Newman projections viewed through the C3-C4 bond (C3 in the front, C4 in the back). Write the relevant conformations in 60° increments, indicate whether they are eclipsed or staggered, gauche, anti, or syn, and plot their Br ative potential energy. As you plot their relative potential energy, consider the propyl group on carbon 3 to be bulkier than the bromo group on carbon 3.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter6: Alkanes & Alkenes
Section: Chapter Questions
Problem 4E: Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This...
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Perform a conformational analysis of 3-bromo-2-methylpentane using
Newman projections viewed through the C3-C4 bond (C3 in the front, C4 in
the back). Write the relevant conformations in 60° increments, indicate
whether they are eclipsed or staggered, gauche, anti, or syn, and plot their
Br
relative potential energy. As you plot their relative potential energy, consider the
isopropyl group on carbon 3 to be bulkier than the bromo group on carbon 3.
5.
Transcribed Image Text:Perform a conformational analysis of 3-bromo-2-methylpentane using Newman projections viewed through the C3-C4 bond (C3 in the front, C4 in the back). Write the relevant conformations in 60° increments, indicate whether they are eclipsed or staggered, gauche, anti, or syn, and plot their Br relative potential energy. As you plot their relative potential energy, consider the isopropyl group on carbon 3 to be bulkier than the bromo group on carbon 3. 5.
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