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.
Trending nowThis is a popular solution!
Chapter 4 Solutions
Organic Chemistry (8th Edition)
- Instructions: Label each pair of stereoisomers as:a. enantiomersb. diastereomersc. identicalarrow_forward2. What is the relationship between these two molecules? o a. Identical b. Constitutional isomers c. Enantiomers d. Diastereomersarrow_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_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_forward2. Draw enantiomers for each of the following using. a. perspective formulas. b. Fischer projections. Br CH3 CH3CHCH₂OH CH3CHCHCH3 OHarrow_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_forward
- Classify each compound as IDENTICAL to A or an ENANTIOMER to A.arrow_forwarda. Which of these two can exist as a pair of enantiomers?b. Draw the pair of enantiomers using three-dimensional representation.arrow_forward4.) Label each pair of compounds with the best choice from below: A. Enantiomers A.) a Bile=20 B.) B. Diastereomers C.) B C. Constitutional Isomers 8 11*** D.) d E.) e D. Identical Compounds Br. F) Bl me E. None *****arrow_forward
- Determine 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_forward4. Draw enantiomers for each of the following compounds using Fischer projections and skeletal structures with dash-wedge notation. bavogmos simsa A. B. C. CH3 FO Br F OH CH3 .0arrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning