3CH2CHO D CH3CH2COOH
- June 2018, Paper 2, Q03.1 (3 marks): Explain, with reference to intermolecular forces, why distillation allows propanal to be separated from the other organic compounds in this reaction mixture. [3
- June 2018, AS Paper 1, Q09.3 (3 marks): Silicon tetrafluoride (SiF4) is a tetrahedral molecule. Deduce the type of intermolecular forces in SiF4 Explain how this type of intermolecular force arises an
- June 2018, AS Paper 2, Q04.2 (2 marks): Explain why nonane has a higher boiling point than 2,4-dimethylheptane. [2 marks]
- June 2018, AS Paper 2, Q13 (1 mark): Which compound has the highest boiling point? [1 mark] A butanal B butan-2-ol C but-2-ene D 1-fluorobutane
- June 2017, Paper 3, Q05 (1 mark): Which compound has the highest boiling point? [1 mark] A CH3CH2CH2OH B CH3CH2CHO C CH3COCH3 D CH3COOCH3
- June 2017, AS Paper 1, Q05.2 (2 marks): Explain how permanent dipole-dipole forces arise between hydrogen chloride molecules. [2 mark
- June 2017, AS Paper 2, Q07.5 (6 marks): Cyclohexene is prepared by the dehydration of cyclohexanol using concentrated phosphoric acid as a catalyst. The structure of concentrated phosphoric acid is sh
- June 2017, AS Paper 2, Q09.1 (2 marks): Chloroethene has a melting point of −154 ºC All types of PVC melt at temperatures over 100 ºC Explain why PVC melts at a higher temperature than chloroethene. [
- June 2016, AS Paper 2, Q04.3 (6 marks): Predict the relative boiling points of these three compounds from the highest to the lowest boiling points. Justify this order in terms of intermolecular forces
- Specimen, Paper 1, Q05.3 (4 marks): Diagram Explanation
- Specimen, Paper 2, Q04.6 (1 mark): List alcohol A, product B and isomer C in order of increasing boiling point. [1 mark] 0 4 . 6
- Specimen, Paper 2, Q05.2 (4 marks): 5
- Specimen, Paper 3, Q01.4 (2 marks): Use your knowledge of structure and bonding to explain why it is possible to separat ethanal in this way. [2 mark 0 1 . 4
- Specimen, Paper 3, Q32 (1 mark): Which compound has the highest boiling point? [1 mark] A C2H4 B C2H6 C CH3NH2 D CH F 3 2 3
- June 2016, CHEM1 (old spec), Q2(a) (3 marks): Van der Waals’ forces exist between all molecules. Explain how these forces arise. [3 marks]
- June 2016, CHEM1 (old spec), Q2(b)(i) (3 marks): Explain, in terms of their intermolecular forces, why the boiling points of these compounds are different. [3 marks]
- June 2016, CHEM1 (old spec), Q2(b)(ii) (1 mark): Suggest how a mixture of methanol and methanethiol could be separated. [1 mark]
- June 2016, CHEM1 (old spec), Q2(c) (2 marks): Suggest why methaneselenol (CH3SeH) has a higher boiling point than methanethiol (CH3SH). [2 marks]
- June 2015, CHEM1 (old spec), Q5(b)(i) (1 mark): State the strongest type of interaction that occurs between molecules of hydrogen peroxide and water. [1 mark]
- June 2015, CHEM1 (old spec), Q5(b)(ii) (3 marks): Draw a diagram to show how one molecule of hydrogen peroxide interacts with one molecule of water. Include all lone pairs and partial charges in your diagram. [
- June 2015, CHEM1 (old spec), Q5(c) (2 marks): Explain, in terms of electronegativity, why the boiling point of H2S2 is lower than H2O2. [2 marks]
- June 2014, CHEM4 (old spec), Q4(a) (1 mark): Name the strongest type of interaction between polymer chains of Kevlar. [1 mark]
- June 2014, CHEM1 (old spec), Q4(a)(i) (1 mark): Name the strongest attractive force between two ammonia molecules. [1 mark]
- June 2014, CHEM1 (old spec), Q4(a)(ii) (3 marks): Draw a diagram to show how two ammonia molecules interact with each other in the liquid phase. Include all partial charges and all lone pairs of electrons in yo
- June 2014, CHEM1 (old spec), Q5(d)(iii) (2 marks): Explain why the melting point of dodecane is higher than the melting point of the straight-chain alkane produced by cracking dodecane. [2 marks]
- June 2013, CHEM1 (old spec), Q4(a) (1 mark): State the strongest type of intermolecular force between one molecule of ammonia and one molecule of water. (1 mark)
- June 2013, CHEM1 (old spec), Q4(b) (3 marks): Draw a diagram to show how one molecule of ammonia is attracted to one molecule of water. Include all partial charges and all lone pairs of electrons in your di
- June 2013, CHEM1 (old spec), Q4(c) (1 mark): Phosphine (PH3) has a structure similar to ammonia. In terms of intermolecular forces, suggest the main reason why phosphine is almost insoluble in water. (1 ma
- June 2013, CHEM1 (old spec), Q8(a) (3 marks): The structure of the bromoalkane Z is Give the IUPAC name for Z. Give the general formula of the homologous series of straight-chain bromoalkanes that contains
- June 2013, CHEM2 (old spec), Q6(c) (2 marks): Explain why chlorine has a lower boiling point than bromine.
