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Rank imidazole, pyrrole, and benzene from most reactive to least reactive toward electrophilic aromatic substitution.
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Rank imidazole, pyrrole, and benzene from most reactive to least reactive toward electrophilic aromatic substitution.
Why is imidazole a stronger acid (pKa ~ 14.4) than pyrrole (pKa ~ 17)?
Imidazole boils at 257 °C, whereas N-methylimidazole boils at 199 °C. Explain the difference in boiling points.
What are the products of the following reactions?
b.
What are the products of the following reactions?
a.
Why is protonated pyrimidine (pKa = 1.0) more acidic than protonated pyridine (pKa = 5.2)?