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The steric strain between the two terminal methyl groups accounts for the difference in energy between the two similar, yet very different conformations ...
Van der Waals strain is strain resulting from Van der Waals repulsion when two substituents in a molecule approach each other with a distance less than the sum of their Van der Waals radii. Van der Waals strain is also called Van der Waals repulsion and is related to steric hindrance . [ 1 ]
The interaction between the two flagpole hydrogens, in particular, generates steric strain. Torsional strain also exists between the C2–C3 and C5–C6 bonds (carbon number 1 is one of the two on a mirror plane), which are eclipsed — that is, these two bonds are parallel one to the other across a mirror plane. Because of this strain, the ...
a torsion angle between 90° and 150° or −90° and −150° is called anticlinal (ac) a torsion angle between ±150° and 180° is called antiperiplanar (ap), also called anti-or trans-conformation; Torsional strain or "Pitzer strain" refers to resistance to twisting about a bond.
Steric hindrance is often exploited to control selectivity, such as slowing unwanted side-reactions. Steric hindrance between adjacent groups can also affect torsional bond angles. Steric hindrance is responsible for the observed shape of rotaxanes and the low rates of racemization of 2,2'-disubstituted biphenyl and binaphthyl derivatives.
Ring strain theory was first developed by German chemist Adolf von Bayer in 1890. Previously, the only bonds believed to exist were torsional and steric; however, Bayer's theory became based on the interactions between the two strains. Bayer's theory was based on the assumption that ringed compounds were flat.
Stress and strain can be applied via torsional or axial analyzers. Torsional analyzers are mainly used for liquids or melts but can also be implemented for some solid samples since the force is applied in a twisting motion. The instrument can do creep-recovery, stress–relaxation, and stress–strain experiments.
However, because context will have an effect on steric interactions [7] some E s values can be larger or smaller than expected. For example, the value for phenyl is much larger than that for tert-butyl. When comparing these groups using another measure of steric bulk, axial strain values, the tert-butyl group is larger. [8]