When reducing this compound with NaBH4 might reduce either the aldehyde or ketone. H Draw the final products. Identify and describe one unambiguous and unique peak (THAT IS NOT AN OH) in each potential product. H NMR spectrum that would tell you which carbonyl group had been reduced.
When reducing this compound with NaBH4 might reduce either the aldehyde or ketone. H Draw the final products. Identify and describe one unambiguous and unique peak (THAT IS NOT AN OH) in each potential product. H NMR spectrum that would tell you which carbonyl group had been reduced.
Chapter31: An Oxidation–reduction Scheme: Borneol, Camphor, Isoborneol
Section: Chapter Questions
Problem 5Q
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![When reducing this compound with NaBH4 might reduce either the aldehyde or ketone.
H
Draw the final products.
Identify and describe one unambiguous and unique peak (THAT IS NOT AN OH) in each
potential product. H NMR spectrum that would tell you which carbonyl group had been reduced.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fbe5686f9-a7ee-435c-bafc-4f010a404b82%2F24df9f41-c5f3-422c-af49-be7f69a4b084%2Fu3xx8tm_processed.png&w=3840&q=75)
Transcribed Image Text:When reducing this compound with NaBH4 might reduce either the aldehyde or ketone.
H
Draw the final products.
Identify and describe one unambiguous and unique peak (THAT IS NOT AN OH) in each
potential product. H NMR spectrum that would tell you which carbonyl group had been reduced.
Expert Solution
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Step 1
Given that, a compound is
We have to tell which carbonyl group either aldehyde or ketone will reduced by the NaBH4.
Introduction: Selective reduction of carbonyl compound.
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