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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.
The NMR spectrum of protons:
* [katex]^{\rm{1}}{\rm{H NMR}}[/katex] Spectroscopy.
The number of hydrogen atoms attached at a carbon position determines the number of peaks in proton NMR spectrumcopy.
[katex]\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}[/katex]
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, while three hydrogen Atoms display 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.
Answer