why not?

Started by prsndwg
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prsndwg

Full Member
10+ Year Member
Hi,
Can someone explain why the answer is not choice C and its Choice A instead??

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What about this one?

23wjimh.jpg


I thought it was two singlets and 2 doublets.. but i guess not😕


I think The answer should be E-two singlets. since this compound has symmetry, all the carbons in the ring will be considered as one while being next to the carbon which has no hydrogens on it-the one with the methyl, which would give a singlet. Also, the methyl itself would be the other singlet since it is adjacent to the same carbon mentioned above.
I hope thats correct
 
I think The answer should be E-two singlets. since this compound has symmetry, all the carbons in the ring will be considered as one while being next to the carbon which has no hydrogens on it-the one with the methyl, which would give a singlet. Also, the methyl itself would be the other singlet since it is adjacent to the same carbon mentioned above.
I hope thats correct

Now i get it..
another Q.. If this was 13C NMR how many would that be? would it be 4 singlets?