![Given cyclohexane in a chair conformation, substitute two of the H labels with bromine and chlorine to construct the more stable conformation of cis-1-bromo-3-chlorocyclohexane. Use the numbering prov | Study.com Given cyclohexane in a chair conformation, substitute two of the H labels with bromine and chlorine to construct the more stable conformation of cis-1-bromo-3-chlorocyclohexane. Use the numbering prov | Study.com](https://study.com/cimages/multimages/16/jghjhghgjh4555585643924876139.png)
Given cyclohexane in a chair conformation, substitute two of the H labels with bromine and chlorine to construct the more stable conformation of cis-1-bromo-3-chlorocyclohexane. Use the numbering prov | Study.com
![Stereoisomeric Conformations, Different Perspectives, Achiral Stereoisomers and Meso Compounds | Organic Chemistry Solutions Stereoisomeric Conformations, Different Perspectives, Achiral Stereoisomers and Meso Compounds | Organic Chemistry Solutions](http://organicchemistrysolutions.com/wp-content/uploads/2013/11/OCS-Chirality-Confusions-Conformations.png)
Stereoisomeric Conformations, Different Perspectives, Achiral Stereoisomers and Meso Compounds | Organic Chemistry Solutions
![I'm learning about the chair conformation of cyclohexane compounds. I am still not 100% on it. I know that II is a correct chair conformation for I, but is III also an I'm learning about the chair conformation of cyclohexane compounds. I am still not 100% on it. I know that II is a correct chair conformation for I, but is III also an](https://preview.redd.it/ck68b69vato51.jpg?width=640&crop=smart&auto=webp&s=d34670e4c4ad884ea1ca6fe3f36e113d9781d981)