Chapter 25: 53 (page 1043)
Draw the products formed when each amine is treated with [1] (excess); [2] ; [3] . Indicate the major product when a mixture results.
a

b

c

d

Short Answer
a

b

c

d

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Chapter 25: 53 (page 1043)
Draw the products formed when each amine is treated with [1] (excess); [2] ; [3] . Indicate the major product when a mixture results.
a

b

c

d

a

b

c

d

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Devise a synthesis of each compound from the given starting material(s). Albuterol is a bronchodilator and proparacaine is a local anesthetic.
(a)

(b)

Explain the observed difference in the values of the conjugate acids of amines A and B.

Tertiary ( ) aromatic amines react with and HCl to afford products of electrophilic aromatic substitution. Draw a stepwise mechanism for this nitrosation reaction and explain why it occurs only on benzene rings with strong ortho, para activating groups.

Question: Draw a structure corresponding to each name.
a. 2,4-dimethylhexan-3-amine
b. N-methylpentan-1-amine
c. N-isopropyl-p-nitroaniline
d. N-methylpiperidine
e. N,N-dimethylethanaminef. 2-aminocyclohexanoneg. N-methylanilineh. m-ethylaniline
Question:The pKa of the conjugate acid of guanidine is 13.6, making it one of the strongest neutral organic bases. Offer an explanation.

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