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We theoretically introduce a scheme to perform Ramsey spectroscopy on aracemic mixture of chiral molecules, simultaneously extracting the transitionfrequencies of the left- and right-handed molecules, known as enantiomers. Bytaking the difference between the enantio-specific frequencies, we isolate theweak force parity violation (PV) shift, which is predicted to break thesymmetry between enantiomers. To perform the scheme, we design a pulse sequencethat creates enantio-specific superpositions in a three-level system using theenantiomer-dependent sign of the electric-dipole moment components' tripleproduct. A delayed second pulse sequence completes the Ramsey interrogationsequence, enabling readout of the phase evolution for each enantiomer'stransition through a separate quantum state. Our technique overcomes the needto alternate between enantio-pure samples to measure PV. We describe theadvantages of the proposed method for precision metrology.

Simultaneous Enantiomer-Resolved Ramsey Spectroscopy Scheme for Chiral Molecules