in a reaction where trans-stilbene reacts with a molecule of bromine while using ethanol as a solvent, what would happen if the ethanol was a more reactive nucleophile than the bromide ion(s)? what would the product look like?

in a reaction where trans-stilbene reacts with a molecule of bromine while using ethanol as a solvent, what would happen if the ethanol was a more reactive nucleophile than the bromide ion(s)? what would the product look like?

Chemistry for Today: General, Organic, and Biochemistry

9th Edition

ISBN:9781305960060

Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Chapter14: Aldehydes And Ketones

Section: Chapter Questions

Problem 14.55E: The addition of water to aldehydes and ketones occurs rapidly, although it is not thermodynamically...

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