1. Make a model of each compound, draw it in its most symmetric conformation, anddetermine whether it is capable of showing optical activity.
(a) 1-bromo-1-chloroethane (b) 1-bromo-2-chloroethane
(c) 1,2-dichloropropane (d) cis-1,3-dibromocyclohexane
(e) trans-1,3-dibromocyclohexane (f) trans-1,4-dibromocyclohexane
2. Star (*) each asymmetric carbon atom, label each as (R) or (S), and compare your resultfrom part (1) with the prediction you would make based on the asymmetric carbons.
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