The reaction would be slower because bromide is a poorer leaving group. The reaction would be faster because bromide is a better leaving group. No change in the rate of the reaction would be observed because it does not depend on the nature of the halogen. The reaction would be faster because the C-Br bond is weaker than the C-CI bond. The reaction would be slower because the C-Cl bond is weaker than the C-Br bond.

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Chapter1: Chemical Foundations
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A student uses a bromoacetic acid instead of a-cloroacetic acid for the Williamson Ether Synthesis reaction. which statements below are correct? (choose all that apply)

A student uses a-bromoacetic acid instead of a-chloroacetic acid for the reaction. Which statements below
are correct? (Check all that apply)
The reaction would be slower because bromide is a poorer leaving group.
O The reaction would be faster because bromide is a better leaving group.
No change in the rate of the reaction would be observed because it does not depend on the nature of the
halogen.
O The reaction would be faster because the C-Br bond is weaker than the C-CI bond.
O The reaction would be slower because the C-CI bond is weaker than the C-Br bond.
Transcribed Image Text:A student uses a-bromoacetic acid instead of a-chloroacetic acid for the reaction. Which statements below are correct? (Check all that apply) The reaction would be slower because bromide is a poorer leaving group. O The reaction would be faster because bromide is a better leaving group. No change in the rate of the reaction would be observed because it does not depend on the nature of the halogen. O The reaction would be faster because the C-Br bond is weaker than the C-CI bond. O The reaction would be slower because the C-CI bond is weaker than the C-Br bond.
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