2) ) Draw a perspective diagram (dashwedge) of (S)-1-bromo-1-fuoroethane Only use dashwedge for the chirality center, and show your CIP. priorities to prove the (S)- designation ) Draw a detailed mechanism showing the formation of the major productis) of the reaction betwoen (S)-1-bromo-1-fuoroethane and sodium methoxide (NaOCH, the Na" is a spectator) Please be sure to include all structures (use perspective diagrams as appropriate to illustrate the storeochemistry of the process), resonance forms, intermediates, transition states, curved arrows, formal charges, or lone pairs as necessary. iI) Please redraw your product(s) below and assign (R/S) to the chirality center(s) therein (please show your CIP priorities). Is the mechanism Sy1 or S2, and what is the overall stereochemistry associated with the process? Why is this an interesting case?

Chemistry
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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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2) ) Draw a perspective diagram (deshwedge) of (S)-1-bromo-1-fuoroethane
Orly use dash'wedge for the chirality center, and show your CIP. priorities to
prove the (S)-designation.
I) Draw a detailed mechanism showing the formation of the major product(s) of the reaction
between (S)-1-bromo-1-fluoroethane and sodium methoxide (NaOCH, the Na" is a spectator)
Please be sure to include all structures (use perspective diagrams as appropriate to illustrate the
stereochemistry of the process), resonance forms, intermediates, transition states, curved arrows,
formal charges, or lone pairs as necessary.
i) Please redraw your product(s) below and assign (R/S) to the chirality center(s) therein.
(please show your C.IP priorities). Is the mechanism Sy1 or Sy2, and what is the overall
stereochemistry associated with the process? Why is this an interesting case?
Periodic Table t
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Transcribed Image Text:2) ) Draw a perspective diagram (deshwedge) of (S)-1-bromo-1-fuoroethane Orly use dash'wedge for the chirality center, and show your CIP. priorities to prove the (S)-designation. I) Draw a detailed mechanism showing the formation of the major product(s) of the reaction between (S)-1-bromo-1-fluoroethane and sodium methoxide (NaOCH, the Na" is a spectator) Please be sure to include all structures (use perspective diagrams as appropriate to illustrate the stereochemistry of the process), resonance forms, intermediates, transition states, curved arrows, formal charges, or lone pairs as necessary. i) Please redraw your product(s) below and assign (R/S) to the chirality center(s) therein. (please show your C.IP priorities). Is the mechanism Sy1 or Sy2, and what is the overall stereochemistry associated with the process? Why is this an interesting case? Periodic Table t Upload Choose a File MacBook Pro esc $4 % & 3 5 Q W E R T Y tab A F G H caps lock C V ift control option command く0 の
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