Reaction of toluene at high temperatures gives us (o-m)toluene; whereas at normal conditions of electrophilic attack, it gives us (o-p) directing.
Why does this happen at high temp although as methyl group is activating and o-p directing?
Reaction of toluene at high temperatures gives us (o-m)toluene; whereas at normal conditions of electrophilic attack, it gives us (o-p) directing.
Why does this happen at high temp although as methyl group is activating and o-p directing?
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