Predict the major product from the treatment of (trifluoromethyl)benzene with acetyl chloride and aluminium(III) chloride. Draw the full mechanism for the reaction, using appropriate arrows to indicate electron movement and the full structures (i.e resonance forms) of any intermediate(s). Your current response is: F3C CI AICI 3 Click here to open the canvas Use the mechanism of the reaction to provide a rationale for why the major product formed. ChemDoodle

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