Abstract
The QTAIM trajectories were calculated to locate the chirality-helicity equivalence for the S and R stereoisomers of lactic acid and alanine that were recently located using the stress tensor trajectories. The QTAIM trajectories were defined by the variation of the position of the torsional bond critical point (BCP) upon a structural change, along the torsion angle θ, involving a chiral carbon atom. The QTAIM trajectories and BCP shifts provided weak and good agreement with the naming schemes from optical experiment respectively. The analysis was applied to achiral glycine and the implications of the torsional directional preferences found are discussed.
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