thiophene imidazole 2. The NH in imidazole (pKa-18) is more acidic than normal alkyl-substituted amines (pKa-30-35) (such as diethylamine). What makes functional groups acidic in organic chemistry? Please rationalize the acidity of imidazole with a couple short sentences and a detailed figure that supports your explanation. 3. If your product from this experiment (benrimidazole) in

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Chapter1: Chemical Foundations
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start with thiophene).
thiophene
imidazole
2. The NH in imidazole (pKa=18) is more acidic than normal alkyl-substituted amines (pKa-30-35) (such
as diethylamine). What makes functional groups acidic in organic chemistry? Please rationalize the
acidity of imidazole with a couple short sentences and a detailed figure that supports your explanation.
3. If your product from this exneriment (henzimidazole
Transcribed Image Text:start with thiophene). thiophene imidazole 2. The NH in imidazole (pKa=18) is more acidic than normal alkyl-substituted amines (pKa-30-35) (such as diethylamine). What makes functional groups acidic in organic chemistry? Please rationalize the acidity of imidazole with a couple short sentences and a detailed figure that supports your explanation. 3. If your product from this exneriment (henzimidazole
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