Chemistry Asked on January 9, 2021
In this reaction, why does $ce{MgBr}$ goes to the $ce{>NH}$ group and form a bond with nitrogen by removing $ce{-H}$.
Also where does the negative charge go?
There is no step 1 and step 2 in this reaction. Both are consecutive and second one is fast because it is an acid-base reaction:
Note that approximate $mathrm{p}K_mathrm{a}$ values of ring $ce{C-H}$ and $ce{N-H}$ are 50 and 40, respectively. Thus, as soon as Grignard reagent is formed, it exchanges relatively acidic protons of $ce{N-H}$ fast (Remember, Grignard is also a strong base). To visualize the exchange process, I included schematic representation at the bottom of the image.
Correct answer by Mathew Mahindaratne on January 9, 2021
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