- January 2013, CHEM1 (old spec), Q4(b) (1 mark): Both C3H8 and C4H10 can be liquefied and used as fuels for camping stoves. Suggest, with a reason, which of these two fuels is liquefied more easily. (1 mark)
- January 2013, CHEM1 (old spec), Q4(f)(iii) (2 marks): Ethanethiol and ethanol molecules have similar shapes. Explain why ethanol has the higher boiling point.
- January 2013, CHEM1 (old spec), Q4(g)(ii) (2 marks): X has a boiling point of 9.5 ºC. Explain why the boiling point of X is lower than that of its straight-chain isomer.
- June 2012, CHEM5 (old spec), Q1(c) (2 marks): Explain why phosphorus(V) oxide has a higher melting point than sulfur(VI) oxide.
- June 2012, CHEM1 (old spec), Q2(e) (2 marks): Explain why the boiling points of X and Y are similar.
- June 2012, CHEM1 (old spec), Q3(d) (1 mark): Although phosphine molecules contain hydrogen atoms, there is no hydrogen bonding between phosphine molecules. Suggest an explanation for this. (1 mark)
- January 2012, CHEM4 (old spec), Q8(b)(iii) (2 marks): Explain why the polymer in part (b) (ii) has a higher melting point than the polymer in part (b) (i). (2 marks)
- January 2012, CHEM5 (old spec), Q2(b) (2 marks): Use your knowledge of bonding to explain why ΔH is positive for this process. (2 marks)
- January 2012, CHEM5 (old spec), Q3(a)(ii) (2 marks): sulfur dioxide has a low melting point.
- January 2012, CHEM5 (old spec), Q3(b) (2 marks): Explain why the melting point of P4O10 is higher than the melting point of SO2
- January 2012, CHEM1 (old spec), Q1(d)(i) (1 mark): State the strongest type of intermolecular force between hydrogen fluoride molecules. (1 mark)
- January 2012, CHEM1 (old spec), Q1(d)(ii) (3 marks): Draw a diagram to show how two molecules of hydrogen fluoride are attracted to each other by the type of intermolecular force that you stated in part (d) (i). I
- January 2012, CHEM1 (old spec), Q1(e) (2 marks): The boiling points of fluorine and hydrogen fluoride are –188 oC and 19.5 oC respectively. Explain, in terms of bonding, why the boiling point of fluorine is ve
- June 2011, CHEM4 (old spec), Q4(a)(ii) (3 marks): In terms of the intermolecular forces between the polymer chains, explain why polyamides can be made into fibres suitable for use in sewing and weaving, whereas
- June 2011, CHEM1 (old spec), Q3(a) (2 marks): Explain why iodine has a higher melting point than fluorine. (2 marks)
- June 2011, CHEM1 (old spec), Q3(c) (1 mark): State the strongest type of intermolecular force in a sample of NHF2 (1 mark)
- January 2011, CHEM1 (old spec), Q1(a) (1 mark): The following diagram shows the arrangement of some of the water molecules in a crystal of ice. With reference to the structure shown above give one reason why
- January 2011, CHEM1 (old spec), Q1(b)(i) (1 mark): State the strongest type of intermolecular force holding the water molecules together in the ice crystal. (1 mark)
- January 2011, CHEM1 (old spec), Q1(b)(ii) (1 mark): State the strongest type of intermolecular force in methane. (1 mark)
- January 2011, CHEM1 (old spec), Q1(b)(iii) (1 mark): Give one reason why the melting point of ice is higher than the melting point of methane. (1 mark)
- January 2011, CHEM1 (old spec), Q6(d) (2 marks): Suggest why the branched chain isomer shown above has a lower boiling point than octane.
