3.Draw the most stable chair conformation for each of thefollowing compounds(a) Cis-1-ethyl-2-methyl cyclohexane(b) Trans-1-ethyl-2-methyl cyclohexane(c) Which one is more stable, a or b ?

Chair conformation of cyclohexane is more stable.

Answered: 3.Draw the most stable chair…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter7: Cycloalkanes

Section: Chapter Questions

Problem 12CTQ: Fill in the blanks: cis-1,3-Dimethylcyclohexane has two different chair conformations: one withboth...

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a model of cyclohexane in a chair conformation, and explain why the names “axial” and“equatorial’ are appropriate.
Fill in the blanks: cis-1,3-Dimethylcyclohexane has two different chair conformations: one withboth methyl groups in __________ positions and one with both methyl groups in ____________ positions.
A trisubstituted cyclohexane with three substituents-red, green, and blue-undergoes a ring-flip to its alternate chair conformation. Identify each substituent as axial or equatorial, and show the positions occupied by the three substituents in the ring-flipped form.
The diaxial conformation of cis-1, 3-dimethylcyclohexane is approximately 23 kJ/mol (5.4 kcal/mol) less stable than the diequatorial conformation. Draw the two possible chair conformations, and suggest a reason for the large energy difference.
Draw one chair conformer of (1S,2R,4R)-4-chloro-2-methylcyclohexan-1-ol. Include all groups of the three stereocenters, but no other hydrogens.
Draw the best chair conformation of trans 1-t-butyl-3-methylcyclohexane.
Draw the two chair conformations of each compound, and label the substituents as axial and equatorial of cis-1-ethyl-3-methylcyclohexane
Draw a newman projection of the given compound E viewed from C2-C3 oriented according to the first template. Then use the newman projection to demonstrate the most stable conformation around C2-C3 bond according to the second template
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Draw both chair conformations of cyclohexane. Label the axial hydrogens a and the equitoral hydrogens e.
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3.Draw the most stable chair conformation for each of the following compounds (a) Cis-1-ethyl-2-methyl cyclohexane (b) Trans-1-ethyl-2-methyl cyclohexane (c) Which one is more stable, a or b ?