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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 BrFor the following reactions, explain which product(s) will form and why. Cro; H2SO4 PCC Cro3 HO H2SO4
- Please predict the product of the given reactant to complete the reaction. Indicate NR if there is no reaction.Draw 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.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 DMSO
- Hi can someone please help me by explaining the reaction mechanism of this reaction please? Thank you027 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. +Drawing Reaction Mechanism Arrows