Q5(b)(i). Three para-substituted styrenes in anionic polymerisation
Arrange the monomers I (p-methylstyrene), II (p-nitrostyrene) and III (p-methoxystyrene) in order of decreasing ability to undergo anionic polymerisation. [structures given in the paper]
Answer in brief
II > I > III (p-NO₂ > p-CH₃ > p-OCH₃).
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Coversanionic polymerisationsubstituted styrenebenzylic carbanionHammett sigmaelectron-withdrawing group
All parts of Question 5
- 5(a) Five ¹H NMR signals of pentane-2,4-dione10 marks
- 5(b)(i) Three para-substituted styrenes in anionic polymerisation5 marks
- 5(b)(ii) Structures and configurations of natural and synthetic rubber5 marks
- 5(c) Acetophenone with SeO₂; benzoic acid with Na in liquid NH₃10 marks
- 5(d) Ease of Norrish type II hydrogen abstraction in two groups of ketones10 marks
- 5(e) McLafferty rearrangement in pentan-2-one; base peak of pentan-3-one10 marks