1-conctruct trans-1,2-dimethylcyclohexane.by means of ring flips, examine the model with the two-CH3 groups axial and the...

1-conctruct trans-1,2-dimethylcyclohexane.by means of ring flips, examine the model with the two-CH3 groups axial and the two -CH3 groups equatorial (e,e=equatorial,equatorial a,a=axial, axial) wich is more stable conformation ? explain the answer.

Need part 2 of this

2-construct cis-1,2-dimethylcyclohexane by placing one-CH3 group axial and the other equatorial (a,e=axial, equatorial,e,a=equatorial,axial)Do rings flips and examine the 2 chair conformations. ( Explain wich is more stable)give the 2 isomers , trans-1-2-dimethylcyclohexane and cis-1,2-dimethycyclohexane, which is more stable isomers . Explain your answer.

Expert Solution

Note: both the cis conformers are equally stable whereas the equitorially substituted trans conformer is the most stable among all given conformers.

queen_honey_blossom answered 1 year ago

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