Chapter 12: PROBLEM 12.22 (page 476)
Question: Draw the products formed when each alkyne is treated with O3 followed by H2O .
a.

b.

c.

Short Answer
Answer
a.

b. A biphenyl compound upon ozonolysis gives the same compound, that is

c.

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Chapter 12: PROBLEM 12.22 (page 476)
Question: Draw the products formed when each alkyne is treated with O3 followed by H2O .
a.

b.

c.

Answer
a.

b. A biphenyl compound upon ozonolysis gives the same compound, that is

c.

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Question: Given that syn addition of H2 occurs from both sides of a trigonal planar double bond, draw all stereoisomers formed when each alkene is treated with H2 .
a.

b.

c.

Question: a) Draw the structure of a compound of molecular formula C6H10 that reacts with H2 in the presence of Pd-C but does not react with H2in the presence of Lindlar catalyst. (b) Draw the structure of a compound of molecular formula C6H10 that reacts with H2 when either catalyst is present
Question: A chiral alkyne A with molecular formula C6H10 is reduced with and Lindlar catalyst to B having the R configuration at its stereogeniccentre. What are the structures of A and B?
Question: Match each alkene to its heat of hydrogenation.Alkenes: 3-methylbut-1-ene, 2-methylbut-1-ene, 2-methylbut-2-ene (hydrogenation) kJ/mol: –119, –127, –112
Question: What is the structure of cis-jasmone, a natural product isolated from jasmine flowers, formed by the treatment of alkyne A with H2in the presence of the Lindlar catalyst?

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