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PROBLEM 25.23

Page 1022

Question: Which N atom in each compound is more basic? What product is formed when each compound is treated with HCl?

a.

b.

PROBLEM 25.24

Page 1023

Question: Draw the products formed when each carbonyl compound reacts with the following amines:

1. CH3CH2CH2NH2

2.(CH3CH2)2NH

a.

b.

c.

PROBLEM 25.27

Page 1027

Question: Draw the product formed by treating each compound with excess CH3I , followed by Ag2O, and then heat.

a.

b.

c.

PROBLEM 25.28

Page 1027

Question: Draw the major product formed in each reaction.

a.

b.

c.

d.

PROBLEM 25.29

Page 1029

Question: Draw鈥倀he鈥俻roduct鈥俧ormed鈥倃hen鈥俥ach鈥俢ompound鈥俰s鈥倀reated鈥倃ith鈥侼aNO2鈥俛苍诲鈥侣颁濒.

a.

b.

c.

d.


PROBLEM 25.30

Page 1033

Question: Draw the product formed in each reaction.

a.

b.

c.

d.

PROBLEM 25.33

Page 1035

Question: What starting materials are needed to synthesize each azo compound?

a.

b.

PROBLEM 25.35

Page 1041

Question: Give a systematic or common name for each compound.

PROBLEM 25.65

Page 1045

Question: Devise a synthesis of each compound from benzene. You may use any other organic or inorganic reagents.

a.

b.

c.

d.

e.

f.

PROBLEM 25.68

Page 1046

Question: Safrole, which is isolated from sassafras (Problem 21.33), can be converted to the illegal stimulant MDMA (3,4-methylenedioxymethamphetamine, 鈥淓cstasy鈥) by a variety of methods. (a) Devise a synthesis that begins with safrole and uses a nucleophilic substitution reaction to introduce the amine. (b) Devise a synthesis that begins with safrole and uses reductive amination to introduce the amine.

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