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- propose synthesisWhy 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 a stepwise mechanism for the following reaction. Your mechanism must show how both organic products are formed.
- Draw a stepwise mechanism for the following reaction. This reaction combines two processes: the opening of an epoxide ring with a nucleophile and the addition of an electrophile to a carbon–carbon double bond. (Hint: Begin the mechanism by protonating the epoxide ring.)Draw the reaction and choose the correct characterizationsProblem 15 of 44 68 Draw the major product of this reaction. Ignore inorganic byproducts. TSOH, CH3CH2OH (2 equiv) Submit Assume that the water side product is continuously removed to drive the reaction toward products. Select to Draw