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  • https://chem.libretexts.org/Workbench/Chemistry_LHS_Bridge/16%3A_Chirality/16.09%3A_Stereoisomers/16.9.11%3A_Stereoisomerism_in_Disubstituted_Cyclohexanes
    The 1,1-dichloro isomer is omitted because it is an unexceptional constitutional isomer of the others, and has no centers of chirality (asymmetric carbon atoms). The diequatorial conformer predominate...The 1,1-dichloro isomer is omitted because it is an unexceptional constitutional isomer of the others, and has no centers of chirality (asymmetric carbon atoms). The diequatorial conformer predominates in each case, the (R,R) conformations being mirror images of the (S,S) conformations. All the chair conformers of these isomers are achiral, and the diequatorial conformer of the trans isomer is the predominate species at equilibrium.

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