Aromatic molecules that differ from benzene can also undergo EAS reaction. Shown below, is an example. CH3 NO₂+ CH3 CH3 N & d -NO₂ NO₂ B For the above reaction, formation of Product A is favored by more than a 4:1 ratio over product B. Explain why. You may draw pictures of reaction intermediates to help justify your explanation.
Aromatic molecules that differ from benzene can also undergo EAS reaction. Shown below, is an example. CH3 NO₂+ CH3 CH3 N & d -NO₂ NO₂ B For the above reaction, formation of Product A is favored by more than a 4:1 ratio over product B. Explain why. You may draw pictures of reaction intermediates to help justify your explanation.
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Please include easy to follow explanations. I also attatched question 2 to provide context when it references a comparison to question 2

Transcribed Image Text:Aromatic molecules that differ from benzene can also undergo EAS reaction. Shown
below, is an example.
ہیں جات کی
N
CH3
N
CH3
-NO₂
B
N
CH3
For the above reaction, formation of Product A is favored by more than a 4:1 ratio over
product B. Explain why. You may draw pictures of reaction intermediates to help justify
your explanation.

Transcribed Image Text:For the reaction below, you are expecting similar results to those described in question
2. However, much more of the product D is observed in this reaction. Provide an
explanation for this change in selectivity as the starting substrate is modified.
CH3
H3C
z
N
-CH₂
NO₂+
CH3
H₂C
CH3
F
-NO₂
H₂C
D
N
CH3
NO₂
-CH3
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