Hi Why would butan-1-ol have a singlet on its HNMR spectrum?
I thought there would be 3 triplets, a multiplet (5 splits) and a multiplet (6 splits)?
Also, I don't get why it has 5 H environments and not 4. I was told that Hs on the same C are always part of the same environment, but this contradicts that rule. Is that because the O-H on the first carbon is part of a different H environment than the other 2 Hs on that same C? (If so, why?)
Also if asked to draw more than 1 repeating polymer unit (e.g.: 4 repeating units all linked in a row with double bonds), would you still have to have the brackets and 'n' subscript at the ends?
Thanks
You'll hear the general rule that when counting the number of neighbouring hydrogens to predict the splitting of a signal is that you can't "go through" an oxygen atom. The basic concept (not in VCE) behind splitting is that neighbouring hydrogens exert their own magnetic field onto the hydrogens in that environment. However, in this case, the highly electronegative oxygen atom has enough of a deshielding effect on the hydrogen which is bonded to it, that the effect of the neighbouring hydrogens is neglible. This is why the signal does not split.
When intepreting the number of unique hydrogen environments, the hydrogen in the alcohol is counted as its own environment (since it produces it own peak on the NMR spectrum). We don't consider it to be "connected" to the carbon, or in the same environment. So, yes, the hydrogen in the hydroxyl group is in its own environment.
Unless the question specifically said the polymer was only 4 units long, you would still have to draw the brackets and the 'n' subscript to show that those 4 units are repeating. Without them, your structure tells the reader that the polymer only has 4 units.
Hope this helps