Chapter 4: Q78P (page 143)
Using skeletal structures, draw the stereoisomers of
a. 2,4-dichloroheptane. b. 2,4-dichloropentane.
Short Answer
We have to draw the structures of stereoisomers of following compounds:
a)
b)
Chapter 4: Q78P (page 143)
Using skeletal structures, draw the stereoisomers of
a. 2,4-dichloroheptane. b. 2,4-dichloropentane.
We have to draw the structures of stereoisomers of following compounds:
a)
b)
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Get started for freeWhich of the following has an achiral stereoisomer?
A 2,3-dichlorobutane
B 2,3-dichloropentane
C 2,3-dichloro-2,3-dimethylbutane
D 1,3-dichlorocyclopentane
E 1,3-dibromocyclobutane
F 2,4-dibromopentane
G 2,3-dibromopentane
H 1,4-dimethylcyclohexane
I 1,2-dimethylcyclopentane
J 1,2-dimethylcyclobutane
Identify whether each of the structure in the second row is an enantiomer of, is a diastereomer of, or is identical to the structure in the top row.
Question:
a. Draw all possible stereoisomers of the following compound:
b. Which stereoisomers are optically inactive?
The reaction of (R)-1-iodo-2-methylbutane with hydroxide ion forms an alcohol without breaking any bonds to the asymmetric centre. The alcohol rotates the plane of polarization of plane-polarized light counter clockwise. What is the configuration of (+)-2-methyl-1-butanol?
Question:
a. Draw all the isomers with molecular formula C6H12 that contain a cyclobutane ring. (Hint: There are seven.)
b. Name the compounds without specifying the configuration of any asymmetric centers.
c. Identify
1. constitutional isomers 2. Stereoisomers 3. cis–trans isomers 4. chiral compounds
5. achiral compounds 6. Meso compounds 7. Enantiomers 8. diastereomers
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