Once you have completed this question please show your work to the camera and then immediately submit a PDF of your answer to 'Exam 2 Free RSubmission' in the Exam 2 module. The time stamps for the end of your lockdown session and PDF submission cannot be more than 5 minutes aparDQuestion 112 p2) i) Draw a perspective diagram (dash/wedge) of (S)-1-bromo-1-fluoroethane.Only use dash/wedge for the chirality center, and show your C.I.P. priorities toprove the (S)- designation.ii) Draw a detailed mechanism showing the formation of the major product(s) of the reactionbetween (S)-1-bromo-1-fluoroethane and sodium methoxide (NaOCH3; the Na* is a spectator).Please be sure to include all structures (use perspective diagrams as appropriate to illustrate thestereochemistry of the process), resonance forms, intermediates, transition states, curved arrows,formal charges, or lone pairs as necessary.iii) Please redraw your product(s) below and assign (R/S) to the chirality center(s) therein.(please show your C.I.P priorities). Is the mechanism Sy1 or Sy2, and what is the overallstereochemistry associated with the process? Why is this an interesting case?Periodic TableUploadChoose a FileMacBook Pro56WeERtabFGCADS lookCaption

R/S nomenclature is based on CIP rule which states that higher is the atomic number of directly…

2) i) Draw a perspective diagram (dash/wedge) of (S)-1-bromo-1-fluoroethane. Only use dash/wedge for the chirality center, and show your C.I.P. 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. iii) Please redraw your product(s) below and assign (R/S) to the chirality center(s) therein. (please show your C.I.P priorities). Is the mechanism SN1 or SN2, and what is the overall stereochemistry associated with the process? Why is this an interesting case?

2) i) Draw a perspective diagram (dash/wedge) of (S)-1-bromo-1-fluoroethane. Only use dash/wedge for the chirality center, and show your C.I.P. 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. iii) Please redraw your product(s) below and assign (R/S) to the chirality center(s) therein. (please show your C.I.P priorities). Is the mechanism SN1 or SN2, and what is the overall stereochemistry associated with the process? Why is this an interesting case?

Principles of Instrumental Analysis

7th Edition

ISBN:9781305577213

Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch

Publisher:Douglas A. Skoog, F. James Holler, Stanley R. Crouch

Chapter1: Introduction

Section: Chapter Questions

Problem 1.12QAP

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