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1. (6pts) The following compound, the conjugate acid of pyridine, undergoes electrophilic aromatic substitution preferentially at the 3 position as illustrated by the synthesis of 3-nitropyridine below. NO₂ H +HNO, H₂SO4 Offer a detailed explanation (using relevant structures) for the preferential nitration at the 3 position (remember to compare to other possible products!). + H₂O

1. (6pts) The following compound, the conjugate acid of pyridine, undergoes electrophilic aromatic substitution preferentially at the 3 position as illustrated by the synthesis of 3-nitropyridine below. NO₂ H +HNO, H₂SO4 Offer a detailed explanation (using relevant structures) for the preferential nitration at the 3 position (remember to compare to other possible products!). + H₂O

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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4:31 4 1. (6pts) The following compound, the conjugate acid of pyridine, undergoes electrophilic aromatic substitution preferentially at the 3 position as illustrated by the synthesis of 3-nitropyridine below. + HNO, Expert Q&A H₂SO4 + H₂O Done Offer a detailed explanation (using relevant structures) for the preferential nitration at the 3 position (remember to compare to other possible products!).
Transcribed Image Text:4:31 4 1. (6pts) The following compound, the conjugate acid of pyridine, undergoes electrophilic aromatic substitution preferentially at the 3 position as illustrated by the synthesis of 3-nitropyridine below. + HNO, Expert Q&A H₂SO4 + H₂O Done Offer a detailed explanation (using relevant structures) for the preferential nitration at the 3 position (remember to compare to other possible products!).
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