Chapter 19: Q18P (page 941)
What percent of imidazole is protonated at physiological pH (7.4)?
Short Answer
The percentage of imidazole protonated at physiological pH (7.4) is 20 %.
Chapter 19: Q18P (page 941)
What percent of imidazole is protonated at physiological pH (7.4)?
The percentage of imidazole protonated at physiological pH (7.4) is 20 %.
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Why is the conjugate acid of morpholine more acidic than the conjugate acid of piperidine?
Quinolines, heterocyclic compounds that contain a pyridine ring fused to a benzene ring, are commonly synthesized by a method known as the Skraup synthesis, in which aniline reacts with glycerol under acidic conditions. Nitrobenzene is added to the reaction mixture to serve as an oxidizing agent.
The first step in the synthesis is the dehydration of glycerol to propenal.
a. What product would be obtained if para-ethylaniline were used instead of aniline?
b. What product would be obtained if 3-hexen-2-one were used instead of glycerol?
c. What starting materials are needed for the synthesis of 2,7-diethyl-3-methylquinoline?
Question: Why is protonated pyrimidine ( pKa = 1.0 ) more acidic than protonated pyridine ( pKa = 5.2 ) ?
a.Draw the structure of 3-quinuclidinone.
b.What is the approximateof its conjugate acid?
c.Which has a lowervalue, the conjugate acid of 3-bromoquinuclidine or the conjugate acid of 3-chloroquinuclidine?
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