k on the electrophile in each pair of reactants (one from top pair and from bottom pair): Targets placed: 1/2 u can place up to 2 targets O NH HO .F Undo Delete selected Remove All
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- 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 See Periodic Table O See Hint :ö: :Br: Add the missing curved arrow notation. 20 F CI Br I 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., Keg > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e. Keg « 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.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. +Of the following, which is the best electrophile? i Ph. HO OEt NH₂
- 7. Draw the mechanism for the reaction. There should be three steps: 1) protonation, 2) Nu attack, 3) proton removal. -ОН H* НоConsider the E1 reaction of the tertiary halide shown. Н. :Br: : ОН H :Br: + NaOH -H- product Step 1: Add curved arrow(s). Step 2: Add curved arrow(s). Select Draw Rings More Erase Select Draw Rings More Erase C H Br C H Br : Br : H : Br H H 'o:Draw the organic product of the nucleophilic substitution reaction. Include all hydrogens atoms. CH³CH₂I + CH³CH₂O¯ Select Draw с Rings O H I More + Erase D
- Please answer 8, 13 & 17 Correct answers are circled. Please explain the mechanismsWhich compound is most nucleophilic? * О Option 5 О снзSH CH3SH О снзон О снзсо2н CH3CO2H О 120 Н2029) Draw all of the expected products for the following reaction. Circle the most dominant product in each reaction. 'BUOK 3 NaOEt
- Will the following bases favor an E1 or E2 mechanism? Sort them into the appropriate boxes below. 1st attempt See Periodic T Bases (6 items) (Drag and drop into the appropriate area below) H20 "NH2 CH3CH2OH NaH tBuo CH3CO2 Favored Reaction El Favored E2 Favored O OF 20 QUESTIONS COMPLETEDMost nucleophilic 3860 Br CI F Least nucleophilic Answer BankExplain why furan is primary substituted at the 2 positive when it undergoes reaction. E* E an EAS