The following compounds are stereoisomers. Rank in order of increasing the stability (the least stable to the most stable.) CI CI CI CI A. B. C. D. SUBSTITUENT 1,3-DIAXIAL INTERACTIONS (KJ/MOL) EQUATORIAL-AXIAL RATIO (AT EQUILIBRIUM) Which of the following is the most stable chair conformation of the following cyclohexane? . B. C. D. E OH OH HO OH Et So anOC a La aa a oH C SUBSTITUENT 1,3-DIAXIAL INTERACTIONS (KVMOU) EQUATORIAL-AXIAL RATIO (AT EQUILIBRIUM) 70. 30 ci 2.0 -OH 4.2 83: 17 95.5 7.6 -CH, -CH2CH3 -CH(CH3)2 8.0 964 92 97: 3 999911 Classify each pair of compounds as constitutional isomers, diasteromers, enantiomers, identical molecules. and , , b. and OK Answer Answer for a diasteromers A Answer for b constitutional isomers identical enantiomers B enantiomers identical diasteromers D enantiomers constitutional F enentiomers