Chapter 22: Q.69-G (page 1204)
Question: Predict the products of the following reactions
g.
Short Answer
Answer
Chapter 22: Q.69-G (page 1204)
Question: Predict the products of the following reactions
g.
Answer
All the tools & learning materials you need for study success - in one app.
Get started for freeQuestion:Show how you would use the Robinson annulation to synthesize the following compounds.
C.
When cyclodecane-1,6-dione is treated with sodium carbonate, the product gives a UV spectrum similar to that of 1-acetyl-2-methylcyclopentene. Propose a structure for the product, and give a mechanism for its formation.
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 an aldol, Claisen, or another type of condensation to make each compound.
a.
Biochemists studying the structure of collagen (a fibrous protein in connective tissue) found cross-links containing unsaturated aldehydes between protein chains. Show the structures of the side chains that react to form these crosslinks, and propose a mechanism for their formation in a weakly acidic solution.
What do you think about this solution?
We value your feedback to improve our textbook solutions.