24 сент. 2022 г. · The most stable conformation will be the one with the bulkiest substituent in the equatorial position. Steric bulk decreases in the order tert-butyl > ...

13 окт. 2011 г. · Since Br is a bigger atom than Cl, bromine takes the equatorial position while chlorine takes the axial position. Axial vs. Equatorial - CHEMISTRY COMMUNITY How to determine higher stability - CHEMISTRY COMMUNITY Cis and Trans and Stability - CHEMISTRY COMMUNITY Chlorine and Bromide substituents axial or equatorial? Другие результаты с сайта lavelle.chem.ucla.edu

24 сент. 2022 г. · Although the conformation which places the methyl group in the equatorial position is more stable by 7 kJ/mol, the energy provided by ambient ...

17 окт. 2024 г. · Equatorial substituents, on the other hand, experience much less steric strain. They point out, away from other substituents, minimizing the ...

27 июн. 2014 г. · In other words, the equatorial conformer is more stable by 1.70 kcal/mol. Since there are two gauche interactions, and the strain energy is 1. ...

12 дек. 2013 г. · The two chair conformations have the lowest total energy, and are therefore the most stable. Since cyclohexane's planar form results into bond ...

14 окт. 2024 г. · One of the main factors determining stability is the 1,3-diaxial interaction. This occurs when two axial substituents on the same side of the ...

For mono-substituted cyclohexane, the equatorial-conformer is more stable than the axial-conformer because of the 1,3-diaxal interaction.

17 июл. 2022 г. · Also, Equatorial methylcyclohexane has less energy than that of axial Methylcyclohexane, which offers extra stability to the former one.

3 июн. 2022 г. · Generally , equatorial conformers are more stable due to less torsional strain . However in this case , where the ring is di-subsituted at ...