Draw the product the the adhering to reaction in between propanoylchloride and also p-methoxynitrobenzene. Include formal charges.

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Friedel handmade acylation reaction is one electrophilic substitution reaction on aromatic rings, wherein the acyl cation acts together an electrophile in the process. This reaction procedure is catalyzed by a Lewis acid.


General friedal handmade acylation reaction

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Acylation reaction proceeds through 3 steps

1.Generation of electrophile indigenous the acyl chloride

2.Electrophile substitution top top aryl ring

3.Transfer the proton to gain back aromaticity


1.Generation the electrophile from the acyl chloride

The provided acyl chloride is propionyl chloride

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An electrophile has actually been produced from the Lewis acid and the provided acyl chloride. The Lewis acid abstracts the chloride ion from the acyl chloride and gives an acyl cation as well as a AlCl4\u2212\\rmAlC\\rml_\\rm4^ - AlCl4\u200b\u2212complex.


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2.Electrophile substitution ~ above aryl ring

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3.Transfer of proton to attain aromiticity

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The complete reaction is

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An electrophile is substituted at the carbon place where the high electron density is located on the ring. Then, the aromatization procedure takes place to attain stability in the ring. Aromatization takes place through the deliver of nearby protons to the ring. The proton is climate abstracted by the halide ion, forms HCl\\rmHClHCl and a Lewis acid.

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