2-PENTANONE
1) In the NMR spectrum, we note that there are 4 distinct peaks, so we know that in the molecule, there are four different types of hydrogens.
2) The area of the individual peaks gives the sum of 10, in line with the empirical formula C 5 H 10 O, so the area declared at the top of the peaks corresponds to the number of hydrogen atoms that produce that signal.
3) The molecule C 5 H 10 O contains a double bond, in fact if it were saturated with hydrogens would contain 12 (2n + 2). Because it contains a carbonyl, the double bond is here, the rest of the molecule is saturated.
4) The two signals at d 2.45 and d 2.09 corresponding to the hydrogens on the carbon next to the carbonyl which absorb in the range between d 2 and d 3. The other two peaks at d 0.96 and d 1.61 corresponding to hydrogen instead of carbon primary and secondary respectively.
7) Analyzing the molecule of 2-pentanone we can confirm the assignment of the peaks for both the chemical shift, both for the multiplicity (indicated in the figure in parentheses.)
2-pentanone
IR
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MASS
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13 CNMR
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RAMAN
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MASS
13 CNMR
RAMAN
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