5:42 PM Sat Jun 29 kennesaw.view.usg.edu Task 2: Molecular Modeling of 2-chlorobutane Assemble the model of 2-chlorobutane. Manipulate and visualize the model according to the instructions provided in each problem. CI 4 3 2-chlorobutane Problem 2(A): Build a model of 2-chlorobutane. Identify the asymmetric center (also known as “chiral” center or "chirality” center) and orient the model so that the “H” on the asymmetric center points away from you. Now, place the model of 2-chlorobutane on the bench in front of you and imagine a mirror standing next to it. Construct a model of its mirror image. Complete the line and wedge templates provided on the next page by supplying the missing substituents. asymmteric center ...H Hi Problem 2(B): Assign R/S configuration to the asymmetric center in the representations you have drawn above. Show how you identify the order of priority various substituents. Priority 1: Priority 2: Priority 3: Priority 4: Problem 2(C): Without breaking any bonds, rotate the models to investigate if 2-chlorobutane and its mirror image model are superimposable on each other. Are the two models superimposable? Circle the words that correctly describe the relationship between (R)-2-chlorobutane and (S)-2-chlorobutane? Constitutional isomers Stereoisomers Enantiomers Diastereomers 33%

Human Anatomy & Physiology (11th Edition)
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Author:Elaine N. Marieb, Katja N. Hoehn
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Chapter1: The Human Body: An Orientation
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5:42 PM Sat Jun 29
kennesaw.view.usg.edu
Task 2: Molecular Modeling of 2-chlorobutane
Assemble the model of 2-chlorobutane. Manipulate and visualize the model according to the instructions provided in
each problem.
CI
4
3
2-chlorobutane
Problem 2(A): Build a model of 2-chlorobutane. Identify the asymmetric center (also known as “chiral” center or
"chirality” center) and orient the model so that the “H” on the asymmetric center points away from you. Now, place
the model of 2-chlorobutane on the bench in front of you and imagine a mirror standing next to it. Construct a model
of its mirror image. Complete the line and wedge templates provided on the next page by supplying the missing
substituents.
asymmteric center
...H
Hi
Problem 2(B): Assign R/S configuration to the asymmetric center in the representations you have drawn above. Show
how you identify the order of priority various substituents.
Priority 1:
Priority 2:
Priority 3:
Priority 4:
Problem 2(C): Without breaking any bonds, rotate the models to investigate if 2-chlorobutane and its mirror image
model are superimposable on each other.
Are the two models superimposable?
Circle the words that correctly describe the relationship between (R)-2-chlorobutane and (S)-2-chlorobutane?
Constitutional isomers
Stereoisomers
Enantiomers
Diastereomers
33%
Transcribed Image Text:5:42 PM Sat Jun 29 kennesaw.view.usg.edu Task 2: Molecular Modeling of 2-chlorobutane Assemble the model of 2-chlorobutane. Manipulate and visualize the model according to the instructions provided in each problem. CI 4 3 2-chlorobutane Problem 2(A): Build a model of 2-chlorobutane. Identify the asymmetric center (also known as “chiral” center or "chirality” center) and orient the model so that the “H” on the asymmetric center points away from you. Now, place the model of 2-chlorobutane on the bench in front of you and imagine a mirror standing next to it. Construct a model of its mirror image. Complete the line and wedge templates provided on the next page by supplying the missing substituents. asymmteric center ...H Hi Problem 2(B): Assign R/S configuration to the asymmetric center in the representations you have drawn above. Show how you identify the order of priority various substituents. Priority 1: Priority 2: Priority 3: Priority 4: Problem 2(C): Without breaking any bonds, rotate the models to investigate if 2-chlorobutane and its mirror image model are superimposable on each other. Are the two models superimposable? Circle the words that correctly describe the relationship between (R)-2-chlorobutane and (S)-2-chlorobutane? Constitutional isomers Stereoisomers Enantiomers Diastereomers 33%
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