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).

< > according to newton's third law of motion, forces always act in equal but opposite pairs. another way of saying this is for every action, there is an equal but opposite reaction.< >