The cyclohexane derivative shown exists primarily in the more stable of the two available chair conformations. Give the position, axial or equatorial,of each of the three groups shown in the more stable chair conformation. If a group divides its time equally between axial and equatorial positions,indicate this with ax/eqReview Topios]References]The table of "Axial Strain Energies for Monosubstituted Cyclohexanes" found in the "Strain Energy Increments" section of the Reference tooluseful for answering this question.H cCH3NCGroup a isGroup b isGroup c is9 more group attempts remainingRetry Entire GroupuமாlAnswerNextPreviousSeve and Ex11:5810/22/

The given conformation is drawn as two chair confirmations as,

Answered: The cyclohexane derivative shown exists…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter7: Cycloalkanes

Section: Chapter Questions

Problem 17E: Build a model of methylcyclohexane, and use the model to complete the following Newmanprojections of...

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The cyclohexane derivative shown exists primarily in the more stable of the two available chair conformations. Give the position, axial or equatorial, of each of the three groups shown in the more 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. For compounds 1 and 2
The highest energy conformation of ethane has 12 kJ/mol of strain. The two highest conformations of butane have 16 and 19 kJ/mol of strain, respectively. How much strain does the highest energy conformation of 2,3-dimethylbutane have?
Between the cis and trans configuration of 1-chloro-4-methylcyclohexane, which is the most stable stereoisomer and configuration? To prove your argument, draw a model or use a modeling software to model cis- and trans-1-chloro-4-methylcyclohexane (show all the hydrogens and ensure proper chair conformation) and use arrows to show where steric strain occurs.
For the 1,2-dichlorocyclohexane stereoisomers, which conformation of the trans stereoisomer has the lower energy, the diaxial or the diequatorial conformer? Which isomer and conformation of the three you built has the lowest energy? E of all the isomers of 1,2-dichlorocyclohexane. Explain the differences in energy, i.e., identify the sources of strain in the conformations you built. Show the sources of strain in a drawing.
Between the cis and trans configuration of 1-chloro-3-methylcyclohexane, which is the most stable stereoisomer and configuration? To prove your argument, use your models or a modelling software to model cis- and trans-1-chloro-3-methylcyclohexane (show all the hydrogens and ensure proper chair conformation) and use arrows to show where steric strain occurs. Include these photos in your answer.
Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Long and detailed explanations are not needed. Keep it short, brief, and direct because I only need the answers as soon as possible. Calculate the total strain energy in each of the two chair conformations of cis-1-tert-butyl-4-chlorocyclohexane. By how much energy is the more stable conformation favored (this is the difference in energy between the two conformations)? NOTE: The strain energy for one H,Cl interaction is 1.0 kJ/mol while for H,-C(CH3)3 (t-butyl) is 11.4 kJ/mol.
Draw the most stable conformation of the molecule while taking into account the approximate values of the energies of the following skew interactions:
calculate the amount of steric strain in each of the chair conformers of 1,1,3-trimethylcyclohexane. Which conformer predominates at equilibrium?
Which is the most stable stereoisomer and configuration of 1-chloro-4-methylcyclohexane between the cis and trans configurations? Please explain. Provide chair structures + show all H for cis- and trans-1-chloro-4-methylcyclohexane, and use arrows to show where steric strain occurs.
Explain the equitorial and axial orientation of the substituents in the more stable forms of the cis and trans isomers of 1-isobutyl-2-methylcyclohexane. Be sure to discuss strain and energy in relation to conformations.
Draw the two chair conformations of 1,1,3-trimethylcyclohexan ,and estimate the amount of strain energy in each. Which conformation is favored
Which conformation of cyclohexane has the greater steric strain?

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