Chemistry, 24.04.2020 16:00 Tamiahufflululu
Primary amines can be prepared from nitriles by reduction with LiAlH4. The two-step sequence involves SN2 displacement of halide ion by cyanide ion followed by reduction, and yields a primary amine with one more carbon than was present in the alkyl halide. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions
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Primary amines can be prepared from nitriles by reduction with LiAlH4. The two-step sequence involve...
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