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?

1. reactive feature, determine what it needs, show the reaction, and continue the process until you find the major stable product(s) of the reaction. As applicable, also state the stereochemistry of any chirality center created by the reaction and use either Fisher projection or perspective formula representations to draw the product showing the correct representation for the stereochemistry. Label the reactive features of the following set of reactants, select the most 1,2-dimethylcyclohexene + BH; followed by H;O2, "OH, and H;O

Please don't provide handwriting solution

This question is from a study guide for o-chem.  If you can please help me understand the steps of the reaction and help me break it down a bit i would really appreciate it.