OH H 4. Pseudoephedrine (Sudafed, PSE) is a sympathomimetic drug of the phenethylamine and amphetamine chemical classes. It may be used as a nasal/sinus decongestant, as a stimulant, or as a wakefulness-promoting agent in higher doses. Given the structure of PSE (right): a. Draw a Newman projection that results from viewing down C1-C2, as indicated by the arrow. (6) b. Draw the highest energy Newman projection and comment on what makes this conformation thermodynamically unstable relative to other conformations. (5) Consult the lowest energy conformation about the C1-C2 bond axis to postulate a key IMF that helps to stabilize the lowest energy conformation. Indicate this IMF on your Newman projection in part (a). (5) c.

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...
icon
Related questions
Question

A1

OH H
4. Pseudoephedrine (Sudafed, PSE) is a sympathomimetic drug of
the phenethylamine and amphetamine chemical classes. It may
be used as a nasal/sinus decongestant, as a stimulant, or as
a wakefulness-promoting agent in higher doses. Given the
structure of PSE (right):
a. Draw a Newman projection that results from viewing down
C1-C2, as indicated by the arrow. (6)
b.
c.
Draw the highest energy Newman projection and comment on what makes this
conformation thermodynamically unstable relative to other conformations. (5)
Consult the lowest energy conformation about the C1-C2 bond axis to postulate a
key IMF that helps to stabilize the lowest energy conformation. Indicate this IMF on
your Newman projection in part (a). (5)
Transcribed Image Text:OH H 4. Pseudoephedrine (Sudafed, PSE) is a sympathomimetic drug of the phenethylamine and amphetamine chemical classes. It may be used as a nasal/sinus decongestant, as a stimulant, or as a wakefulness-promoting agent in higher doses. Given the structure of PSE (right): a. Draw a Newman projection that results from viewing down C1-C2, as indicated by the arrow. (6) b. c. Draw the highest energy Newman projection and comment on what makes this conformation thermodynamically unstable relative to other conformations. (5) Consult the lowest energy conformation about the C1-C2 bond axis to postulate a key IMF that helps to stabilize the lowest energy conformation. Indicate this IMF on your Newman projection in part (a). (5)
Expert Solution
steps

Step by step

Solved in 3 steps with 2 images

Blurred answer
Knowledge Booster
Representations of Organic Compounds
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY