![Identify the indicated faces of carbon atoms in the following molecule as Re or Si. | Homework.Study.com Identify the indicated faces of carbon atoms in the following molecule as Re or Si. | Homework.Study.com](https://homework.study.com/cimages/multimages/16/screenshot_2022-07-20_at_10.20.43_pm1806269615368420155.png)
Identify the indicated faces of carbon atoms in the following molecule as Re or Si. | Homework.Study.com
![organic chemistry - Reduction of acetaldehyde from rectus and sinister faces - Chemistry Stack Exchange organic chemistry - Reduction of acetaldehyde from rectus and sinister faces - Chemistry Stack Exchange](https://i.stack.imgur.com/vs71f.jpg)
organic chemistry - Reduction of acetaldehyde from rectus and sinister faces - Chemistry Stack Exchange
![SOLVED: Identify the indicated faces in the following molecules as Re or Si top face COzH HOzC H;c CH; bottom face Oh A = Re 8 = Si A =Si B = SOLVED: Identify the indicated faces in the following molecules as Re or Si top face COzH HOzC H;c CH; bottom face Oh A = Re 8 = Si A =Si B =](https://cdn.numerade.com/ask_images/b248566d72a54036a40850032f2fb413.jpg)
SOLVED: Identify the indicated faces in the following molecules as Re or Si top face COzH HOzC H;c CH; bottom face Oh A = Re 8 = Si A =Si B =
![Scheme 2. Stereoselective hydride addition on the re or si face of 2+... | Download Scientific Diagram Scheme 2. Stereoselective hydride addition on the re or si face of 2+... | Download Scientific Diagram](https://www.researchgate.net/publication/295685822/figure/fig9/AS:342356252479493@1458635499269/Scheme2-Stereoselective-hydride-addition-on-the-re-or-si-face-of-2-M-configuration.png)
Scheme 2. Stereoselective hydride addition on the re or si face of 2+... | Download Scientific Diagram
![Internal chirality descriptors iR and iS and ire and isi. A proposed notation to extend the usefulness of the R/S system by retaining the sense of stereochemistry in cases of ligand ranking Internal chirality descriptors iR and iS and ire and isi. A proposed notation to extend the usefulness of the R/S system by retaining the sense of stereochemistry in cases of ligand ranking](https://onlinelibrary.wiley.com/cms/asset/86be0f12-8c10-4928-a349-cb18ad0592bf/chir22982-fig-0011-m.jpg)