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- Draw the structure of the organic product of the following transformation. cat. ACOH NHWhy is it not advisable to use aqueous hydrochloric acid in a Grignard reaction of a ketone? A) The Grignard reagent will react with the acid and cannot react with the ketone. B) The ketone will be protonated and will become unreactive. C) The ketone will form an unreactive enol. D) The Grignard reagent won't dissolve in aqueous solutionsDraw out a complete arrow-pushing mechanism for the following reaction. This reaction is explicitly done with heat. O NaOH, H₂O heat
- Draw structures for the carbonyl electrophile and enolate nucleophile.Draw the products of the complete hydrolysis of an acetal. Draw all products of the reaction.What explains why many aldehydes and ketones can undergo self- condensation reactions in basic conditions? A. The alpha carbon can lose a proton and act like a nucleophile and the carbonyl carbon a an electrophile B. The alpha carbon can gain a proton and act like an electrophile and the carbonyl carbon is a nucleophile C. The oxygen of the carbonyl group can attack the carbon of the carbonyl group D. Only esters can undergo self-condensation reactions