Chapter 10: Q.8. (page 390)
Question: Draw the structure corresponding to each IUPAC name.
a. (Z)-4-ethylhept-3-ene
b. (E)-3,5,6-trimethyloct-2-ene
c. (Z)-2-bromo-1-iodohex-1-ene
Short Answer
Answer
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Chapter 10: Q.8. (page 390)
Question: Draw the structure corresponding to each IUPAC name.
a. (Z)-4-ethylhept-3-ene
b. (E)-3,5,6-trimethyloct-2-ene
c. (Z)-2-bromo-1-iodohex-1-ene
Answer
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Question: Label each C-C double bond as E or Z. Kavain is a naturally occurring relaxant isolated from kava root.
Question: Less stable alkenes can be isomerized to more stable alkenes by treatment with strong acid. For example, 2,3-dimethylbut-1-ene is converted to 2,3-dimethylbut-2-ene when treated with . Draw a stepwise mechanism for this isomerization process.
Question: Explain why the addition of HBr to alkenes A and C is regioselective, forming addition products B and D, respectively.

Question: Draw a stepwise mechanism for the following reaction, which results in ring expansion of a six-membered ring to a seven-membered ring.

Question: Treatment of 3-methylcyclohexene with HCl yields two products, 1-chloro-3-methylcyclohexane and 1-chloro-1-methylcyclohexane. Draw a mechanism to explain this result.
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