The Ritter reaction is a useful method for producing substituted amides. Provide a detailed, arrow-pushing mechanism for the transformation. Show all reactive intermediates and all proton transfer steps. (It is not necessary to show every resonance structure for intermediates.)
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Q1: Draw a structure for these carboxylic acid
Q2: Rank the priority of principal groups in
Q3: Draw the major organic product of the
Q4: Provide a detailed, arrow-pushing mechanism for the
Q6: Choose the best reagent(s) for carrying out
Q7: Describe the equilibrium constant for the reaction.
Q8: Propose a synthesis of the transformation.
Q9: Which reagents could be used to synthesize
Q10: Predict the major organic product of the
Q11: Predict the major organic product of the
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