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psintusaichol psintusaichol
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Question 1.

What is wrong with the mechanism shown?




▸ An arrow is also needed to indicate the loss of the leaving group.

▸ There is no leaving group, so there should be no arrows.

▸ The arrow is backwards.

▸ The arrow should be removing a proton from the H2O group.

Question 2.

What is wrong with the mechanism shown?




▸ The arrow indicating the formation of the C-Br bond (nucleophilic attack) should start at the bromide anion.

▸ The arrow should be removing a proton from the H2O group.

▸ An arrow is also needed to indicate the loss of the leaving group.

▸ There is no leaving group, so there should be no arrows.
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Organic Chemistry

Organic Chemistry


Edition: 4th
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clubber25clubber25
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