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We recently did a lab/demo using the NMR to observe Na ions in sodium complexes in our Inorganic Class. I understand most of the post lab questions, but there are a few that still have me stumped. Essentially what we did was create two samples: in one we added NaI to 18-crown-6 ether (with enough deuterated acetone to lock the signal) and in the other we just added NaI to deuterated acetone. 1M NaCl was used as a standard. The resulting peak of the Crown solutiion was shifted downfield approximately -17 ppm from the NaCl standard. The peak from the Na in pure acetone was only about -1.7 ppm down from the standard. My questions are as follows:
1) How would you make the Na-23 NMR peaks "sharper" for NaI/18-crown-6 ether samples?
2)Why did we acquire all spectra without rotationg the sample?
3) Why are Na-23 peaks shifted to lower ppm values when sodium is encapsulated by 18-crown-6 ether
4) How would our results change if a cryptand, such as [2,2,2]crypt was used instead of 18-crown-6 ether.
Show all the steps in the mechanism for the following reaction, When benzene is mixed with deuterated sulfuric acid, deuterium is slowly incorporated onto the ring. Show the mechanism for this reaction and explain how this relates the sulfonation of ..
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