- June 2010, CHEM1 (old spec), Q1(c) (1 mark): Suggest the strongest type of intermolecular force between CCI2F2 molecules. (1 mark)
- June 2010, CHEM1 (old spec), Q7(c) (2 marks): Explain why iodine vaporises when heated gently.
- January 2010, CHEM1 (old spec), Q3(a) (2 marks): State the strongest type of intermolecular force in water and in hydrogen sulfide (H2S). Water Hydrogen sulfide (2 marks)
- January 2010, CHEM1 (old spec), Q3(b) (3 marks): Draw a diagram to show how two molecules of water are attracted to each other by the type of intermolecular force you stated in part (a). Include partial charge
- January 2010, CHEM1 (old spec), Q3(c) (1 mark): Explain why the boiling point of water is much higher than the boiling point of hydrogen sulfide. (1 mark)
- January 2010, CHEM1 (old spec), Q3(d) (2 marks): Explain why the boiling points increase from H2S to H2Te (2 marks)
- June 2009, CHEM1 (old spec), Q3(a)(ii) (2 marks): 3 (a) (ii) State the strongest type of intermolecular force present in each compound. Liquid ethanol Liquid propane (2 marks)
- June 2009, CHEM1 (old spec), Q3(b) (3 marks): 3 (b) Ethanol dissolves in water. Draw a diagram to show how one molecule of ethanol interacts with one molecule of water in the solution. Include partial charg
- June 2009, CHEM1 (old spec), Q4(d)(i) (2 marks): 4 (d) (i) Explain the trend in these boiling points. (2 marks)
- June 2009, CHEM2 (old spec), Q3(b) (1 mark): 3 (b) The students deduced that the heat change was due only to the formation of intermolecular forces between ethyl ethanoate molecules and trichloromethane mo
- January 2009, CHEM1 (old spec), Q2(b) (2 marks): 2 (b) State the strongest type of intermolecular force in the following compounds. Methane (CH4) Ammonia (NH3) (2 marks)
- January 2009, CHEM1 (old spec), Q2(c) (3 marks): 2 (c) Use the values in the table to explain how the strongest type of intermolecular force arises between two molecules of ammonia. (3 marks)
- January 2009, CHEM1 (old spec), Q2(f) (1 mark): 2 (f) The boiling point of AsH3 is –62.5 °C and the boiling point of NH3 is –33.0 °C. Suggest why the boiling point of AsH3 is lower than that of NH3 (1 mark)
- January 2009, CHM1 (2008 spec), Q3(b) (2 marks): 3 (b) Explain the heat energy change associated with boiling. (2 marks)
- January 2009, CHM1 (2008 spec), Q3(c)(i) (2 marks): 3 (c) (i) Define the term electronegativity. (2 marks)
- January 2009, CHM1 (2008 spec), Q3(c)(ii) (2 marks): 3 (c) (ii) Explain, in terms of electronegativity, why hydrogen bonds form between H2O molecules but not between H2S molecules. (2 marks)
- January 2009, CHM1 (2008 spec), Q3(c)(iii) (1 mark): 3 (c) (iii) Explain, in terms of the intermolecular forces present, why the boiling point of H2S is so much lower than that of H2O (1 mark)
- January 2009, CHM1 (2008 spec), Q3(c)(iv) (1 mark): 3 (c) (iv) Identify an element, other than oxygen, that when bonded to hydrogen can be involved in hydrogen bonding. (1 mark)
- January 2009, CHM1 (2008 spec), Q3(d) (3 marks): 3 (d) Draw a diagram to show how two molecules of water are attracted to each other by hydrogen bonding. Include partial charges and all lone pairs of electrons
- January 2009, CHM1 (2008 spec), Q5(a)(i) (3 marks): 5 (a) (i) Describe the structure of, and the bonding in, solid iodine. (3 marks)
- January 2009, CHM1 (2008 spec), Q5(a)(ii) (2 marks): 5 (a) (ii) Explain the trend in the melting points of the halogens shown in the table above. (2 marks)
- June 2008, CHM5 (2008 spec), Q2(d) (3 marks): 2 (d) Explain in terms of intermolecular forces why the enthalpy of vaporisation for liquid hydrogen fluoride is greater than that for liquid ammonia. (3 marks)
- January 2008, CHM1 (2008 spec), Q3(d) (6 marks): (d) The boiling points of some hydrogen halides are shown in the table below. Explain, in terms of the intermolecular forces present, why Hydrogen halide HF HCl
- January 2008, CHM4 (2008 spec), Q5(d) (2 marks): (d) (i) Name the strongest type of intermolecular force in polymer R. (ii) Name the strongest type of intermolecular force in polymer T. (2 marks)
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