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For each of the structures in parts (a) to (c) draw the outcome of the indicated electron movements.?

Answer 1

Sarah Angotti

Well for #a.# you got #C_6H_5C(-O^(-))=stackrel+NH_2#

And for #b.# you got enolate formation...

#C_5H_8O +H^(-) rarr C_5H_7O^(-) + H_2#

And for #c.# you make an hydrocarbyl radical...

#(H_3C)_3CH + dotBr rarr (H_3C)_3C* + HBr#

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Answer 2

Santiago Alfonso

Certainly! Please provide the specific structures in parts (a) to (c) along with the indicated electron movements, and I'll be happy to draw the outcomes for you.

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Answer from HIX Tutor

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.