Chapter 12: PROBLEM 12.12 (page 466)
Question: What product is formed when is treated with each reagent: (a) H2 (excess), Pd-C; ; (b) H2(1 equiv), Lindlar catalyst; (c) H2(excess), Lindlar catalyst; (d) Na,NH3 ?
Short Answer
Answer
a.

b.

c.

d.

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Chapter 12: PROBLEM 12.12 (page 466)
Question: What product is formed when is treated with each reagent: (a) H2 (excess), Pd-C; ; (b) H2(1 equiv), Lindlar catalyst; (c) H2(excess), Lindlar catalyst; (d) Na,NH3 ?
Answer
a.

b.

c.

d.

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Question: In the oxidation of cyclohexanols, it is generally true that sterically hindered alcohols react faster than unhindered alcohols. Which of the following alcohols should be oxidized more rapidly?

Question: Draw the products of each Sharpless epoxidation.
a.

b.

Question: Draw the organic products in each of the following reactions.
a.

b.

c.

d.

Question: What allylic alcohol and DET isomer are needed to make each chiral epoxide using a sharpless asymmetric epoxidation reaction?
Question: Draw the products formed when each diene is treated with O3 followed by CH3SCH3.
a.

b.

c.

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