The reaction is friedel craft acyalation.
Lets show the mechanism. :
Step1) AlCl3 is lewis acid and it abstract the electron pairs on Cl
step 2)
Step 3) Attack of pie electrons of benzene :
step 4) Abstracton of H by Cl-
Now product formed by reacting with Cl2 in presence of FeCl3
The CH3CO group is ortho para directing and to avoid steric hinderance Cl goes to para postion.
Lets the show the mechanism.
step 2
Q 2 )
This reaction is friedel craft alkylation:
We show the mechanism
Primary carbocation formed is unstable so by rearrangement it forms secondary
Attack of benzene
2. Draw the major product or products of the following electrophilic aromatic substitutionreactions. Assume each substitution...
Am I on the right track? Please help! Draw the major product or products of the following electrophilic aromatic substitution reactions. Assume each substitution occurs only once.
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