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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
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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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: لحمد yasl R 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
Transcribed Image Text: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: لحمد yasl R 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
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