Astatine is a halogen found below iodine in Group 7. A student states: 'Astatine must be a better oxidising agent than iodine and will displace iodine from a solution of potassium iodide.' Evaluate the student's statement.

AQA A-Level Chemistry (7405) — 3.2.3 Group 7(17), the halogens · Evaluate · 5 marks · View as Markdown

Written & reviewed by James Millett — Biology (Imperial College London), PGCE Science (University of Cambridge).

Model answer (5 marks)

Astatine is a worse oxidising agent than iodine.
1. Oxidising ability decreases down Group 7 because the outermost electrons are further from the nucleus.
2. Greater distance means increased shielding and a weaker effective nuclear charge.
3. Consequently astatine attracts or gains an electron less readily than iodine.
4. Therefore astatine would not displace iodine from a potassium iodide solution.
5. The student’s conclusion is therefore incorrect.

Examiner tips

  • Use the term ‘oxidising agent’ and ‘displace’ explicitly.
  • Show the trend of decreasing oxidising power down the group.
  • Explain the role of shielding and effective nuclear charge.
  • State the final verdict clearly.

Common mistakes

  • Assuming astatine is more reactive because it is heavier.
  • Forgetting to mention shielding/effective nuclear charge.
  • Claiming astatine would displace iodine without justification.

Mark scheme (5 marks)

  1. Astatine is a worse (less powerful) oxidising agent than iodine, not a better one
  2. Oxidising ability / reactivity decreases going down Group 7
  3. Because the outer shell / outermost electrons are further from the nucleus in astatine than in iodine
  4. So astatine attracts / gains an electron less easily than iodine (increased shielding / less effective nuclear attraction)
  5. Therefore astatine would NOT displace iodine from potassium iodide solution — the student's conclusion is incorrect

Key terms in this question

oxidising agent · Group 7

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