also chiral stationary phase reacts with both enantiomers, but with a different strenght of binding. Guy who is stronger interacting will come later, guy who is weaker interacting will come first, I think there is over statement in your video, nevertheless pretty good
@Moxormog10 жыл бұрын
I love you! This is going to help me on my orgo I exam :)
@bangladeshivloggeradventures3 ай бұрын
In this example, is the chiral stationary phase R?
@avirajsarkar584610 жыл бұрын
plz explain the apparatus in the experiment......
@kachingchan922810 жыл бұрын
thanks very much!!
@pharmedutainment7 жыл бұрын
What program is used to produce the drawing in concert with the discussion?
@wrednykocurek3 жыл бұрын
Not S or R conformation, configuration is the proper word
@pythongamer39457 ай бұрын
Right
@taylorclarke25505 жыл бұрын
Wouldnt the molecules at the beginning of the video be diastereomers not enatiomers because the configuration of one of their chiral centers is different?
@romainrabany82785 жыл бұрын
recall: diastereomers are not superimposable and not mirror images of each other. Enantiomers on the other hand are not superimposable; however, they are mirror images of each other. I think what you are mistaking with is what is called an epimer, where one chiral center differs in both molecules; however, epimers are a type of diastereomer and not an enantiomer of eachother. if you imagine putting one of the molecule in the beginning of the video in front of a mirror we would obtain the other molecule.
@trollmcclure18844 жыл бұрын
so there'S no easy way I can test my L-ascorbic acid without chiral stationary phase? That's what I thought
@creillyucla3 жыл бұрын
what do you mean by test? If you want to check whether or not it is racemic (equal parts L and R), you can measure it's optical activity (whether or not it rotates polarized light)