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  2. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    For example, butane has three conformers relating to its two methyl (CH 3) groups: two gauche conformers, which have the methyls ±60° apart and are enantiomeric, and an anti conformer, where the four carbon centres are coplanar and the substituents are 180° apart (refer to free energy diagram of butane).

  3. Eclipsed conformation - Wikipedia

    en.wikipedia.org/wiki/Eclipsed_conformation

    In the example of ethane, such a graph shows that rotation around the carbon-carbon bond is not entirely free but that an energy barrier exists. The ethane molecule in the eclipsed conformation is said to suffer from torsional strain, and by a rotation around the carbon carbon bond to the staggered conformation around 12.5 kJ/mol of torsional ...

  4. Osmoconformer - Wikipedia

    en.wikipedia.org/wiki/Osmoconformer

    The crab-eating frog, or Rana cancrivora, is an example of a vertebrate osmoconformer. The crab-eating frog also regulates its rates of urea retention and excretion, which allows them to survive and maintain their status as osmoconformers in a wide range of external salinities. [ 3 ]

  5. Stefan–Boltzmann law - Wikipedia

    en.wikipedia.org/wiki/Stefan–Boltzmann_law

    Stefan surmised that 1/3 of the energy flux from the Sun is absorbed by the Earth's atmosphere, so he took for the correct Sun's energy flux a value 3/2 times greater than Soret's value, namely 29 × 3/2 = 43.5. Precise measurements of atmospheric absorption were not made until 1888 and 1904. The temperature Stefan obtained was a median value ...

  6. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    For example, a t-butyl substituent would sustain a higher energy gauche interaction as compared to a methyl group, and therefore, contribute more to the instability of the molecule as a whole. In comparison, a staggered conformation is thus preferred; the larger groups would maintain the equatorial position and lower the energy of the entire ...

  7. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

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  9. Conformon - Wikipedia

    en.wikipedia.org/wiki/Conformon

    Therefore, conformons can be defined as packets of conformational energy generated from substrate binding or chemical reactions and confined within biopolymers. [ 1 ] On the other hand, from a physics standpoint, the conformon is a localization of elastic and electronic energy which may propagate in space with or without dissipation. [ 2 ]