Tasks point of view CI Figure 2: Confomational analysis 1. Draw all Newman projections of staggered conformations of the molecule in Figure 2 from the indicated point of view. 2. Select the lowest energy conformation and briefly explain your choice. 3. Boat conformation of cyclohexane does not experience ring strain. Nevertheless it is significantly less stable than the chair conformation. There are two types of strain that cause it. One is flagpole interactions. What is the second reason for higher energy of the boat conformation of cyclohexane? Drawing must be used as part of your answer.

Tasks point of view CI Figure 2: Confomational analysis 1. Draw all Newman projections of staggered conformations of the molecule in Figure 2 from the indicated point of view. 2. Select the lowest energy conformation and briefly explain your choice. 3. Boat conformation of cyclohexane does not experience ring strain. Nevertheless it is significantly less stable than the chair conformation. There are two types of strain that cause it. One is flagpole interactions. What is the second reason for higher energy of the boat conformation of cyclohexane? Drawing must be used as part of your answer.

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...

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Draw both chair conformations of the six membered rings below and circle the lowest energy conformation. If they are equal in energy circle both structures. Draw out all of the H atoms on your chair structure and clearly indicate the directionality for all of the H and non-H substituents.
req Zreq 2req 2req 2req [Review Topics) [References] Cyclohexane derivatives exist primarily in the most stable of the available chair conformations. Give the position, axial or equatorial, of each of the three groups shown when the ring is in the most stable chair conformation. If a group divides its time equally between axial and equatorial positions, indicate this with ax/eq. The table of "Axial Strain Energies for Monosubstituted Cyclohexanes" found in the "Strain Energy Increments" section of the Reference tool is useful for answering this question. OH HC Group a is Group bis Group cis Submit Answer OH b Retry Entire Group 9 more group attempts remaining o O · 9020 0
cyclohexane chair and boat conformation
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Use flat representation of rings, not chair in the drawing. Determine the most and least stable. Consider the most stable chair for each of these isomers, and then draw the most stable and least stable isomer based on a comparison of the best chair for each one.
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5.Draw the most stable conformer of each of the following ) Use Newman projections for straight chain compound and chair for cyclic compounds (а) 2,3-dimethylbutane (b) (c) .. |