Following statements
a) identify the most stable conformation for each of the compounds.
trans 1-isopropyl 3 methylcyclohexane b. cis-1-isopropyl-3-methylcyclohexane .
b) identify the number of steroisomers that 2.7-dimethylbicyclo [2.2.1] heptane has.
c) how would cis 3 methyl 1 cyclohexanol convert to cis 3-methyl-1-chlorocyclohexane?
d) in a chemical reaction of a chiral compound with a breakdown of the chiral carbon, what does configuration inversion mean?
e) order in an increasing manner according to the nucleophilic force of the halides in aqueous medium.
f) in the second chlorination (on c-2) of r 1 chloro 2 methylbutane what happens with the optical activity