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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.

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.

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
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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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.
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
Step 1

Given that, a compound is

Chemistry homework question answer, step 1, image 1

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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