Can someone help me with an 1 H spectrum of a molecule which contains a morpholine ring? I have two H patterns of methylene of morpholine, so one of them has resonance signal 3.6 ppm (CH2-O) and the other resonance signal 2.2 ppm (CH2-N)...
Why the signal resonance of methylene close to N are a broad band (it seems to be a triplet but its not clear)?
and why the other signal close to O is a clear triplet? Why this difference?
And the last question, Why is the reason of 4 protons of methylene has the same resonance signal...? and other 4 protons too?
Thanks !