Please with the information provided how do I draw a balanced equation for the reactions by using acetic anhydride as the acylating agent and dicholomethane as the reaction solvent. of the 7-bonds of benzene toring and regenerate the catalyst (step 3). When the acyl group is acetyl (CH3as the acylating agent rather than acetyl chloride. The anhydride is safer to work with and it usually provbetter yields and a simpler work-up. More catalyst is needed with acetic anhydride however, because somthe aluminum chloride complexes with the acetic acid produced during the reaction, making it ineffectivecatalyst. As a rule, 2-3 moles of AlCl3 are used per mole of acetic anhydride.Step 1Step 2Step 3RH+CIR+AICI 3RRacylium ionR++ H+AICI4arenium ionAICI4Figure EAS.2: Mechanism of Friedel-Crafts acylationRAICI3 + HCI Friedel-Crafts Acylation ReactionDraw a balanced equation for the reaction. Include drawings of the structures of the reactant and all threepossible methoxyacetophenone isomers.

We know, Friedel Crafts Acylation reaction is an Electrophilic Aromatic Substitution Reaction. Here,…

Answered: Please with the information provided…

Please with the information provided how do I draw a balanced equation for the reactions by using acetic anhydride as the acylating agent and dicholomethane as the reaction solvent.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter16: Aldehydes And Ketones

Section: Chapter Questions

Problem 16.63P

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Concept explainers

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.

Question

Please with the information provided how do I draw a balanced equation for the reactions by using acetic anhydride as the acylating agent and dicholomethane as the reaction solvent.

of the 7-bonds of benzene to
ring and regenerate the catalyst (step 3). When the acyl group is acetyl (CH3
as the acylating agent rather than acetyl chloride. The anhydride is safer to work with and it usually prov
better yields and a simpler work-up. More catalyst is needed with acetic anhydride however, because som
the aluminum chloride complexes with the acetic acid produced during the reaction, making it ineffective
catalyst. As a rule, 2-3 moles of AlCl3 are used per mole of acetic anhydride.
Step 1
Step 2
Step 3
R
H
+
CI
R
+
AICI 3
R
R
acylium ion
R
+
+ H+
AICI4
arenium ion
AICI4
Figure EAS.2: Mechanism of Friedel-Crafts acylation
R
AICI3 + HCI

Friedel-Crafts Acylation Reaction
Draw a balanced equation for the reaction. Include drawings of the structures of the reactant and all three
possible methoxyacetophenone isomers.

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