Stereoisomerism has been a subject of fundamental interest for quite a long time due to the spatial geometry between atoms in a molecule and their sizeable role in the fields of pharmacology, atmospheric, and astrochemistry. To study this nature, we propose a method that takes advantage of the ‘universality in fragmentation’ as a scientific framework to disentangle structural dynamics in molecules. For the first time, we experimentally visualized the chiral and diastereomeric nature of H2O2 through the reconstruction of H_2 O_2^(n+) (n=3-5) dissociation dynamics, besides concerted or sequential breakup channels. We also demonstrated the homochirality in H2O2 from the deduced enantiomeric excess, 4.486±0.9502%. Unlike ultrafast or time-resolved studies, we here established that recoil-ion momentum spectrometer (RIMS) in combination with post-coulomb explosion imaging methodologies is the most reliable route to unravel the real-time structure of a molecule irrespective of any probe, as it relies on a momentum-correlation picture.