a.
Interpretation:
For the clopidogrel compound the chirality centers has to be labeled and number of chiral centers should be determined
Concept introduction:
Chirality center:
When a carbon atom is bonded to four different groups, then that carbon is named as chiral carbon and it is called as chirality center. Generally, the carbon atom contains tetrahedral valency, therefore it bonded to four atoms or molecules. The chiral center is bonded with four different elements or groups. If the single carbon atom is bonded to two or more identical group or atom, then it is also not considered as chiral carbon. In addition to this, if the carbon atom contains multiple bond then it does not able to bond with four different groups then it is not considered to be as a chirality center.
b.
Interpretation:
For the clopidogrel compound, Fischer projection formula has to be drawn.
Concept introduction:
Fischer projections:
In Fischer projection, the chirality center of the organic compounds are drawn using the following convention. First, the carbon atom is placed at the meeting point of the two lines of the cross. In a tetrahedron structure, the horizontal bonds indicate forward and denoted by wedges. The vertical bonds indicate backward and denoted by dashed lines. Finally, Fischer projection structure is abbreviated by cross formula.
Enantiomers:
Enantiomers are mirror image of one another and these are chiral molecules, but that are non superimposable on one another.
Want to see the full answer?
Check out a sample textbook solutionChapter 12 Solutions
Connect 1-Semester Online Access for Principles of General, Organic & Biochemistry
- Trabectedin, shown in a ball-and-stick model on the cover of this text, is an anticancer drug sold under the trade name Yondelis. a. Locate the stereogenic centers in trabectedin. b.What is the maximum number of stereoisomers possible for trabectedin? c.Draw the enantiomer. d.Draw a diastereomer. e.If the specific rotation of trabectedin is +41.5, what is the [α] of a solution that contains 75% trabectedin and 25% of its enantiomer?f . What is the ee of a solution with [α] = +10.5?arrow_forwardRe-draw each Fischer projection formula using wedges and dashed wedgesfor the stereogenic center, and label the center as R or S.arrow_forwardDraw both enantiomers of clopidogrel (trade name Plavix), a drug given to prevent the formation of blood clots in persons who have a history of stroke or coronary artery disease. Plavix is sold as a single enantiomer with the S configuration. Which enantiomer is Plavix?arrow_forward
- Draw each stereogenic center using a Fischer projection formula.arrow_forwardLocate the stereogenic centers in each drug. Albuterol is a bronchodilator—that is, it widens airways—so it is used to treat asthma. Chloramphenicol isan antibiotic used extensively in developing countries because of its lowcost.arrow_forwardC. Smelling Chirality. Carvone Olfactory receptors in our noses, used for the detection of odors, are chiral. Therefore, in some cases, we can tell the difference between enantiomers by their odor. Carvone is one such compound that we can distinguish between the R and S enantiomer by their odor. 1. Identify the chiral center in carvone and draw the R and S enantiomers in the indicated boxes. 2. Smell both of the enantiomers of carvone and provide a brief description of their odors in the same boxes. Carvone is perfectly safe to smell as both enantiomers are found in various foods. R-carvone S-carvonearrow_forward
- Consider the following molecules (a-h) and answer the questions below:i. How many chiral carbon does it contains?ii. Does the molecule have any internal plane of symmetry?iii. Identify the molecule whether it is chiral of achiral?iv. Does it rotate the plane of polarized light?v. Is the molecule optically active?vi. Is meso compound present?vii. Draw all possible stereoisomers for the molecule in Fischer projection and label the relationship between each of the isomer.arrow_forwardCaptopril is a drug used to treat high blood pressure and congestiveheart failure.Designate each stereogenic center as R or S.arrow_forwardAlthough fresh human sweat has no odor, enzymes in skin bacteria form a variety of compounds with distinctive, pungent odors. The two enantiomers of 3-methyl-3-sulfanyl-1-hexanol (A), which smell somewhat differently, contribute to the characteristic foul odor of sweat. Locate the chirality center in A and draw both enantiomersarrow_forward
- Help with orgo questionarrow_forwardDraw both enantiomers of clopidogrel (trade name Plavix), a drug given to prevent the formation of blood clots in persons who have a history of stroke or coronary artery disease. Plavix is sold as a single enantiomer with the S configuration. Which enantiomer is Plavix?arrow_forwardTrabectedin, shown in a ball-and-stick model on the cover of this text, isan anticancer drug sold under the trade name Yondelis. Question: a.) Draw the enantiomer. b.) Draw a diastereomer.arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY