Please help with both questions ?!CH3COCIAICI 3H3CAromatic rings can be acylated to yield ketones by treatment with AlCl3 and an acid chloride. The reactive species is an electrophilic, resonance-stabilized acylium ion.Draw curved arrows to show the movement of electrons in this step of the mechanism.Arrow-pushing InstructionsXIلىAICI 3CH3H3C-C=0AICI4 Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the cyano with the ortho positionin benzonitrile.OCENbenzonitrile• You do not have to consider stereochemistry.• Include all valence lone pairs in your answer.• In cases where there is more than one answer, just draw one.?

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Arrow-pushing Instructions NA Aromatic rings can be acylated to yield ketones by treatment with AlCl3 and an acid chloride. The reactive species is an electrophilic, resonance-stabilized acylium ion. Draw curved arrows to show the movement of electrons in this step of the mechanism. H3C CH3COCI AICI3 XT CI CH3 AICI 3 H3C-C=0 AICI4

Arrow-pushing Instructions NA Aromatic rings can be acylated to yield ketones by treatment with AlCl3 and an acid chloride. The reactive species is an electrophilic, resonance-stabilized acylium ion. Draw curved arrows to show the movement of electrons in this step of the mechanism. H3C CH3COCI AICI3 XT CI CH3 AICI 3 H3C-C=0 AICI4

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 19E

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