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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Get started for freeWhy is imidazole a stronger acid (pKa = 14.4) than pyrrole (pKa~ 17)?
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?
Rank the following compounds from easiest to hardest at removing a proton from its methyl substituent:
Organic chemists work with tetraphenylporphyrins rather than with porphyrins because tetraphenylporphyrins are much more resistant to air oxidation. Tetraphenylporphyrin can be prepared by the reaction of benzaldehyde with pyrrole. Propose a mechanism for the formation of the ring system shown here:
What is the major product of the following reactions?
(a)
(b)
(c)
(d)
(e)
(f)
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