• Part C The major product of the synthesis, 3-methoxyheptane, is produced by an SN2 mechanism. Complete the reaction mechanism below by adding curved arrows showing electron flow and the final product, including the correct stereochemistry, to demonstrate the formation of the major product (3-methoxyheptane). Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron-flow arrows should start on an atom or a bond and should end on an atom, bond, or location where a new bond should be created. » View Available Hint(s) D 2 C Q Q & H: gat 0 0 H Br

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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• Part C
The major product of the synthesis, 3-methoxyheptane, is produced by an SN2 mechanism. Complete the reaction mechanism below by adding curved arrows showing electron flow and the final product, including the correct stereochemistry, to demonstrate the formation of the
major product (3-methoxyheptane).
Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron-flow arrows should start on an atom or a bond and should end on an atom, bond, or location where a new bond
should be created.
, View Available Hint(s)
H
N
S
H;C
CH,
Br
ö-CH,
P
F
Transcribed Image Text:• Part C The major product of the synthesis, 3-methoxyheptane, is produced by an SN2 mechanism. Complete the reaction mechanism below by adding curved arrows showing electron flow and the final product, including the correct stereochemistry, to demonstrate the formation of the major product (3-methoxyheptane). Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron-flow arrows should start on an atom or a bond and should end on an atom, bond, or location where a new bond should be created. , View Available Hint(s) H N S H;C CH, Br ö-CH, P F
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