The reaction between propionyl chloride and acetate ion is outlined below. a) Complete the mechanism of the forward reaction by placing curved arrows to show the electron movements in the reactants and intermediate product. i: :0: b) Draw the structures of the final product and leaving group, including any charges. (Electrons may be omitted.) 1L
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- The question is: "Draw the curved arrow mechanism for the reaction between pentan-2-one and (CH3)3O– in t-butanol to form an enolate. Draw all electrons and charges on both resonance structures. Then answer the question about the reaction." I got the initial arrows correct, but am not entirely sure what the carbanion intermediate would look like and then what the curved arrows would be to convert it to its final oxanion formDraw a stepwise mechanism for enol forming reaction shown below. You must show the structures of all intermediates and indicate electron flow with curly arrows.Draw the FULL electron-pushing mechanism for the reaction to synthesise Lidocaine, including ALL intermediates (with formal charges) and electron pushing arrows. label the electrophile and nucleophile in each step!
- A. Write appropriate reagents over the reaction arrow B. As a result of this reaction, is the N made more nucleophilic or less nucleophilic?Draw a detailed step-wise mechanism for the following reactions. Be sure to show all steps, formal charges, and show the movement of electrons with curved arrows.The following molecule is an intermediate in the sythesis of strychnine, a poison commonly used as a rodenticide. The intermediate has a free alkoxide group, which serves as a nucleophile. Which site is electrophilic and in close enough proximity to be attacked by this nucleophile?
- Draw a complete stepwise mechanism for the acid-catalyzed hydration of the alkene shown below. You must show the structures of all intermediates and indicate electron flow with curly arrows.1. For the following reaction step, indicate which pattern of arrow pushing it represents. a. proton transferb. rearrangementc. loss of a leaving group2. Melphalan, a drug used in chemotherapy, reacts with itself in the body before binding with its target, as illustrated in the mechanism below. What is the first pattern of arrow pushing seen in this reaction? a. rearrangementb. loss of a leaving groupc. nucleophilic attackDetermine if CH3CH2ONa is a suitable reagent to deprotonate the following compound. Explain why. Draw the complete reaction, including the curved arrow mechanism.
- Draw the curved arrow(s) to depict the formation of the keto form of an enolate ion via a strong base, B. Complete the resonance structures of the enolate anion\'s keto and enolate forms with bonds, charges, and nonbonding electron pairs. Use curved arrows to show how the keto form resonates to the enolate form.When the depicted alkyne is treated first with sodium amide and then with the alkyl halide shown, one of the depicted products is formed Circle the correct product and write the steps in the mechanism that show how this reaction occurs to form the product you selected. Add the following A. all necessary curved arrows B. the structure of any intermediates that are formed during the mechanism, including stereochemistry C, what, if anything, is added or lost during each step of the mechanism, D any nonzero formal charges. Only use materials those that are given in the equation.Identify the electrophile and the nucleophile in each of the following reaction steps and then draw curved arrows to illustrate the bond-making and bondbreaking processes.