- #1
crays
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Hi, my teacher told me that the oxygen in phenol would be delocalized into the benzene ring's electron and thus, making the O-H bond weaker, thus easing the release of the H proton. But i would like to know, since a benzene consist of 3 double bonds, shouldn't the electrons from the benzene itself already occupied most of the shield, thus making it harder for any other electrons to be joined in? Wouldn't the Oxygen, O's electron be repel if they try to merge into the benzene's electron cloud?