(a)
Interpretation:
The presence of asymmetric centers in the given compounds has to be checked.
Concept introduction:
Stereoisomers are isomers which have different spatial arrangement in spite of same bond connectivity. Stereoisomers are due to the presence of stereo center.
Asymmetric center is a stereo center which arises to hydrocarbons if the carbon is bonded to four different groups.
(b)
Interpretation:
The chirality of the given compounds has to be checked.
Concept introduction:
Optical activity (chirality) of a molecule is the interaction between molecule and plane-polarized light.
Molecule having asymmetric center shows optical activity except mesocompounds.
If a compound having non-superimposable mirror image, then the compound is chiral.
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Chapter 4 Solutions
Organic Chemistry
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- Under what conditions is a carbon atom a chiral center? A. if it has no stereoisomers B. if the molecule that it belongs to can be superimposed on its mirror image after rotation C. if it is symmetric D. if it has four different substituent groupsarrow_forwardConsider molecules with more than one chiral center. Consider 2,3-dyhdroxybutanoic acid. a. How many chiral centers does it have? b. Which ones? c. Reproduce the structure and encircle the four groups, which are linked to each chiral carbon.arrow_forwardIdentify which of the compound is chiral.a. T-butyl alcoholb. 2,2-dimethylpropanec. 1,2,4,5-tetramethylcyclohexaned. 2-hydroxypropanoic acidarrow_forward
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