Both pyrrole and pyridine are aromatic compounds, and undergo electrophilic aromatic substitution (EAS). Using a resonance argum
ent, predict the regiochemistry of EAS on both pyrrole and pyridine. As part of your argument, you must draw resonance structures for the arenium ion leading to each possible regiochemistry, and compare the stabilities of the resonance hybrids. In addition, make a reasoned statement about whether you think each one would react faster or slower than benzene and why.
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Its main advantage is <em>they information fits on one line of text</em> <u>(thus works well when using the formula in paragraphs)</u>. Disadvantages are <em>they can be confusing for larger molecules</em>
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hope this helps :3
