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Chapter 10: Q.30. (page 417)

Question: Draw the products of each reaction using the two-part strategy from Sample Problem 10.7.

Short Answer

Expert verified

Answer

a.

Step by step solution

01

Step 1:Addition reaction

There are many ways to convert the double bond into different products via an addition reaction. The reaction of an alkene with HBr and acid-catalyst hydration is an example of addition reaction.

02

Formation of products for a, b and c

a.

The reaction of methylenecyclohexane with HBr gives 1-bromo-1-methylcyclohexane as shown below:

Product formation in a

b.

NaOCH3 acts as a nucleophile as well as a base. The reaction of 2-chloropentane with NaOCH3 is shown below:

Product formation in b

c.

The reaction of 1-propylcyclohexanol with H2SO4 is shown below:

Product formation in c

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Most popular questions from this chapter

Question: Label each carbon-carbon double bond in 11-cis-retinal as E or Z. As we will learn in Section 21.11, the isomerization of one double bond in this compound to a less crowded stereoisomer takes place when light strikes the retina of the eye.

Question: Devise a synthesis of each compound from cyclohexene as the starting material. More than one step is needed.

a.

b.

c.

d.

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

Question: What three alkenes (excluding stereoisomers) can be used to prepare 3-chloro-3-methylhexane by addition of HCl?

Question: Name each of the following epoxides as an alkene oxide.

a.

b.

c.


d.
See all solutions

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