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- What will happen if a carboxylic acid reacts with a Grignard reagent? Draw and explain the mechanism.Draw the major organic product for the following two-step reaction.Identify the electrophile and the nucleophile in each of the following reaction steps. Then draw curved arrows to illustrate the bond-making and bond-breaking processes.
- Draw the major organic product or products for the reaction. Multiple products may be drawn in one box, in any order. Include charges as needed. .F HNO3, H2SO4 F.complete the following synthesis produces using a proper reagent and productsExplain why quinuclidine is a much more reactive nucleophile than triethylamine, even though both compounds have N atoms surrounded by three R groups.
- Which reaction intermediate (A or B) is more likely to form in the epoxide ring opening reaction? Reactions prefer to react through lower energy intermediates. Hint: how might you justify one structure being lower in energy than the other? Draw structures as part of your explanation why. F F. BOH F :0. Br Br Br H H epoxide ring opening Structure A Which alcohol structure shown below would be less acidic? Explain why. OH Structure B : 0. : OHDraw the two resonance structures of the enolate anion intermediate for this reaction.draw the mechanism for the following williamson ether synthesis.
- what's the reagent? ( explain well with step by Step Answer. ).Which reaction intermediate (A or B) is more likely to form in the epoxide ring opening reaction? Reactions prefer to react through lower energy intermediates. Hint: how might you justify one structure being lower in energy than the other? Draw structures as part of your explanation why. Structure A Structure B ерoxide ring opening HO, : ОН Which alcohol structure shown below would be less acidic? Explain why. F F. Br Br Brwe are only allowed to use a one carbon aldehyde. in the step after the wiitig reacation. i am sorry i should have mentioned before