Draw the structural isomers of C2H4BrCl and identify which of them has a chiral center. Then, create the Newman projection of the most stable conformational isomer and indicate its absolute configuration.
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Draw the structural isomers of C2H4BrCl and identify which of them has a chiral center. Then, create the Newman projection of the most stable conformational isomer and indicate its absolute configuration.
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- If you rotate the hydrogen atoms to a different position in a a model of C2H6 by turning about the central C—C bond, do you get different structural (or constitutional) isomers of C2H5Cl?Why are these two conformational isomers? I was under the impression that in molecules with only sigma bonds, the bonds can rotate freely, and so the placement of the chlorines wouldn't matter?Draw the skeletal structures of all isomers of C₆H₁₂ that have the (E)-configuration.
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