could a primary alcohol be oxidized to a ketone using the same oxidation of isoborneol using bleach and acetic acid? the mechanism is below for reference: yeat. H₂O •H₂o* cr no because it would form an unstabilized carbocation yes because primary alcohols are less acidic yes because there is still a hydrogen available to be deprotonated on the same carbon as the alcohol no because of the extra hydrogen attached to the same carbon as the alcohol

could a primary alcohol be oxidized to a ketone using the same oxidation of isoborneol using bleach and acetic acid? the mechanism is below for reference: yeat. H₂O •H₂o* cr no because it would form an unstabilized carbocation yes because primary alcohols are less acidic yes because there is still a hydrogen available to be deprotonated on the same carbon as the alcohol no because of the extra hydrogen attached to the same carbon as the alcohol

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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