a. Identify all electrophilic sites in chloroacetyl chloride. b. Give the product that forms if dimethylaniline reacts with each of the electrophilic sites in chloroacetyl chloride. c. Assuming that the yield of your amidation reaction (the first step of this synthesis) was 100%, how many mole equivalents of diethylamine are you using in the second step of this synthesis? d. Indicate two differences between the IR spectra of lidocaine (3) and 2,6-dimethylaniline (1). e. Explain how you will be able to tell that the second step of the synthetic route was successfu

Introduction to General, Organic and Biochemistry
11th Edition
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Chapter31: Immunochemistry
Section: Chapter Questions
Problem 31.75P
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a. Identify all electrophilic sites in chloroacetyl chloride.
b. Give the product that forms if dimethylaniline reacts with each of the electrophilic sites in chloroacetyl
chloride.
c. Assuming that the yield of your amidation reaction (the first step of this synthesis) was 100%, how many
mole equivalents of diethylamine are you using in the second step of this synthesis?
d. Indicate two differences between the IR spectra of lidocaine (3) and 2,6-dimethylaniline (1).
e. Explain how you will be able to tell that the second step of the synthetic route was successful.

CH3
CH3
NH₂
En L E
CH3
CH3
NaO CH3
1
2
CH3 CH3
(excess)
CH3
CH3
3
CH3
CH3
Transcribed Image Text:CH3 CH3 NH₂ En L E CH3 CH3 NaO CH3 1 2 CH3 CH3 (excess) CH3 CH3 3 CH3 CH3
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