Chapter 22: Q70P-A (page 1204)
Question: Predict the products of these reaction sequences.
a.
Short Answer
Answer
Chapter 22: Q70P-A (page 1204)
Question: Predict the products of these reaction sequences.
a.
Answer
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Get started for freeThe following compounds can be synthesized by aldol condensations, followed by further reactions. (In each case, work backward from the target molecule to an aldol product, and show what compounds are needed for the condensation.)
Propose a mechanism for the conjugate addition of a nucleophile (Nuc:-) to acrylonitrile (H2C=CHCN) and to nitroethylene. Use resonance forms to show how the cyano and nitro groups activate the double bond toward conjugate addition.
Question:Show how you would use the Robinson annulation to synthesize the following compounds.
C.
The following compound results from base-catalyzed aldol cyclization of a 2-substituted cyclohexanone.
Show how you would accomplish the following conversions in good yields. You may use any necessary reagents.
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