iven the planar trisubstituted cyclohexane, fill in the missing substituents (with h or cl ) to complete the two possible cyclohexane chair conformations. then, determine the more stable conformer. you might find it helpful to make a model of the cyclohexane to help visualize the chair conformations. a cyclohexane ring with three substituents, all on wedged bonds. moving around the ring counter clockwise, there is a bromine on carbon 1, a fluorine on carbon 2 and a chlorine on carbon 3. you are currently in a labeling module. turn off browse mode or quick nav, tab to items, space or enter to pick up, tab to move, space or enter to drop. chair 1 has the leftmost carbon pointing down and the rightmost carbon pointing up. arbitrarily numbering the leftmost carbon as 1 and moving clockwise, bin 1 is the equatorial bond on carbon 3, bin 2 is the axial bond on carbon 4, bin 3 is the equatorial bond on carbon 4, bin 4 is the equatorial bond on carbon 5 and bin 5 is the axial bond on carbon 5. chair 2 has the leftmost carbon pointing up and the rightmost carbon pointing down. arbitrarily numbering the leftmost carbon as 1 and moving clockwise, bin 6 is the axial bond on carbon 3, bin 7 is the equatorial bond on carbon 3, bin 8 is the equatorial bond on carbon 4, bin 9 is the axial bond on carbon 4, bin 10 is the axial bond on carbon 5 and bin 11 is the equatorial carbon on carbon 5. the axial and equatorial positions not specified are all hydrogens answer bank which is the more stable conformer? chair 2 chair 1