# CH2 group in alkyl glucoside gives two separate HNMR signals

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It seems like the CH2 next to the sugar gives two different NMR signals which is very interesting. Could someone explain me why?

• The real question is why all the other $\ce{CH2}$ groups don’t ;)
– Jan
Nov 23 '17 at 14:51

Without the sugar, those two hydrogen atoms are enantiotopic, since substitution of those protons would lead to different enantiomers. Achiral measurements still will appear identical though.

Once the sugar is attached, the two hydrogens are diastereotopic, and are chemically and magnetically different. Especially so close to the chiral environment of the sugar, these two hydrogen see enough of a difference in their local environments that their shifts are different.

I would like to expand on Zhe's excellent explanation. The concept of why these hydrogens are in different environments is one that often befuddles people who are just learning about NMR spectroscopy. There is an example in the literature that I can no longer find in which the authors were unaware that the methylene hydrogens in diethyl α-methyl malonate were non-equivalent. [One of the co-authors won a Nobel Prize in Chemistry. So don't feel bad!] Imagine that you are chemistry's version of Maxwell's demon. You sit on the red hydrogen of ethyl bromide and look at the bonded carbon. What do you see? A clockwise (CW) environment in the Cahn-Ingold-Prelog (CIP) sense [Br>CH3>H]. When you sit on the blue hydrogen the environment is counterclockwise (CCW). Now you are more capable than an NMR spectrometer. You can distinguish between enantiotopic hydrogens. But the spectrometer can't tell the difference, the same result that was observed by the questioner. In a chiral environment, either by doctoring the sample with a chiral chelating species or by having a chiral environment proximate to the methylene group in question, a distinction can be made. Notice that the methylene group close to the glucose moiety displays diastereotopic hydrogens (circles) while the ones next to the phthalimide group (triangles) are not resolved in spite of the fact that they, and every methylene group in the chain, bear diastereotopic hydrogens!

Now consider (S)-1-bromo-2-methylbutane (CW-S). Sitting on the red hydrogen you see the same order of substituents Br>C>H (CW) as on ethyl bromide but the carbon has an S-configuration. Now jump over to the blue hydrogen of the S-bromide. The local environment is CCW but C2 is still of the S-configuration. That is to say, CW-S and CWW-S have diastereotopic hydrogens! We can use the same arguments with the R-enantiomer where CW-R and CWW-R have diastereotopic hydrogens. The racemate displays the same diastereotopic hydrogens as do the enantiomers. Finally, the 400MHz NMR spectrum of cholesterol [http://sdbs.db.aist.go.jp/sdbs/cgi-bin/direct_frame_top.cgi] displays the two methyl groups at the end of its chain as separate diastereotopic groups separated by a mere 2 Hz even though there are three methylene groups between them and the nearest center of asymmetry. Resolution at low field is not to be expected but yet the hydrogens inherently remain different.

• The way people do this is to replace the atom of interest with a special one that has higher priority than the other. For example, you'd replace one of the hydrogens with $\ce{H}*$. Checking both hydrogens in the OP's question gives two different enantiomers without the sugar and two different diastereostereomers with the sugar.
– Zhe
Nov 27 '17 at 0:22
• One way to look at it. Nov 27 '17 at 0:43
• The detailed explanation was meant for the novice and not those in the know. Nov 27 '17 at 0:46