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Reaction Scheme: y NO ON-OH oso3H -ÕH₂ HSO4 8 O=NO Betu H- HSO4 OCH3 O₂N nitronium OCH3 OCH3

Reaction Scheme: y NO ON-OH oso3H -ÕH₂ HSO4 8 O=NO Betu H- HSO4 OCH3 O₂N nitronium OCH3 OCH3

Chemistry
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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Nitrating methyl benzoate. 1.Describe the mechanism of EAS clearly and in detail 2. What is the effect of subtituent of the outcome of EAS；include 3 classes of subtituents
Reaction Scheme: ON-OH NO HOSO3H -ÕH₂ HSO4 8 O=NO Bete H- HSO4 OCH3 O₂N nitronium OCH3 OCH3
Transcribed Image Text:Reaction Scheme: ON-OH NO HOSO3H -ÕH₂ HSO4 8 O=NO Bete H- HSO4 OCH3 O₂N nitronium OCH3 OCH3
CH3O + No m² Least stable CH3R P- + CH30 •NO ₂ schoo NO2 NO2 CHOREO CH300 NO2 NO- Least Stable _NO₂ + lley College NO₂ CHO 102 Why Meta position is most stable form Electrophilic attack at either the ortho- or para-position positive charge on the carbon that bears places a the substituent ((+30=0). n A
Transcribed Image Text:CH3O + No m² Least stable CH3R P- + CH30 •NO ₂ schoo NO2 NO2 CHOREO CH300 NO2 NO- Least Stable _NO₂ + lley College NO₂ CHO 102 Why Meta position is most stable form Electrophilic attack at either the ortho- or para-position positive charge on the carbon that bears places a the substituent ((+30=0). n A
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