Solve all parts completely otherwise I will downvote. 1. Observe the Lewis structure of the nitro-group compared to the ketone (carbonyl). Why do youthink the reductions had different outcomes? Is there any clear difference in reactivity betweenthe two functional groups? If one functional group is clearly more reactive, why did the strongerreduction reaction still not react the other functional group?2. Based on your results, what would the outcome of each of the following reactions be?SnHCl aq.NO2NABH,ethanolNO2SnHCl aq.

The functional group interconversion is a key reaction utilized in synthetic organic chemistry in…

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Solve all parts completely otherwise I will downvote.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter10: Alcohols

Section: Chapter Questions

Problem 10.50P

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Question

Solve all parts completely otherwise I will downvote.

1. Observe the Lewis structure of the nitro-group compared to the ketone (carbonyl). Why do you
think the reductions had different outcomes? Is there any clear difference in reactivity between
the two functional groups? If one functional group is clearly more reactive, why did the stronger
reduction reaction still not react the other functional group?
2. Based on your results, what would the outcome of each of the following reactions be?
Sn
HCl aq.
NO2
NABH,
ethanol
NO2
Sn
HCl aq.

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