For cis-1,3-dimethylcyclohexane, which structures represent the possible boat conformations?
Cyclohexane can exist in three stable conformations. They are chair, boat and twist boat. Among the three conformations, chair conformation is most stable. In boat conformation of cyclohexane, two types of groups are present at each carbon atom. They are axial groups and equatorial groups. We should identify the cis conformations from the given boat conformations.
If two substituents are cis to each other then they are in up, up (or) down, down to each other in boat conformation.
If two substituents are trans to each other then they are in up, down (or) down, up to each other in boat conformation.
The given boat conformations are,
The possible boat conformations for the given cis-1,3-dimethylcyclohexane are,
Ans:Thus, the possible boat conformations of cis-1,3-dimethylcyclohexane are,
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For cis-1,3-dimethylcyclohexane, which structures represent the possible boat conformations?
plz explain Which of the following structures represent conformations that can be adopted by trans-1,2-dimethylcyclohexane? (Indicate all that apply) B E Which of the following structures represent conformations that can be adopted by cis-1,2-dimethylcyclohexane? (select all that apply) A B D E
11. Build the chair and boat conformations and identify the most stable conformation. Identify the 1,3-diaxial interactions. 12. Draw the most stable conformation of (a) ethylcyclohexane (b) 3-isopropyl-1,1-dimethylcyclohexane (c) cis-1-tert-butyl-4-isopropylcyclohexane 13. Draw all possible conformations of 1,4-dimethylcyclohexane and identify the most stable conformation 14. (a) Draw both chair conformations of cis-1,2-dimethylcyclohexane, and determine which conformer is more stable. (b) Repeat for the trans isomer. (c) Predict which isomer (cis or trans) is more stable. 15. (a) Draw both chair conformations...
Draw the 2 chair conformations, in the chair format, of cis-1,3-dimethylcyclohexane. Label which one is the least stable and which is the most stable. If they are of equal stability, clearly state that they are of equal stability.
For cis-1,3-dimethylcyclohexane, which two chair conformations are in equilibrium?
Which of the statements below correctly describes the chair conformations of cis–1,3–dimethylcyclohexane? a. The two chair conformations are of equal energy. b. The higher energy chair conformation (least stable) contains one axial methyl group and one equatorial methyl group c. The lower energy chair conformation (most stable) contains one axial methyl group and one equatorial methyl group d. The higher energy chair conformation (least stable) contains two axial methyl groups Please show work for the correct answer.
rank cis-1,2-dimethylcyclohexane, cis-1,3-dimethylcyclohexane and cis-1,4-dimethylcyclohexane in increasing order of stability.
Please make hand writing neat. Thank you:) 12. Construct cis-1,3-dimethylcyclohexane by placing both -CH, groups in the axial Which is the more positions. Do ring flips and examine the two chair conformations. stable conformation? Explain your answer (12) 13. Construet trans-1,3-dimethylcyclohexane by placin g one- CH3 group axial and the other equatorial. Do ring flips and examine the two chair conformations. the more stable conformation? Explain your answer (13a). Given the two1 trans-1,3-dimethylcyclohexane and cis-1,3-dimethyleyc stable isomer? Explain your answer...
Draw the Newman structures for 1,2 dimethycyclohexane , 1,3 dimethylcyclohexane and 1,4 dimethylcyclohexane. Please draw the cis and trans for each. thank you
6. Build the cyclobutane ring and study the angle strain and torsional strain. Draw the structures to explain these factors. 7. The conformation of cyclobutane is slightly folded. Folding gives partial relief from the eclipsing of bonds, as shown in the Newman projection. Compare this actual structure with the hypothetical planar structure. Draw the relevant structures. 8. trans-1,2-Dimethylcyclobutane is more stable than cis-1,2-dimethylcyclobutane, but cis-1,3- dimethylcyclobutane is more stable than trans-1,3-dimethylcyclobutane. Use the molecular models to find the reasons for...
1,1 CH cis-1,3-dimethylcyclohexane