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Heterocyclic aromatic compounds undergo electrophilic aromatic substitution in a similar fashion to that undergone by benzene with the formation of a resonance-stabilized intermediate. 3 2 Draw all of the resonance contributors expected when the above compound undergoes bromination at position 2

Heterocyclic aromatic compounds undergo electrophilic aromatic substitution in a similar fashion to that undergone by benzene with the formation of a resonance-stabilized intermediate. 3 2 Draw all of the resonance contributors expected when the above compound undergoes bromination at position 2

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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**Title: Resonance in Heterocyclic Aromatic Compounds** **Introduction:** Heterocyclic aromatic compounds undergo electrophilic aromatic substitution in a similar fashion to that undergone by benzene, forming a resonance-stabilized intermediate. **Task:** Draw all of the resonance contributors expected when the above compound undergoes bromination at position 2. **Instructions:** - Do not include lone pairs in your answer. They will not be considered in the grading. - Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. - Separate resonance structures using the ↔ symbol from the drop-down menu. **Diagram Tool:** The diagram tool shown is ChemDoodle®, which provides drawing and editing tools for chemical structures. You can utilize various shapes and bonds from the toolbar to create your structures. **Note:** Focus on illustrating the resonant forms accurately to reflect the stabilization in the intermediate during the bromination process at position 2.
Transcribed Image Text:**Title: Resonance in Heterocyclic Aromatic Compounds** **Introduction:** Heterocyclic aromatic compounds undergo electrophilic aromatic substitution in a similar fashion to that undergone by benzene, forming a resonance-stabilized intermediate. **Task:** Draw all of the resonance contributors expected when the above compound undergoes bromination at position 2. **Instructions:** - Do not include lone pairs in your answer. They will not be considered in the grading. - Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. - Separate resonance structures using the ↔ symbol from the drop-down menu. **Diagram Tool:** The diagram tool shown is ChemDoodle®, which provides drawing and editing tools for chemical structures. You can utilize various shapes and bonds from the toolbar to create your structures. **Note:** Focus on illustrating the resonant forms accurately to reflect the stabilization in the intermediate during the bromination process at position 2.
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