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1 vote
What is wrong with the following mechanism?

1) There is no leaving group, so there should be no arrows.
2) The arrow should be removing a proton from the H₂O group.
3) An arrow is also needed to indicate the loss of the leaving group.
4) The arrow indicating the formation of the C-Br bond (nucleophilic attack) should start at the bromide anion.

1 Answer

3 votes

Final answer:

The provided mechanism for a nucleophilic substitution reaction is incorrect due to several issues.

Step-by-step explanation:

The mechanism described in the question is for a nucleophilic substitution reaction. There are several issues with the mechanism:


  1. There is no leaving group indicated, which is necessary for a nucleophilic substitution reaction to occur.

  2. The arrow should be removing a proton from the H₂O group, not just pointing to it.

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

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

Overall, the provided mechanism does not accurately depict the steps and interactions involved in a nucleophilic substitution reaction.

User Vtni
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