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- ton Draw the mechanism for each reaction ་ 1. он MAJ 2. Ugot 1.-04 2. H₂0 HO Nu HO OH HO 244 S Explain why these reactions produce different products. Reference mechanisms in in your answer. your3. The following three SNAR transformations follow different mechanisms. Draw an intermediate or transition state for each reaction that relates the correct mechanism. Write a short sentence as to why that is the correct intermediate for the reaction. Reaction 1: Reaction 2: NO2 NO2 NO₂ + NaOMe NO2 + NaOH2 1. aq NaHCO3. 100 C 2. H₂O+ OMe NO2 NO₂ OH ŇO₂ NO2 Reaction 3: CFa Br CF3 8--2 + NaNH2 NH3 NH₂ Intermediate/transition state Intermediate/transition state Intermediate/transition stateSECTION 6: Show the mechanism of each reactions with arrows and intermediates form as in a. b. C. HBr Br₂ Cl₂, H₂O Br Br CI Br OH
- 2. Identify the common intermediate in the box. State what the mechanism is for the intermediate to the product (S.1, S 2, E1, or E2) N Br ||||| tBuOK tBuOH tBuOK tBuOH3) Explain why the reactions below proceed at different rates and have different product OTS OTS KOtBu slow KOtBu fast andPlease provide mechanism and structures for intermediate A and intermediate B
- The correct answer is D, can you please draw the mechanism for the set of reactions shown? A. 1. H,O* 2. PBГ3 3. TMSCI, Et,N 4. Mg, Et,0 5. В. 1. HBr 2. Mg, Et,0 3. 4. Cro3, pyridine (excess) 6. Cro3, pyridine (excess) С. 1. HBr 2. TMSCI, Et,N 3. Mg, Et,0 o D. 1. HBr 2. TMSCI, Et,N 3. Mg, Et,0 4. 4. OMe 5. TBAF 6. CrO3, pyridine (excess) 5. TBAF 6. CrO3, pyridine (excess)draw the mechanism4. Please choose either Reaction A or Reaction B, and then provide the complete mechanism. The mechanism MUST include the formation of the "super electrophile." Then provide the reaction coordinate pathway starting from benzene + super electrophile. Be sure to include an energy access and labels for reactants, products, intermediates, energies of activation, and transition states. Reaction A NO2 Reaction B HNO3, H2SO4 CH3COCI, AICI3