Enamines can act as carbon nucleophiles and react with acyl chlorides. Draw any non-bonding electrons or charges on the structure of the enamine provided below, then using curved arrows provide a step by step mechanism showing any intermediates along the reaction pathway for the acylation reaction with benzoyl chloride to yield the product. C IL. -t.. - £.ll manl enamine

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Enamines can act as carbon nucleophiles and react with acyl chlorides. Draw any non-bonding electrons or
cnarges on the structure of the enamine provided below, then using curved arrows provide a step by step mechanism
showing any intermediates along the reaction pathway for the acylation reaction with benzoyl chloride to yield the
product. C
-t.. f..Jl mal.-
enamine
Transcribed Image Text:Enamines can act as carbon nucleophiles and react with acyl chlorides. Draw any non-bonding electrons or cnarges on the structure of the enamine provided below, then using curved arrows provide a step by step mechanism showing any intermediates along the reaction pathway for the acylation reaction with benzoyl chloride to yield the product. C -t.. f..Jl mal.- enamine
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