Chapter 19: Q28P (page 946)
Pyrrole reacts with excess para-(N,N-dimethylamino)benzaldehyde to form a highly colored compound. Draw the structure of the colored compound.
Short Answer

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Chapter 19: Q28P (page 946)
Pyrrole reacts with excess para-(N,N-dimethylamino)benzaldehyde to form a highly colored compound. Draw the structure of the colored compound.

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Question:
a.Propose a mechanism for the following reaction:

b.What other product is formed in this reaction?
Benzene undergoes electrophilic aromatic substitution reactions with aziridines in the presence of a Lewis acid such as .
a. What are the major and minor products of the following reaction?
b. Would you expect epoxides to undergo similar reactions?

Rank the following compounds from strongest acid to weakest acid:

Propose a mechanism for the following reactions:


The chemical shifts of the C-2 hydrogen in the spectra of pyrrole, pyridine, and pyrrolidine are 2.82 ppm, 6.42 ppm, and 8.50 ppm. Match each heterocycle with its chemical shift.
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