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- It is not necessary for a nucleophile to have an unshared electron pair. O True O False2) Use your understanding of reaction rates to identify the faster reaction for each of the following pairings. HC Br O CECH Br 2 equiv of OR H NH2 Br 2 equiv of ONH2 BrPlease predict the product of the given reactant to complete the reaction. Indicate NR if there is no reaction.
- 2. For each of the following pair of reactions, CIRCLE the reaction that will occur faster (A or B). A A A H. 1 Br Br CH3ONa CH3OH NaCN ACN Nal DMSO B B B |||||| Br CI Br CH3ONa CH3OH NaCN ACN Nal DMSOFor the following reactions, explain which product(s) will form and why. Cro; H2SO4 PCC Cro3 HO H2SO4Draw an energy diagram of the following reactions. A one step reaction with a positive AG A one step reaction with a negative AG A two-step reaction with an overall positivel-Where the intermediates are lower energy than the reactants and the first transition state is lower in energy than the second.
- 027 In Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 4 See Periodic Table O See Hint :0: :Br: Add the missing curved arrow notation. S CI Br Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Kea > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e., Keq« 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg 1) because bromide is a better leaving group than acetate. +which reagents/mechanism complete this reaction? Solve plzzz!!!.Draw ALL possible products that could result given the following reaction. H&C H₂O