Solution

ID: past-exam-of-the-chemistry-course-of-the-year-4-of-the-natural-sciences-course-of-the-university-of-cambridge/2022/paper-1/8/a/i/solution

The carbon–phosphorus coupling in the C spectrum is consistent with deprotonation of the methyl group rather than loss of that group:
Addition to the nitrile initially gives . An intramolecular proton transfer then converts the imidoyl anion into a conjugated lithiated enamide:
The phosphorus–carbon bond is retained. The rearrangement is a hydrogen migration, not a migration of the phosphoryl group to nitrogen. Addition of half an equivalent of TMEDA per Li gives the hemisolvated dimer
The tetrameric and dimeric nuclearities are established for this reaction system; the spectra in the question are consistent with them, but spectra alone would not uniquely prove every detail of the aggregates.[ref]

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