Concept explainers
(a)
Interpretation:
The enantiomers of the given compounds using perspective formula has to be drawn.
Concept introduction:
Enantiomers are stereoisomers of compounds having one asymmetric center, in which these isomers are non-superimposable mirror images of each other.
Enantiomers can be drawn using perceptive formals or Fischer projections.
Perceptive formula: draw two bonds of asymmetric carbon is in plane, one bond as a solid wedge that coming out of plane and the fourth bond as hatched wedge that pointing away from the plane. T he solid wedge is always below to the hatched wedge.
Fischer projections: the asymmetric center (carbon) represents as the point of intersection of two perpendicular lines, in which the horizontal lines represent the bonds that project out of the plane of the paper and the vertical lines represent the bonds that away from the plane of the paper.
(b)
Interpretation:
The enantiomers of the given compounds using fisher projection has to be drawn.
Concept introduction:
Enantiomers are stereoisomers of compounds having one asymmetric center, in which these isomers are non-superimposable mirror images of each other.
Enantiomers can be drawn using perceptive formals or Fischer projections.
Perceptive formula: draw two bonds of asymmetric carbon is in plane, one bond as a solid wedge that coming out of plane and the fourth bond as hatched wedge that pointing away from the plane. The solid wedge is always below to the hatched wedge.
Fischer projections: the asymmetric center (carbon) represents as the point of intersection of two perpendicular lines, in which the horizontal lines represent the bonds that project out of the plane of the paper and the vertical lines represent the bonds that away from the plane of the paper.
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Chapter 4 Solutions
Organic Chemistry, Books a la Carte Edition (8th Edition)
- For the following Fischer projection answer the following: a. How many stereo isomers are possible? b. Assign each chiral center R or S. c. Name the compound including the absolute configuration, R or S. d. Draw and name the stereo isomers (enantiomers, diastereomers, and meso it present). INO2 CI INO2arrow_forwardShow two different rearrangement products for the carbocation shown below. Circle the rearrangement product that is preferred (more likely to form). 04 Attach File Browse Local Filesarrow_forward2. What is the relationship between these two molecules? o a. Identical b. Constitutional isomers c. Enantiomers d. Diastereomersarrow_forward
- Draw the structure for a compound with molecular formula C2H2I2F2 a. that is optically inactive because it does not have an asymmetric center. b. that is optically inactive because it is a meso compound. c. that is optically active.arrow_forward1. An object is chiral if it A. is superimposable on its mirror image B. is not superimposable on its mirror image C. has no mirror image D. is identical to each mirror image of itselfarrow_forward2. Draw enantiomers for each of the following using. a. perspective formulas. b. Fischer projections. Br CH3 CH3CHCH₂OH CH3CHCHCH3 OHarrow_forward
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- What are I and II? A.) Identical B.) Diastereomers C.) Constitutional isomers D.) Enantiomersarrow_forwardDetermine the relationship between the two drawings: A. Enantiomers B. Same compound C. Constitutional isomers D. Diastereomersarrow_forwardThese two products are a. diastereomers b. constitutional isomers c. identicalarrow_forward
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