24 февр. 2017 г. · I know that my book considers a chair flip to result in a diastereomer because of the high energy barrier. The internet seems to ... |
6 дек. 2021 г. · No. It's the same molecule with the same stereochemistry. The ring flip is not an isomer, it's a conformer. |
1 окт. 2022 г. · The answer is A (identical compounds). This is confirmed by seeing that rotating the first structure counter clockwise 180 deg gives the second structure. |
19 окт. 2020 г. · No. Ring flip is just rotation of bonds. It didn't change configuration. It just changes conformer. Configuration is changed when molecule breaks bonds or ... |
6 янв. 2021 г. · The two chairs that can form are enantiomers. In the drawing shown, from the original structure, 1 is the enantiomer. 2 is identical to 1 ... |
10 апр. 2024 г. · It is enantiomers because, all groups in the asymmetrical carbons are inverted, the other molecule is a mirror image,If it were diastereomer, ... |
23 авг. 2020 г. · Enantiomers are stereoisomers that are non ... stereoisomers that interconvert by low energy processes like bond rotations and chair flips. |
12 июн. 2020 г. · In B, I did the same thing and found both of the stereocenters to change R / S configurationleading me to think that they are enantiomers. |
17 мар. 2024 г. · As drawn they arent enantiomers because they are the same molecules and are indistinguishable from each other. Take a simple chiral molecule ... |
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