2C. Write the separation scheme for the isolation of 4-methyl acetophenone from the reaction mixture in the experiment provided.

Organic Chemistry
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ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter3: Organic Compounds: Alkanes And Their Stereochemistry
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ANSWER 2C

NOTE: THIS CAN NOT BE HAND-DRAWN OR WRITTEN. EXPLANATION MUST BE DIGITALLY ILLUSTRATED/TYPED!

2A. What is the theoretical yield and limiting reagent for the Friedel Crafts acylation reaction of toluene
as described in the experiment provided if the reaction is started with 5 g of aluminum chloride, 25 mL
of dichloromethane (total), 3.5 g acetyl chloride, and 3.7 mL of toluene?
2B. What are the safety precautions used in the experimental procedure provided to prevent exposure
to HCI gas?
2C. Write the separation scheme for the isolation of 4-methyl acetophenone from the reaction mixture
in the experiment provided.
Transcribed Image Text:2A. What is the theoretical yield and limiting reagent for the Friedel Crafts acylation reaction of toluene as described in the experiment provided if the reaction is started with 5 g of aluminum chloride, 25 mL of dichloromethane (total), 3.5 g acetyl chloride, and 3.7 mL of toluene? 2B. What are the safety precautions used in the experimental procedure provided to prevent exposure to HCI gas? 2C. Write the separation scheme for the isolation of 4-methyl acetophenone from the reaction mixture in the experiment provided.
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