emitted_echo
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- TL;DR
- How did we first discover that a racemic mixture had two different chiral compounds when it behaves the same as an achiral compound.
Lately, I've been doing a lot of research on chirality in biochemical and medical contexts; especially from a developmental standpoint. I am aware of how each enantiomer behaves differently from its corresponding mirror-image molecule, but i'm confused by racemic mixtures. I understand on a conceptual level that it's just a mixture between 'right-handed' and 'left-handed' chiralities, but how was this discovered? Everything I have read says that racemic mixtures behave identically to achiral ones since the two essentially cancel out the other's optical properties, so does this mean that there is a chance other compounds we believed to be achiral could simply be racemic mixtures we haven't separated, or is there something I am missing? Additionally, I am aware that it is incredibly complicated to separate them at times- especially depending on what specifically you're working with,- so how were these processes chosen?
Thank you in advance for any responses. I am very new to research on this subject, so any and all help is appreciated.
Thank you in advance for any responses. I am very new to research on this subject, so any and all help is appreciated.