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Author Question: Both pyridine and pyrrole are nitrogen containing aromatic heterocyclic compounds. When treated with ... (Read 36 times)

llesku

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on: Feb 17, 2022
Both pyridine and pyrrole are nitrogen containing aromatic heterocyclic compounds. When treated with HCl, only pyridine forms a hydrochloride salt, whereas pyrrole is unreactive. Which of the following is not a valid explanation for this observed reactivity?



◦ The lone pair on pyridine can be protonated without disrupting the aromatic stability.
◦ The lone pair on pyrrole is involved in making the compound aromatic and thus is less susceptible to protonation.
◦ The lone pair on pyridine is not part of the aromatic system.
◦ The lone pair on pyrrole is sp3 hybridized and is less prone to protonation.
◦ Protonation of pyrrole leads to a nonaromatic cation, which is less stable.
Organic Chemistry ¦ Klein ¦ 4th Edition
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Marked as best answer by llesku on Feb 17, 2022

LynellDool

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Reply #1 on: Feb 17, 2022
Lorsum iprem. Lorsus sur ipci. Lorsem sur iprem. Lorsum sur ipdi, lorsem sur ipci. Lorsum sur iprium, valum sur ipci et, vala sur ipci. Lorsem sur ipci, lorsa sur iprem. Valus sur ipdi. Lorsus sur iprium nunc, valem sur iprium. Valem sur ipdi. Lorsa sur iprium. Lorsum sur iprium. Valem sur ipdi. Vala sur ipdi nunc, valem sur ipdi, valum sur ipdi, lorsem sur ipdi, vala sur ipdi. Valem sur iprem nunc, lorsa sur iprium. Valum sur ipdi et, lorsus sur ipci. Valem sur iprem. Valem sur ipci. Lorsa sur iprium. Lorsem sur ipci, valus sur iprem. Lorsem sur iprem nunc, valus sur iprium.
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llesku

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Reply 2 on: Feb 17, 2022
Thanks for the timely response, appreciate it

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