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A-LevelChemistryPolymerisation9701/42 · May/June 2020 · Q612 Marks

The class of polymers called polycarbonates are made by the reaction of carbonyl dichloride, COCl₂, with a diol. a diol n HOROH + n COCl₂ → a polycarbonate [Polymer structure] + 2nHCl Nalgene® is a polycarbonate formed from the diol P and COCl₂. P [Structure of diol P]

  1. (a)(i)Deduce the type of polymerisation shown here.[1]
  2. (a)(ii)Draw one repeat unit of Nalgene®.[1]
  3. (a)(iii)Nalgene® is a strong and tough polymer. Identify two types of intermolecular force that are responsible for these properties of Nalgene®. 1 2[1]
  4. (b)Proteins are polymers of amino acids. Complete the table to show how the secondary and tertiary structures of proteins are stabilised. one intermolecular force responsible groups involved secondary structure tertiary structure[2]
  5. (c)Explain the significance of hydrogen bonding in DNA in relation to the accurate replication of genetic information.[2]
  6. (d)Many polymers are degradable. State two different processes by which some polymers can be degraded.[1]
  7. (e)(i)Draw the structures of the two other organic products formed.[2]
  8. (e)(ii)Using the 3-letter abbreviations for the amino acids as given in the Data Booklet, complete the sequence for the cyclic peptide, B. [Circular diagram with one "Thr" label][1]
  9. (e)(iii)Name two analytical techniques that could be used to separate these amino acids. and[1]

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Mark scheme

Marking points from the official mark scheme (May/June 2020). The mark or mark type is shown in brackets.

  1. [1] condensation
  2. [1] (See mark scheme for structure - repeat unit of polycarbonate from diol P and COCl₂)
  3. [1] id-id forces/London forces AND permanent dipole-dipole forces
  4. [2] M1 (secondary structure by) hydrogen bonding between CO and NH groups M2 (tertiary structure by) interactions between R groups and one example of a named intermolecular force
  5. [2] M1 (hydrogen bonding between) base pairs M2 A with T and C with G
  6. [1] hydrolysis and by action of light/UV
  7. [2] Structures of Phenylalanine (Phe) and Glycine (Gly) (See mark scheme for structures)
  8. [1] correct labelling as shown (e.g., Thr, Phe, Gly, Phe, Gly, Phe clockwise or counterclockwise starting from Thr)
  9. [1] electrophoresis and thin-layer / paper chromatography [1]

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About this question

Topic
Polymerisation, A-Level Chemistry (syllabus 9701). Structured question, 12 marks.
Source
A-Level Chemistry, May/June 2020 Paper 4 Variant 2, question 6.

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