Chapter 9: Q36 E (page 286)
Question: How would you carry out the following conversions? More than one
step may be needed in some instances.
Chapter 9: Q36 E (page 286)
Question: How would you carry out the following conversions? More than one
step may be needed in some instances.
All the tools & learning materials you need for study success - in one app.
Get started for freeThe oral contraceptive agent Mestranol is synthesized using a carbonyl addition reaction like that shown in Problem 9-50. Draw the structure of the ketone needed.
How would you prepare the following carbonyl compounds starting from an alkyne (reddish-brown Br)?
b.
The final step in the hydration of an alkyne under acidic conditions is the tautomerization of an enol intermediate to give the corresponding ketone. The mechanism involves a protonation followed by a deprotonation.
Show the mechanism for each of the following tautomerizations.
The pkaof acetone, CH3COCH3, is 19.3. Which of the following bases is strong enough to deprotonate acetone?
(b)
The sex attractant given off by the common housefly is an alkene named muscalure. Propose a synthesis of muscalure starting from acetylene and any alkyl halides needed. What is the IUPAC name for muscalure?
Muscalure
What do you think about this solution?
We value your feedback to improve our textbook solutions.