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Organic Chemistry: A Guided Inquiry

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter10: Oxidation And Reduction

Section: Chapter Questions

Problem 13E

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Question

3. In the box provided, draw the lowest energy Newman projection (looking down the bond
indicated) that corresponds to the compound drawn. (4 points total, 2 points per box)
a)
b)

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4) Draw the most stable and least stable Newman projections of the following compound viewed along the indicated bond. Br H
Observe the Newman projection of the next molecule along the bond shown in red with the front carbon the one bonded to "Cl". a) Draw one of the Newman projections of the molecule with a staggered conformation. b) Draw one of the Newman projections of the molecule with an eclipsed conformation.
What is the resonanace for each molecule in second picture.
C Draw the most stable Newman projection for each of the labeled C-C bonds: ...... A A .D D B
Draw an arrow on the carbocation in the box on the left to show how it rearranges to the carbocation in the box on the right.
Draw the lowest energy Newman projection of the molecule on the left looking down the bond indicated for molecule A. For molecules B and C, draw the lowest energy chair conformations.
4. Draw a Newman projection of the following compound that centers along the marked bond. This one! CH3 CH3 + + H
draw newman projection for the indicated bond. put largest groups anti to each other.
A) Which one is more stable? B) Which one is more stable?
answer c and d please
a) Draw a Newmann Projection of the following compound looking down the indicated bond (Ph represents a benzene ring). Br b) Using a Newmann Projection draw a conformation of this molecule where the bromine and hydrogen are in an anti-conformation
a. Draw the Newman projection for each molecule shown here, looking down the c-c bond indicated by the arrow. b. Which configuration do you think is more stable? Explain.

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