Using resonance structures, show why the amino group is activating. Consider an attack by the electrophile E1 at the para position.
a. For the substituent in this experiment that was found to be least activating, explain why bromination took place at the position on the ring indicated by the experimental results.
b. What other experimental techniques (including spectroscopy) might be used to identify the products in this experiment?
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Using resonance structures, show why the amino group is activating. Consider an attack by the electr...
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