1) Construct a model of the cyclic alkane: cyclopentane (C5H₁0). Because the five carbon atoms are locked in a ring, rotation about the single bonds is restricted; the plane of the ring is a fixed geometry within the molecule. Toggle between full Lewis structures and skeletal structures by clicking the C-H tool. Model 1: Use the solid wedge tool to attach a methyl group to each of two different carbon atoms in the cyclopentane. Note the five carbons of the ring are in the plane of the paper, and the solid wedge indicates both methyls project forward, in front of the plane of the paper. Model 2: Use the solid wedge tool to attach first methyl group to one of two different carbon atoms in the cyclopentane, and use the dashed wedge tool to attach the second. Note the solid wedge indicates that one methyl projects forward, in front of the plane of the paper. The dashed wedge indicates the other methyl extends back, behind the plane of the paper. Click the broom to tidy up the structures; convert each to a three-dimensional ball-and-stick model by clicking the 2D to 3D tool. Take a screen prints of your MolView structures, showing both the Lewis structure and 3D model. 2) Draw a condensed structure for each of the two models that you build. That is, draw a five-membered ring to represent the cyclopentane, and use CH3- groups to represent the two methyl substituents. Make certain that your structures clearly illustrate the arrangement of the methyl substituents with

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
icon
Related questions
Question
Draw two more molecules that are structural isomers of one another, as well as structural isomers of the cis/trans pair
above. Then write the IUPAC name for each structure.
Model 3 (structural isomer)
IUPAC Name:
IUPAC Name:
Model 4 (structural isomer)
Transcribed Image Text:Draw two more molecules that are structural isomers of one another, as well as structural isomers of the cis/trans pair above. Then write the IUPAC name for each structure. Model 3 (structural isomer) IUPAC Name: IUPAC Name: Model 4 (structural isomer)
B. Cycloalkanes
1) Construct a model of the cyclic alkane: cyclopentane (C5H₁0). Because the five carbon atoms are locked in a ring,
rotation about the single bonds is restricted; the plane of the ring a fixed geometry within the molecule. Toggle between
full Lewis structures and skeletal structures by clicking the C-H tool.
Model 1: Use the solid wedge tool to attach a methyl group to each of two different carbon atoms in the cyclopentane.
Note the five carbons of the ring are in the plane of the paper, and the solid wedge indicates both methyls project forward,
in front of the plane of the paper.
Model 2: Use the solid wedge tool to attach first methyl group to one of two different carbon atoms in the cyclopentane,
and use the dashed wedge tool to attach the second. Note the solid wedge indicates that one methyl projects forward, in
front of the plane of the paper. The dashed wedge indicates the other methyl extends back, behind the plane of the paper.
Click the broom to tidy up the structures; convert each to a three-dimensional ball-and-stick model by clicking the 2D to 3D
tool. Take a screen prints of your MolView structures, showing both the Lewis structure and 3D model.
2) Draw a condensed structure for each of the two models that you build. That is, draw a five-membered
ring to represent the cyclopentane, and use CH3- groups to represent the two methyl substituents.
Make certain that your structures clearly illustrate the arrangement of the methyl substituents with
respect to the fixed geometry of the cyclopentane ring.
Write the IUPAC name for each structure, keeping in mind that the name should specifically describe not
only the number of each type of atom and how they are connected, but also the arrangement of those atoms in space.
Model 1 (cis stereoisomer)
Model 2 (trans stereoisomer)
IUPAC Name:
IUPAC Name:
Transcribed Image Text:B. Cycloalkanes 1) Construct a model of the cyclic alkane: cyclopentane (C5H₁0). Because the five carbon atoms are locked in a ring, rotation about the single bonds is restricted; the plane of the ring a fixed geometry within the molecule. Toggle between full Lewis structures and skeletal structures by clicking the C-H tool. Model 1: Use the solid wedge tool to attach a methyl group to each of two different carbon atoms in the cyclopentane. Note the five carbons of the ring are in the plane of the paper, and the solid wedge indicates both methyls project forward, in front of the plane of the paper. Model 2: Use the solid wedge tool to attach first methyl group to one of two different carbon atoms in the cyclopentane, and use the dashed wedge tool to attach the second. Note the solid wedge indicates that one methyl projects forward, in front of the plane of the paper. The dashed wedge indicates the other methyl extends back, behind the plane of the paper. Click the broom to tidy up the structures; convert each to a three-dimensional ball-and-stick model by clicking the 2D to 3D tool. Take a screen prints of your MolView structures, showing both the Lewis structure and 3D model. 2) Draw a condensed structure for each of the two models that you build. That is, draw a five-membered ring to represent the cyclopentane, and use CH3- groups to represent the two methyl substituents. Make certain that your structures clearly illustrate the arrangement of the methyl substituents with respect to the fixed geometry of the cyclopentane ring. Write the IUPAC name for each structure, keeping in mind that the name should specifically describe not only the number of each type of atom and how they are connected, but also the arrangement of those atoms in space. Model 1 (cis stereoisomer) Model 2 (trans stereoisomer) IUPAC Name: IUPAC Name:
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 3 steps with 5 images

Blurred answer
Knowledge Booster
Alkanes and Cycloalkanes
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY