HNMR splitting for this molecule. . .

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rippinitez

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I'm trying to figure out why this molecule shows two singlets and not 1 singlet and 1 doublet. Because of symmetry, the methyl H's would show up as 1 singlet and the H's on the ring would show up as one doublet right?


View attachment nmr.png
 
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the methyl H would be a singlet (with an integration of 6), and those on the ring would be 1 singlet with integration of 4?

(identical H cAnnot "see" (split) each other)

just like for ethane, you will not get 1 multiplet, but 1 singlet.
 
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