O COOH (1) SOCI₂ (2) AlCl3

Chemistry
10th Edition
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
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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What would be the product of this reaction? What are the exact arrows/mechanism?

I know the first part, where an acyl chloride is synthesized but I have no idea how to do acylation with the given reagents. 

The image depicts a chemical reaction scheme. On the left side is the structural formula of a benzoic acid derivative with a propyl chain attached to the benzene ring. The molecular formula of the compound is C₉H₁₀O₂ or C₆H₅(CH₂)₃COOH.

To the right, there is an arrow indicating a reaction sequence. Above the arrow, the text "(1) SOCl₂" is written, indicating the first step involving thionyl chloride. Below the arrow, the text "(2) AlCl₃" is written, indicating the second step involving aluminum chloride.

This reaction likely represents the conversion of a carboxylic acid into an acyl chloride using thionyl chloride, followed by a Friedel-Crafts acylation reaction using aluminum chloride as a catalyst.
Transcribed Image Text:The image depicts a chemical reaction scheme. On the left side is the structural formula of a benzoic acid derivative with a propyl chain attached to the benzene ring. The molecular formula of the compound is C₉H₁₀O₂ or C₆H₅(CH₂)₃COOH. To the right, there is an arrow indicating a reaction sequence. Above the arrow, the text "(1) SOCl₂" is written, indicating the first step involving thionyl chloride. Below the arrow, the text "(2) AlCl₃" is written, indicating the second step involving aluminum chloride. This reaction likely represents the conversion of a carboxylic acid into an acyl chloride using thionyl chloride, followed by a Friedel-Crafts acylation reaction using aluminum chloride as a catalyst.
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