Benzene reacts with ch3cocl in the presence of alcl3 to give
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AlCl3 is considered to be a Lewis Acid or in simpler words an “electron hungry species”. So, when it sees Acetyl Chloride (CH3COCl) it extracts the -Cl minus from the latter and itself gets transformed into AlCl4 minus. Now it is quite stable because his hunger has been satisfied.
Now it leaves behind an electrophile -COCH3 minus. We all know that benzene undergoes aromatic electrophilic substitution reactions. As a result the other electrophile gets attached to the benzene ring thereby forming Acetophenone (C6H5COCH3).
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hey mate here is your answer.....
When benzene reacts with ch3cocl in the presence of alcl3 Acetophenone(c6h5coch3) will form.This is a electrophilic substitution reaction. It is popularly named as as friedal Craft's acylation reaction.
hope it helps you....
When benzene reacts with ch3cocl in the presence of alcl3 Acetophenone(c6h5coch3) will form.This is a electrophilic substitution reaction. It is popularly named as as friedal Craft's acylation reaction.
hope it helps you....
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