Organic Chemistry HW: CANNOT BE HAND DRAWN 2,6-dimethyloct-2-ene Provide a detailed typed explanation of Stereoisomers show the expanded structure of your molecule. Calculate the maximum number of possible stereoisomers of your molecule using the following formula: Maximum number of possible stereoisomers = 2n (where n= the number of chiral carbons in your molecule). This calculation does not include E- or Z- isomers for any compounds containing double bonds Type or using a computer program "draw" the possible stereoisomers of the molecule. Note that E-, Z- isomers of each stereoisomer are also possible and would not be accounted for by the formula above; draw any E- or Z- isomers.

What is the mathematical relationship between the number of chiral carbons and the number of optical isomers (stereoisomers) in a molecule?

Draw the structure for 2-bromo-2-chloro-3,4-dimethylhexane and state which if any carbons are chiral using the carbon number. Example: C1.

2-brokopentane is an optically active compound, draw the two possible structure of optical isomer and label the chiral center with an asterisk(*) in each of the optical isomer structure

Examine the structure of PGF2a. Identify all chiral centers and all double bonds about which cis,trans isomerism is possible and state the number of stereoisomers possible for a molecule of this structure.

Name the family to which each organic compound belongs.

What is the structure of SeF5NF2?

What is isomer? Name by typing the isomers of the compound whose closed formula is C4H9Cl. Which of these isomers can have chiral structure. Examine it from a stereochemical point of view.

If a research paper appeared reporting the structure of a new molecule with formula C2H8 , most chemists would be highly skeptical. Why?