Give the structures of the substitution products expected when 1-bromohexane reacts with: part a naoch2ch3

Actually since Bromine is located at the 1 Carbon, so we can say that this is a primary alkyl halide and which undergoes SN2 or E2 reactions. This reaction is a bimolecular, single step process because it is a primary.

The substitution product formed will be 1-ethoxybutane (main product) and sodium bromide (side product).

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