Chapter 12: PROBLEM 12.44 (page 489)
Question: What alkene is needed to synthesize each 1,2-diol using [1] followed by NAHSO3 in H2O ; or [2] CH3CO3H followed by -OH in H2O ?
a.

b.

c.

Short Answer
Answer
a.

b.

c.

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Chapter 12: PROBLEM 12.44 (page 489)
Question: What alkene is needed to synthesize each 1,2-diol using [1] followed by NAHSO3 in H2O ; or [2] CH3CO3H followed by -OH in H2O ?
a.

b.

c.

Answer
a.

b.

c.

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Question: Draw the organic products formed when each alkene is treated with H2 / Pd-C. Indicate the three-dimensional structure of all stereoisomers formed.
a.

b.

c.

Question:Devise a synthesis of (3R,4S)-3,4-dichlorohexane from acetylene and any needed organic compounds or inorganic reagents.
Question: Draw all alkenes that react with one equivalent of H2 in the presence of a palladium catalyst to form each alkane. Consider constitutional isomers only
a.

b.

c.

Question: Devise a synthesis of muscalure, the sex pheromone of the common housefly, from acetylene and any other required reagents.

Muscalure
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?

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