The formation of an azo compound is a slow reaction, but that rate can be increased by raising the pH of the solution. Why is this necessary? In other words, how does the pH of the solution affect the reactivity of the N,N-dimethylaniline reagent.© BrainMass Inc. brainmass.com October 16, 2018, 4:30 pm ad1c9bdddf
The solution is given as a succinct explanation.
Synthesis And Reaction Problems with Amines
Please see the attached file.
1. Write the complete stepwise mechanism for the reaction below. Show all intermediate structures and all electron flow arrows.
2. Give the major organic product(s) of each of the following reactions or sequences
of reactions. Show all relevant stereochemistry.
3. Classify the following nitrogen atoms in the following compounds as primary, secondary, tertiary, or quaternary.
this reaction is an example of
a. a hofmann rearrangement
b. a Gabriel synthesis
c. a hofmann elimination reaction
d. a curtius rearrangement
5. Name the following compounds by IUPAC rules:
6. From the list, choose the best reagent(s) for each step in the following synthesis. There is only one answer for each reaction
7. The strork enamine reaction is a variation on the Michael reaction which utilizes an enamine nucleophile.
Draw the structures of the Ketone + Amine products of this reaction.View Full Posting Details