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 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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