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.

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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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