4:31 41. (6pts) The following compound, the conjugate acid of pyridine, undergoeselectrophilic aromatic substitution preferentially at the 3 position as illustrated by thesynthesis of 3-nitropyridine below.+ HNO,Expert Q&AH₂SO4+ H₂ODoneOffer a detailed explanation (using relevant structures) for the preferential nitration at the3 position (remember to compare to other possible products!).

In the question a reaction is given with the product and it is asked to explain the reason behind…

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

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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