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Chapter 10: Q.23. (page 406)

Question: Draw the products of each reaction, including stereochemistry.

Short Answer

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Answer

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01

Halogenation

Halogenation involves the addition of halogen atoms on the double bond. It gives trans enantiomers through anti-addition.

02

Formation of products

a.

The reaction of cyclobutene with dibromide results in the formation of enantiomers. The reaction is shown below:

Formation of products in a

b.

The reaction of cyclobutene with 1-methylcyclohex-1-ene results in the formation of enantiomers. The reaction is shown below:

Formation of products in b

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Most popular questions from this chapter

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

Question: Calculate the number of degrees of unsaturation for each molecular formula.

a. C6H8

b. C40H56

c. C10H16O2

d. C8H9Br

e. C8H9ClO

f. C7H11N

g. C4H8BrN

h. C10H10ClNO

Question: Draw a stepwise mechanism for the conversion of hex-5-en-1-ol to the cyclic ether A.

Question: Use the Hammond postulate to explain why (CH3)2C=CH2reacts faster than CH3CH=CH2 in electrophilic addition of HX.

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

a.

b.

c.

d.
See all solutions

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