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
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Question 2 please

Transcribed Image Text:Draw the Newman Projections with the highest and lowest energy
for the molewkes
below. Sight along the bond
of the
a) Cl - CH₂ - CH₂ - Bv
C) In the molewles above, explain why
the
highest energy.
Do
b)
a
1b.
CHÍCH - CHÍ CH
F
full conformational analysis
the
conformers
highlighted Carbons.
for the
conformer you drew is
molewle drawn
Expert Solution

Step 1: Introduction
To understand and visualize easily the conformations of the compound we will represent each conformation in Newman representation.
Eclipse structures in Newman representation are higher than the staggered structures.
A total six conformations are possible for any bond between two sp3 hybridized atoms. Keeping one carbon centre and by rotating 60o another centre each time we will get one new conformation, until the starting structure is reached.
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Solved in 3 steps with 3 images
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