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What is the overall stability of carbanion? Why is phenyl carbanion less stable than cyclopropene carbanion? Are they both resonating?
![SOLVED: If both conformations of the isomer are equally stable, select both. Select the more stable conformation of cis-1,2-di(2-methylpropyl)cyclohexane. D Select the more stable conformation of trans-1 2-di(2-methylpropyl)cyclohexane continued below ... SOLVED: If both conformations of the isomer are equally stable, select both. Select the more stable conformation of cis-1,2-di(2-methylpropyl)cyclohexane. D Select the more stable conformation of trans-1 2-di(2-methylpropyl)cyclohexane continued below ...](https://cdn.numerade.com/ask_images/2c336ef6c79645abb7fb0c5d60e7d453.jpg)
SOLVED: If both conformations of the isomer are equally stable, select both. Select the more stable conformation of cis-1,2-di(2-methylpropyl)cyclohexane. D Select the more stable conformation of trans-1 2-di(2-methylpropyl)cyclohexane continued below ...
![Result Summary Graph for Netflow v5 Above figure show the overall graph... | Download Scientific Diagram Result Summary Graph for Netflow v5 Above figure show the overall graph... | Download Scientific Diagram](https://www.researchgate.net/publication/4376565/figure/fig1/AS:340839344689155@1458273840250/Result-Summary-Graph-for-Netflow-v5-Above-figure-show-the-overall-graph-for-Netflow-v5.png)
Result Summary Graph for Netflow v5 Above figure show the overall graph... | Download Scientific Diagram
![I am confused about this answer explanation? If we use ARIO to determine base stability, shouldn't hydroxide be the more stable base since a negative charge is more stable on an O I am confused about this answer explanation? If we use ARIO to determine base stability, shouldn't hydroxide be the more stable base since a negative charge is more stable on an O](https://preview.redd.it/5d7rivkbowe51.jpg?auto=webp&s=881afed9c5a23f79cdee14280ba519cc66e6eb37)