Question

Question: How is it possible for H2OCl+ to be the active oxidizing agent? Why wouldnt the answer be:

NaOCl + CH3COOH ---> HOCL + CH3COONa?

How is it possible for HOCL to accept another electron?

THE CORRECT ANSWER IS LABLED BELOW:

Meta is the least stae intermediate here, but then ortho becomes least stable products. Why is this? Products also are given.

Products:

он 5.25 % NaOCl Acetone, CH&COOH 9-fluorenone 9-fluorenol c) Provide the balanced chemical equation that accounts for the production of the active oxidizing agent. (2 pts) わ [Nal tOCi] + CH3COOH [CH3COO) INalHOCI HOCI + CH3COOH [CH3COO] [H20CII Bold active oxidizing agent Anisole can react with propionyl chloride in the presence of a Lewis acid catalyst in an electrophilic aromatic substitution to produce one or more anisole derivatives. (18 pts total) CI FeCls. CH2Cl2 a) The regiochemical outcome of the reaction is governed by the kinetic favorability of one reaction pathway over another. Draw a potential energy surface showing the formation of the possible regioisomeric arenium intermediates from the starting material. For the arenium intermediate on the lowest-energy pathway, justify its stability relative to the other arenium cation intermediates. (8 pts total) I WM ome Cl ortho meto a:

Answer 1

5.1s . Naod one, cn,Coo hoc alcsha chleroos cad poshal Io digso cickes iato the anion Fe ㄋ