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- 5. CIRCLE ALL THAT APPLY: Why is it so difficult to physically separate enantiomers from each other in a mixture? a. They are the same compound b. They have the same melting points c. They have the same densities d. They are both meso compoundsLocate the stereogenic centers in each compound. A molecule may have one or more stereogenic centers. Gabapentin enacarbil [part (d)] is used to treat seizures and certain types of chronic pain.Locate the stereogenic centers in attached compound. A molecule may have one or more stereogenic centers. Gabapentin enacarbil [part (d)] is used to treat seizures and certain types of chronic pain.
- Locate the stereogenic centers in attached molecule. Compounds may have one or more stereogenic centers.Part D. Do the two structures A and B of each pair drawn below represent the same molecule, constitutional isomers, or stereoisomers? If A and B are stereoisomers, further classify them as enantiomers or diastereomers. H3C Structure A H3C HO H3C H3C Br T H H3C H HO H3CC H C Br HC H H H H CH₂Br CH₂CH3 H CH₂CH3 CH₂OH OH H HO G G H HO H HO G CH3 CH3 CH3 Br Hallo H H3C H Structure B H3C CH3 Br WING H Br HOCH₂ CH3 CH3 HO H CH₂OH H CH₂CH3 H CH₂CH3 H H H H H H Gim CH3 H OH "H ·GII. CH3 HO. OH OH CH3 CH3 OH Relationship of A and BDraw the enantiomer of attached compound.
- 4. Do the following structures represent the same molecules or pairs of enantiomers? Additionally, convert the perspective structures to Fischer projections and vice versa. a. b. C. d. 11 CH HOH₂CH₂C-COH CH₂Br H₂C-CCI CH₂CH3 CH₂Br H-OH CH3 CI HỌC CHỊCH H CH₂CH3 CI HẠCH,C-C 'CH, CH₂Br H₂CH₂C-CH₂CH₂OH OH H HO-CH3 CH₂Br CH3 0-5-6-5 H+CI CH CH₂CH3Locate the stereogenic centers in each molecule. Compounds may have one or more stereogenic centers.Does methylcyclopentane have a stereogenic center?
