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When phenyl 3,4-dimethylbenzoate undergoes electrophilic aromatic substitution, one ring reacts much more readily than t

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When phenyl 3,4-dimethylbenzoate undergoes electrophilic aromatic substitution, one ring reacts much more readily than t

Posted: Wed Dec 15, 2021 10:46 am
by answerhappygod
When Phenyl 3 4 Dimethylbenzoate Undergoes Electrophilic Aromatic Substitution One Ring Reacts Much More Readily Than T 1
When Phenyl 3 4 Dimethylbenzoate Undergoes Electrophilic Aromatic Substitution One Ring Reacts Much More Readily Than T 1 (23.43 KiB) Viewed 94 times
When phenyl 3,4-dimethylbenzoate undergoes electrophilic aromatic substitution, one ring reacts much more readily than the other. (a) Which one is it? Encircle the ring (b) Explain your answer. (c) Draw the resulting product/s when it undergoes bromination reaction. (10 pts)
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