Give the structures of the substitution products expected when 1-bromohexane reacts with: part a naoch2ch3
1 answer:
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.
<span>The substitution product formed will be 1-ethoxybutane (main product) and sodium bromide (side product).</span>
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The Lewis structure of Diimide (N₂H₂) is shown below.
In this molecule two Nitrogen atoms attached to each other through a double bond are further attached to one one Hydrogen atom. Also, each Nitrogen atom carries one non-binding electron pair (Lone Pair) (Highlighted RED).
Result:
Option-C (<span>each nitrogen has one nonbinding electron pair) is the correct answer.</span>
In this molecule two Nitrogen atoms attached to each other through a double bond are further attached to one one Hydrogen atom. Also, each Nitrogen atom carries one non-binding electron pair (Lone Pair) (Highlighted RED).
Result:
Option-C (<span>each nitrogen has one nonbinding electron pair) is the correct answer.</span>