For the compound adamantine,how many different signals would you see in the ¹³C NMR? (Assume that you can see them all.)

Question

Quizplus · Accepted Answer

Adamantine has four non-equivalent carbon atoms, which would give rise to four different signals in the carbon NMR spectrum. However, the given NMR notation (¹³C) indicates that only two carbon atoms are being observed. Therefore, only two different signals would be seen in the spectrum, corresponding to the two observed carbon atoms.

For the Compound Adamantine,how Many Different Signals Would You See