In this example, both Br\'s are in the equatorial position. In a 1, 4-disubstitu

Question

In this example, both Br's are in the equatorial position. In a 1, 4-disubstituted cyclohexane, trans-substitution results in either two axial groups (less favored energetically) or two equatorial groups (more favored energetically). Identify the cis-, trans- relationship of the two groups, and identify the axial/equatorial nature of the groups. More than one answer must be indicated for full credit for this question. One bromine atom is in an axial conformation, while the other bromine atom is in an equatorial conformation. Both bromine atoms are in an equatorial conformation This compound should be properly called cis-1, 4-dibromocyclohexane. This compound should be properly called trans-1, 4-dibromocyclohexa Both bromine atoms are in an axial conformation.

Explanation / Answer

this compound should be properly called trans 1 4 di bromocyclohexane

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