Three isomeric compounds with nearly identical boiling points were produced by a CH337 student and injected on the OSU-Cascades Shimadzu gas chromatograph instrument as described in the lecture notes. The resulting chromatogram is shown below. I compound has nearly identical boiling points, determine the relative polarity of each peak by filling in the blanks with the Roman numerals I, II, or III only. Compound is most polar. Compound is least polar. Intensity 3000- I II 2000- III 1000- 0-

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Three isomeric compounds with nearly identical boiling points were produced by a CH337 student and injected on the OSU-Cascades Shimadzu gas chromatograph instrument as described in the lecture notes. The resulting chromatogram is shown below. If each
compound has nearly identical boiling points, determine the relative polarity of each peak by filling in the blanks with the Roman numerals I, II, or III only.
Compound
is most polar.
Compound
is least polar.
Intensity
3000-
I
II
2000-
III
1000-
2.0
2.1
2.2
2.3
2.4
2.5
2.6
2.7
2.8
2.9
3.0
min
Transcribed Image Text:Three isomeric compounds with nearly identical boiling points were produced by a CH337 student and injected on the OSU-Cascades Shimadzu gas chromatograph instrument as described in the lecture notes. The resulting chromatogram is shown below. If each compound has nearly identical boiling points, determine the relative polarity of each peak by filling in the blanks with the Roman numerals I, II, or III only. Compound is most polar. Compound is least polar. Intensity 3000- I II 2000- III 1000- 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 2.8 2.9 3.0 min
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