Chapter 24: Q.10. (page 962)
Question: What carbonyl starting materials are needed to prepare each compound using a directed aldol reaction?
Short Answer
Answer
a.
b.
c.
Chapter 24: Q.10. (page 962)
Question: What carbonyl starting materials are needed to prepare each compound using a directed aldol reaction?
Answer
a.
b.
c.
All the tools & learning materials you need for study success - in one app.
Get started for freeQuestion: Avobenzone is a conjugated compound that absorbs ultraviolet light with wavelengths in the 320–400 nm region, so it is a common ingredient in commercial sunscreens. Write out two different crossed Claisen reactions that form avobenzone.
Question: Draw the product formed in each directed aldol reaction.
Question: Draw a stepwise mechanism for the following Robinson annulation. This reaction was a key step in a synthesis of the steroid cortisone by R. B. Woodward and co-workers at Harvard University in 1951.
Question: Devise a stepwise mechanism for the following reaction, a key step in the synthesis of the antibiotic abyssomicin C. Abyssomicin C was isolated from sediment collected from almost 1000 ft below the surface in the Sea of Japan. (Hint: The mechanism begins with a Dieckmann reaction.)
Question: Which carbonyl compounds do not undergo an aldol reaction when treated with OH- in H2O ?
What do you think about this solution?
We value your feedback to improve our textbook solutions.