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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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?
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