Asked by Tony
Draw and describe the three overall redox reactions than occur in the conversion
of 2,6-dimethylnitrobenzene to 2,6-dimethylaniline using stannous chloride. (Not
the mechanisms). What are the key structures in these reactions, and what are their
oxidation states? What are the reducing and oxidizing agents?
Now I got the overall mechanism that I figured out but I'm having problems calculating the redox reactions. Can anyone help?
of 2,6-dimethylnitrobenzene to 2,6-dimethylaniline using stannous chloride. (Not
the mechanisms). What are the key structures in these reactions, and what are their
oxidation states? What are the reducing and oxidizing agents?
Now I got the overall mechanism that I figured out but I'm having problems calculating the redox reactions. Can anyone help?