5. Provide major substitution product and the reaction mechanism for its formation.
6. Draw the structural representation for the most stable Newman Projection for 5-chloro-4, 6-diethyl-2,3-dimethyloctane from rotation about C(4) –C(5) bond.
7. Arrange the following carbocations in order of their decreasing stability.
8. Provide the stereochemistry of the following compounds.
9. What is a meso compound?
Draw a Fischer Projection of a meso compound of your choice.
10. Provide the IUPAC names of the following compound.
11. Draw the structure of the compound,
(2Z, 4E) -6-bromo-2-chloro-5-ethyl-4-methyl-2,4-heptadien-3-ol