Pyridine reacts with hydroxide by nucleophilic aromatic substitution. Complete the mechanism by drawing curved arrows, the structure of the charged intermediate, and the structure of the major uncharged product. All non-bonding electrons must be shown, including those associated with charges. Step 1: Draw curved arrows. Select Draw Templates More |||||||||CH| CIN 0 G () H | : 0: 50 Erase Q2Q Step 3: Draw the uncharged product. Chloride ion is pre-drawn for your convenience. Select Draw Templates More ||||||||| CHCIN O :a: Erase Step 2: Draw the charged intermediate. Draw curved arrows to form the product. Select Draw Templates More ||||||||||CH G V cl N O Erase Q2Q

Pyridine reacts with hydroxide by nucleophilic aromatic substitution. Complete the mechanism by drawing curved arrows, the structure of the charged intermediate, and the structure of the major uncharged product. All non-bonding electrons must be shown, including those associated with charges. Step 1: Draw curved arrows. Select Draw Templates More |||||||||CH| CIN 0 G () H | : 0: 50 Erase Q2Q Step 3: Draw the uncharged product. Chloride ion is pre-drawn for your convenience. Select Draw Templates More ||||||||| CHCIN O :a: Erase Step 2: Draw the charged intermediate. Draw curved arrows to form the product. Select Draw Templates More ||||||||||CH G V cl N O Erase Q2Q

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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