Edexcel A-Level Chemistry AS Paper 1, June 2025: Question 3

2 marks · Medium difficulty · Multiple Choice

Identify intermolecular forces present in water and explain the difference in water solubility between ethanol and ethanethiol.

Practise this question

Question

Question 3 consists of two multiple-choice questions on intermolecular forces. Part (a) asks for the intermolecular forces between water molecules, with options A (hydrogen bonds only), B (London forces and permanent dipoles only), C (London forces, permanent dipoles and hydrogen bonds), and D (permanent dipoles and hydrogen bonds only). Part (b) states that ethanol is soluble in water but ethanethiol is almost insoluble, and asks for the best explanation, with four options comparing London forces, electronegativity, hydrogen bonding, and dipole moments.

Mark scheme

Show the mark scheme Mark scheme for Question 3 showing the answers. For 3(a), the correct answer is C (London forces, permanent dipoles and hydrogen bonds), noting that A, B, and D are incorrect because they omit one or more of the forces present. For 3(b), the correct answer is C (ethanol forms hydrogen bonds with water but ethanethiol does not), explaining that while statements A, B, and D may be factually correct, they do not explain the solubility difference.

How to answer it

Intermolecular Forces and Aqueous Solubility

📌 What this question tests

This question evaluates your foundational understanding of intermolecular interactions in covalent molecular substances, specifically:

  • Recognising the cumulative nature of intermolecular forces in polar, hydrogen-bonding substances like water (H₂O).
  • Applying intermolecular force theory to explain comparative aqueous solubility (ethanol vs. ethanethiol).
  • Distinguishing between chemically true statements and the best direct explanation for a physical phenomenon.
Part (a) • 1 Mark

Intermolecular Forces Between Water Molecules

Question: What are the intermolecular forces between water molecules?

✅ Correct Answer

C: London forces, permanent dipoles and hydrogen bonds

Mark Breakdown:
[1 mark] Awarded exclusively for selecting option C.

💡 Key Knowledge

  • London forces (dispersion forces): Present between all atoms and molecules due to temporary fluctuations in electron density causing instantaneous induced dipoles.
  • Permanent dipole-dipole forces: Present because H₂O has a non-linear (bent) shape and asymmetrical charge distribution (O is much more electronegative than H).
  • Hydrogen bonding: An especially strong type of permanent dipole attraction occurring because H is directly bonded to the highly electronegative oxygen atom with lone pairs.

❌ Common Errors & Misconceptions

  • Selecting Option A (Hydrogen bonds only): The most common student error. Students remember water forms strong hydrogen bonds and forget that London forces exist in every molecular system without exception.
  • Treating hydrogen bonding as mutually exclusive: Hydrogen bonding is simply an exceptionally strong category of permanent dipole attraction; it does not replace or cancel out underlying London forces or basic permanent dipole interactions.

🧠 Exam Technique

Whenever an exam asks "What forces exist between molecules?", start from the bottom up:

  1. Does it have electrons? → Always has London forces.
  2. Is the molecule polar? → Also has permanent dipoles.
  3. Is H bonded to N, O, or F with lone pairs available? → Also forms hydrogen bonds.
Part (b) • 1 Mark

Explaining Solubility: Ethanol vs. Ethanethiol

Question: Which is the best explanation for why ethanol is soluble in water, but ethanethiol is almost insoluble?

✅ Correct Answer

C: ethanol forms hydrogen bonds with water but ethanethiol does not

Mark Breakdown:
[1 mark] Awarded exclusively for selecting option C.

💡 Key Knowledge

  • For a covalent compound to dissolve well in water, the energy released when forming new solute-solvent interactions must be sufficient to compensate for breaking the strong hydrogen bonds between water molecules.
  • The -O-H group in ethanol (CH₃CH₂OH) readily forms hydrogen bonds with water molecules.
  • Although sulfur has lone pairs, it is not electronegative enough to participate in hydrogen bonding. Hence, ethanethiol (CH₃CH₂SH) can only form weak London and dipole-dipole forces with water, which cannot overcome the water-water hydrogen bonds.

❌ The "True Statement" Distractor Trap

The examiner intentionally included statements that are factually correct, but do not provide the underlying chemical explanation for solubility:

  • Option B ("sulfur is less electronegative than oxygen"): This is true, but it is an atomic property, not the direct intermolecular reason that explains dissolution into solvent water.
  • Option A: Ethanethiol actually has more electrons than ethanol, so its London forces are indeed stronger, but stronger London forces would favour mixing rather than explain insolubility!
  • Option D: Ethanol does have a larger dipole, but this is an incomplete explanation because simple dipole interactions are not strong enough to disrupt the hydrogen-bonded network of water.

🧠 Examiner Advice

When an Edexcel question asks for the "best explanation" regarding solubility in water:

  • Always focus directly on hydrogen bonding to water.
  • Remember the strict criteria for H-bonding: Hydrogen must be covalently bonded to Nitrogen, Oxygen, or Fluorine (N, O, F). Sulfur does not form hydrogen bonds!

Topics

Physical Chemistry · Topic 2: Bonding and Structure

Question and mark scheme from the Edexcel A-Level Chemistry examination, AS Paper 1, June 2025. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.