Both pyridine and pyrrole are nitrogen- containing aromatic heterocyclic compounds (see below). When treated with HCI, pyridine forms a hydrochloride salt, whereas pyrrole is unreactive. Provide an explanation for this observed difference in reactivity. Pyridine (pK, 8.77) = Ĥ Pyrrole (pK, 17.8) = Select one: O A. The pyrrole nitrogen is a strongly deactivating group. B. Pyrrole has a large bond angle strain, preventing it from reacting. O C. Reaction of pyrrole with HCl forms an unstable nitrogenous anion.
Both pyridine and pyrrole are nitrogen- containing aromatic heterocyclic compounds (see below). When treated with HCI, pyridine forms a hydrochloride salt, whereas pyrrole is unreactive. Provide an explanation for this observed difference in reactivity. Pyridine (pK, 8.77) = Ĥ Pyrrole (pK, 17.8) = Select one: O A. The pyrrole nitrogen is a strongly deactivating group. B. Pyrrole has a large bond angle strain, preventing it from reacting. O C. Reaction of pyrrole with HCl forms an unstable nitrogenous anion.
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter23: Amines
Section: Chapter Questions
Problem 23.72P
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