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 beloware 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 thehalogen.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.

Given:The Williamson ether synthesis is used to prepare ethers.

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.

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.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter8: Addition Via Carbocation

Section: Chapter Questions

Problem 4E: Draw the complete mechanism of each pair of reactants including any favorable rearrangements and all...

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