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Topic: CIP - R/S nomenclature for L-cysteine and L-serine  (Read 2585 times)

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Offline DoStateStuff

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CIP - R/S nomenclature for L-cysteine and L-serine
« on: May 30, 2016, 08:32:01 AM »
I've got a question that asks why the CIP R/S nomenclature for L-cysteine is opposite to that for L-serine. I can't for the life of me figure out what this question is asking?

Any help appreciated!

Offline sjb

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Re: CIP - R/S nomenclature for L-cysteine and L-serine
« Reply #1 on: May 30, 2016, 08:41:58 AM »
I've got a question that asks why the CIP R/S nomenclature for L-cysteine is opposite to that for L-serine. I can't for the life of me figure out what this question is asking?

Any help appreciated!

What are the relevant structures?

Offline DoStateStuff

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Re: CIP - R/S nomenclature for L-cysteine and L-serine
« Reply #2 on: May 30, 2016, 09:25:04 AM »
What are the relevant structures?

It asks to draw the three-dimensional structural enantiomers of L-cysteine (C3H7NO2S) and L-serine (C3H7NO3), and then the question above; why the R/S nomenclature is opposite

Offline kriggy

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Re: CIP - R/S nomenclature for L-cysteine and L-serine
« Reply #3 on: May 30, 2016, 09:52:31 AM »
Well
a) what are the structures?
b) what are the CIP priorities in those compounds?

Offline Babcock_Hall

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Re: CIP - R/S nomenclature for L-cysteine and L-serine
« Reply #4 on: May 30, 2016, 05:57:08 PM »
This is an interesting question that illustrates why the D,L system is more useful for the amino acids than the R,S system is, in one respect.

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