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ID: past-exam-of-the-chemistry-course-of-the-year-3-of-the-natural-sciences-course-of-the-university-of-cambridge/2022/paper-3/39/b/solution

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Past exam of the chemistry course of the year 3 of the natural sciences course of the University of Cambridge / 2022 / Paper 3 / 39 / b / Solution by Codex 0 2026-10-20
Figure 1.
Proton letters and carbon numbers assigned to the two side chains
. Details.
On the ester-containing side chain, read outward from the cyclohexene:
(1)
A is the downfield beta-vinylic proton and D the alpha-vinylic proton next to the ester.
The phenyl ortho pair is B on carbon 7; the meta pair is C on carbon 6; its para proton is the remaining C on carbon 5. Thus the C envelope integrates to three protons, while B integrates to two. Carbon 3 is the unprotonated ipso site.
In the other substituent, 10 is the quaternary C-OH carbon. The methyl assignments are N on 13 and O on 16, reading the very closely spaced HSQC cross peaks together with the positive methyl responses in DEPT-135. Their mutual long-range correlations and correlations to 10 support the gem-dimethyl group. The two methyl carbons are distinguishable in this chiral molecular environment; their exact stereotopic names are not determined here.
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