Construct a simulated 1H NMR spectrum, including proton integrations, for CH3OC(CH2OCH3)3 (see Hint). Drag the appropriate…
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Question “Construct a simulated 1H NMR spectrum, including proton integrations, for CH3OC(CH2OCH3)3 (see Hint). Drag the appropriate…”
Construct a simulated 1H NMR spectrum, including proton
integrations, for CH3OC(CH2OCH3)3 (see Hint). Drag the appropriate
splitting patterns to the approximate chemical shift positions;
place the integration values in the small bins above the associated
chemical shift. Splitting patterns and integrations may be used
more than once, or not at all, as needed. Likewise, some bins might
remain blank. Note that peak heights are arbitrary and do not
indicate proton integrations.
Answer
The NMR spectrum of protons:
* Protone NMR spectroscopy can be used to predict the structure of a compound.
* In ^{\rm{1}}{\rm{H NMR}}
* There are also other spectroscopies such as ^{{\rm{13}}}{\rm{C NMR}}
* ^{\rm{1}}{\rm{H NMR}}
The number of hydrogen atoms attached at a carbon position determines the number of peaks in proton NMR spectrumcopy.
\begin{array}{l}\\{\rm{number of line = 2nI + 1}}\\\\{\rm{I = 1/2 for proton}}\\\\{\rm{n = number of hydrogen atoms at adjecent carbon atom}}\\\end{array}Below is the drawn structure.
The above structure contains three types of protons. Nine hydrogen atoms exhibit identical behavior (methyl atoms), six hydrogen Atoms display identical behavior (methyl groups), and three hydrogen Atoms exhibit identical behavior (methyl group next to oxygen).
Because none of the types has adjacent protons, three singlet peaks can be observed in proton NMR spectrumtra.
Below is a diagram of the proton NMR spectrum.
Ans:
Conclusion
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