Trans 1 3 Dimethylcyclohexane Chair Conformation
Trans 1 3 Dimethylcyclohexane Chair Conformation. When a substitutent is present at axial. The correct option is c.
In chair conformation of cyclohexane we have two position in the conformer. A similar conformational analysis can be made for the cis and trans stereoisomers of 1,3. Alternate axial and equatorial bonds of the adjacent carbons are cis to each other, that is, all the bonds facing.
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The chair conformation of cyclohexane comprises of axial and equatorial bonds. Answered may 15, 2019 by sweety01 (70.3k points) selected may 17, 2019 by vikash kumar. There are two possibilities that are cis or trans, but the position of the methyl group on axial or equatorial bond on cyclohexane determines whether the compound is cis or trans.
In Chair Conformation Of Cyclohexane We Have Two Position In The Conformer.
Alternate axial and equatorial bonds of the adjacent carbons are cis to each other, that is, all the bonds facing. The conformation in which the both the methyl groups are on the equatorial position will be. The correct option is c.
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When a substitutent is present at axial. A similar conformational analysis can be made for the cis and trans stereoisomers of 1,3. A similar conformational analysis can be made for the cis and trans stereoisomers of 1,3.
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