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Chemistry, 21.04.2020 17:49 ninaaforever

The ring expansion (above) proceeds from an initial enolate 1 which undergoes an intramolecular aldol reaction to give intermediate 2. then undergoes a retro-aldol reaction to give enolate 3. A final protonation gives the product. Write a detailed mechanism for this reaction on paper, then draw structural formulas for intermediate 2 and enolate 3 in the window below.

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The ring expansion (above) proceeds from an initial enolate 1 which undergoes an intramolecular aldo...
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