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

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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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
Transcribed Image Text: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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