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- The diaxial conformation of cis-1, 3-dimethylcyclohexane is approximately 23 kJ/mol (5.4 kcal/mol) less stable than the diequatorial conformation. Draw the two possible chair conformations, and suggest a reason for the large energy difference.myo-Inositol, one of the isomers of 1,2,3,4,5,6-hexahydroxycyclohexane, acts as a growth factor in both animals and microorganisms. Draw the most stable chair conformation of myo-inositol.Consider 1-bromo-2-methylpropane and draw the following. (a) The staggered conformation(s) of lowest energy (b) The staggered conformation(s) of highest energy
- Draw the lowest energy conformation of the following molecule along C2-C3. : OH 3 : ОНBased on the given planar structure of 1,2,3-trichloro-4-methylcyclohexane, which of the following structures corresponds to the most stable chair conformation of the compound (Figure below)? CI 'CI CI CI CI CH3CI CI H3CZ CI CI CI H3CZ il CI CI CH3CIWhich of the following conformers of isobutyl chloride is the most stable?
- In the most stable chair conformation of the cyclohexane below, how many methyl groups would be axial? H3C O one all three zero two CH3 CH3In the highest energy conformation of the compound below, how many methyl substituents are equatorial? CH3 CH3 H,CWhich of the following is an accurate conformational drawing for compound Z? Z