Consider the chair conformation below :CH,When the chair flips:One methyl group becomes axial, the other methyl group equatorial and the bromine becomes equatorial.The bromine atom becomes equatorial and methyl groups axialAll groups become axialThe bromine atom becomes axial and the methyl groups become equatorial.

Please find the answer attached here

Consider the chair conformation below: CH, When the chair fips: One methyl group becomes axial, the other methyl group equatorial and the bromine becomes equatorial. B The bromine atom becomes equatorial and methyl groups axial All groups become axial The bromine atom becomes axial and the methyl groups become equatorial.

Consider the chair conformation below: CH, When the chair fips: One methyl group becomes axial, the other methyl group equatorial and the bromine becomes equatorial. B The bromine atom becomes equatorial and methyl groups axial All groups become axial The bromine atom becomes axial and the methyl groups become equatorial.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter2: Alkanes And Cycloalkanes

Section2.5: Conformations Of Alkanes And Cycloalkanes

Problem 2.9P: Following is a chair conformation of cyclohexane with the carbon atoms numbered 1 through 6. (a)...

See similar textbooks

Similar questions

Following is a planar hexagon representation for one isomer of 1,2,4-trimethylcyclohexane. Draw the alternative chair conformations of this compound and state which of the two is more stable.
Following is a chair conformation of cyclohexane with the carbon atoms numbered 1 through 6. (a) Draw hydrogen atoms that are above the plane of the ring on carbons 1 and 2 and below the plane of the ring on carbon 4. (b) Which of these hydrogens are equatorial? Which are axial? (c) Draw the alternative chair conformation. Which hydrogens are equatorial? Which are axial? Which are above the plane of the ring? Which are below it?
myo-Inositol, one of the isomers of 1,2,3,4,5,6-hexahydroxycyclohexane, acts as a growth factor in both animals and microorganisms. Draw the most stable chair conformation of myo-inositol.
Use your answers from Problem 2.48 to complete the table showing correlations between cis,trans and axial,equatorial for disubstituted derivatives of cyclohexane. Draw the alternative chair conformations for the cis and trans isomers of 1,2-dimethylcyclohexane, 1,3-dimethylcyclohexane, 1,4-dimethylcyclohexane. (a) Indicate by a label whether each methyl group is axial or equatorial.
Draw a chair conformation of 1,4-dimethylcyclohexane in which one methyl group is equatorial and the other is axial. Draw the alternative chair conformation and calculate the ratio of the two conformations at 25C.
Can you draw the chair conformation of trans 1 methyl 2 chlorocyclohexane
Draw the alternative chair conformations for the cis and trans isomers of 1,2-dimethylcyclohexane, 1,3-dimethylcyclohexane, and 1,4-dimethylcyclohexane. Q.) Indicate by a label whether each methyl group is axial or equatorial.
Draw the alternative chair conformations for the cis and trans isomers of 1,2-dimethylcyclohexane, 1,3-dimethylcyclohexane, and 1,4-dimethylcyclohexane. Q.) For which isomer(s) is one chair conformation more stable than the other?
Draw the two chair conformations of cis-1,3-dimethylcyclohexane, and label all the positions as axial or equatorial.
The majority of cis-3-isopropyl-1-methylcyclohexane molecules assume a conformation wherein a. both isopropyl and methyl groups are equatorial. b. the methyl group is axial and the isopropyl group is equatorial. c. the isopropyl group is axial and the methyl group is equatorial. d. both isopropyl and methyl groups are axial.
The molecule cis-1-bromo-4-isopropylcyclohexane can exist in two different chair conformations, which are interconvertible by means of a ring flip. Draw the most stable conformer.
Looking alongC1−C2andC4−C5bonds, draw a Newman projection for each of the two chair conformations of trans 1,2-dimethylcyclohexane.