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18 Nov 2019
A classic method for forming primary amines is using an imide with the three-step process highlighted below: (imide = two amides connected by a common nitrogen) A. Propose a mechanism for the reaction above. You must show correct arrows, relevant lone pairs, bonds, and formal charges to get full credit. The major resonance structure of any resonance-stabilized intermediate must be drawn and labelled "major". B. This method is does not work for secondary halides because of a significant side reaction. Identify this side reaction and show the product that is formed from it.
A classic method for forming primary amines is using an imide with the three-step process highlighted below: (imide = two amides connected by a common nitrogen) A. Propose a mechanism for the reaction above. You must show correct arrows, relevant lone pairs, bonds, and formal charges to get full credit. The major resonance structure of any resonance-stabilized intermediate must be drawn and labelled "major". B. This method is does not work for secondary halides because of a significant side reaction. Identify this side reaction and show the product that is formed from it.