1. Occasionally, a crossed Cannizzaro reaction is carried out to reduce benzaldehyde derivatives to the corresponding benzyl alcohol, utilizing formaldehyde as the reducing agent. i) Please show the mechanism by which this occurs. ii) Why is this method'effecti ve? That is, why are the principal products benzyl alcohol and formic acid and not benzoic acid and methanol?
1. Occasionally, a crossed Cannizzaro reaction is carried out to reduce benzaldehyde derivatives to the corresponding benzyl alcohol, utilizing formaldehyde as the reducing agent. i) Please show the mechanism by which this occurs. ii) Why is this method'effecti ve? That is, why are the principal products benzyl alcohol and formic acid and not benzoic acid and methanol?
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:1. Occasionally, a crossed Cannizzaro reaction is carried out to reduce benzaldehyde
derivatives to the corresponding benzyl alcohol, utilizing formaldehyde as the
reducing agent.
i) Please show the mechanism by which this occurs.
ii) Why is this method'effective? That is, why are the principal products benzyl alcohol
acid and not benzoic acid and methanol?
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