Convert the chair isomer into a flat cyclohexane representation (being sure to preserve the stereochemical information). 

b) draw the mechanism for deprotonating the acidic functional group found in your molecule and the final product. (give me an explanation too please)

c) Show the acid/base mechanism for the deprotonation of your acid functional group 

D) state what the pKa of the functional group you are deprotonating explain what the arrows were showing using appropriate terminology.

 

CI- OH