Chapter 12: PROBLEM 12.50 (page 490)
Question: Identify the starting material in each reaction.
a.
b.
Short Answer
Answer
a.
b.
Chapter 12: PROBLEM 12.50 (page 490)
Question: Identify the starting material in each reaction.
a.
b.
Answer
a.
b.
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Get started for freeQuestion: Identify A in the following reaction sequence and draw a mechanism for the conversion of A to B. B has been converted to (S,S)-reboxetine, an antidepressant marketed outside the United States.
Question: Devise a synthesis of muscalure, the sex pheromone of the common housefly, from acetylene and any other required reagents.
Muscalure
Question: What alkyne (or diyne) yields each set of oxidative cleavage products?
a.
b.
c.
d.
Question: Stearidonic acid (C18H28O2 ) is an unsaturated fatty acid obtained from oils isolated from hemp and blackcurrant (see also Problem 10.11).
a. What fatty acid is formed when Stearidonic acid is hydrogenated with excess H2 and a Pd catalyst?
b. What fatty acids are formed when stearidonic acid is hydrogenated with one equivalent of H2 and a Pd catalyst?
c. Draw the structure of a possible product formed when stearidonic acid is hydrogenated with one equivalent of H2 and a Pd catalyst, and one double bond is isomerized to a trans isomer.
d. How do the melting points of the following fatty acids compare: stearidonic acid; one of the products formed in part (b); the product drawn in part (c)?
Question: Dihydroxylation of an alkene can be carried out with in . In this reaction, transbut-2-ene affords (2R,3S)-butane-2,3-diol, whereas cis-but-2-ene affords a mixture of (2R,3R)-butane-2,3-diol and (2S,3S)-butane-2,3-diol. Does dihydroxylation by this method occur with syn or anti addition?
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