My lecture notes describe epimers as compounds which differ by configuration at only one carbon and gives the example of D-erythrose and D-threose as being epimers.

However isn't that the same thing as diastereomers? My understanding is that epimers are supposed to be some kind of subset of diastereomers, however I am not sure how or why. I tried searching the web but I got more confused with one site saying that carbohydrates in open form can have two different chirality centres and still be epimers.


3 Answers 3


Relationship of stereoisomers

This scheme I just drew up specifically for you should answer your question.

Diastereomers are stereoisomers that are not enantiomers of each other. That includes conformers (geometric isomers that derive from single bond rotation; usually interconverting rapidly) and atropisomers (under which I would subsume E/Z isomers; they derive from hindered rotation around a typically single bond and are separable) and anything with differeces in asymmetric carbons.

If you have exactly one asymmetric carbon with inverted stereochemistry, then the diastereomer is a special one: an epimer. Anomers (e.g. α- and β-D-glucose) should be considered special cases of epimers.

Let me use the menthol isomers (image taken from Wikipedia, where a full list of authors is available) to clarify the concept:

Menthol isomers

Two vertically aligned structures are always enantiomers. Two structures that are not vertically aligned are diastereomers.

(+)-Isomenthol is (+)-menthol’s C4-epimer, while ($-$)-neoisomenthol is (+)-menthol’s C1-epimer. And ($-$)-neomenthol is (+)-menthol’s C2-epimer. All of these are also diastereomers.

(+)-Neomenthol is not an epimer of (+)-menthol. It is still a diastereomer, however.

  • $\begingroup$ Thank you so much for that great answer! I would love to accept this answer however sadly I can only accept one answer. $\endgroup$
    – Nanoputian
    Apr 22, 2016 at 2:23
  • 1
    $\begingroup$ @Nanoputian Well you can change the accepted answer ;þ Or apply a bounty. But I’m fine anyway ^^ $\endgroup$
    – Jan
    Apr 23, 2016 at 18:58
  • $\begingroup$ You can extend flow chart, by including nob-anomeric epimers in epimers. $\endgroup$ Dec 12, 2016 at 7:13
  • $\begingroup$ @AnubhavGoel Not all possibilities are listed. For example, there are diastereomers that are neither geometric isomers nor epimers. $\endgroup$
    – Jan
    Dec 12, 2016 at 15:46

epimers as compounds which differ by configuration at only one carbon

Yes, at only one centre.

However isn't that the same thing as diastereomers?

No, not completely. Diastereomers differ at least at one, but at less than all stereocentres. If two compounds would differ at all stereocentres, they would be enantiomers.


As far as epimerism in open form carbohydrates is concerned, examining the Fischer projections using a German mnemonic derived from the signal horn sounds of police cars (ta-tü-ta-ta) might help. Yes, sounds weird ;-)

Let ta and be $\ce{OH}$ on either side of the projection.

Then, glucose is ta-tü-ta-ta, whereas galactose is ta-tü-tü-ta. Apparently, they differ at one stereocentre. Consequently, they are epimers.

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    $\begingroup$ Thanks for clearing that up. What about 'carbohydrates in open form can have two different chirality centres and still be epimers' ? Is this statement correct? $\endgroup$
    – Nanoputian
    Apr 21, 2016 at 8:05

Yes you are correct that epimers are a subset of diastereomers.

Diastereomers are compounds that have similar configuration at some carbon and dissimilar configuration at some carbons.

Whereas epimers are compounds that differ in configuration at only one chiral carbon.

The point of difference arises in the fact that epimers have only one chiral carbon which is different in configuration whereas diastereomers can have any number of different configuration around its chiral carbons (except all being different).

  • $\begingroup$ They are chiral carbons, not achiral carbons (although IUPAC seems to prefer "chirality centre" now) $\endgroup$ Apr 21, 2016 at 11:18

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