H₂C CH3 CH3 CH Stereoisomers 1₂2 H₂ CH3 2,6-dimethyloct-2-ene CH3

Chemistry: Matter and Change
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Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
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Chapter21: Hydrocarbons
Section: Chapter Questions
Problem 94A
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    • 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
    • o illustrate the possible stereoisomers of the molecule.
H₂C
CH3
isomerism.
CH3
CH
Stereoisomers
H₂
H₂
C.
CH 3
C
CH3
Note
Check C6 again!
Write the calculation of the stereoisomers
2,6-dimethyloct-2-ene
Stereoisomerism: The structure does not have any chiral centers. So, they do not nave any
stereo isomers.
Geometrical isomerism: The structure cannot be distinguished with their geometrical
A compound can give stereo isomers if and only if it has at least one chiral carbon.
Your molecule also have a double bond which indicate that it can potentially have E-Z configuration.
If this do not apply, explain. (NOTE: E-Z configuration are not part of the stereoisomers)
Transcribed Image Text:H₂C CH3 isomerism. CH3 CH Stereoisomers H₂ H₂ C. CH 3 C CH3 Note Check C6 again! Write the calculation of the stereoisomers 2,6-dimethyloct-2-ene Stereoisomerism: The structure does not have any chiral centers. So, they do not nave any stereo isomers. Geometrical isomerism: The structure cannot be distinguished with their geometrical A compound can give stereo isomers if and only if it has at least one chiral carbon. Your molecule also have a double bond which indicate that it can potentially have E-Z configuration. If this do not apply, explain. (NOTE: E-Z configuration are not part of the stereoisomers)
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