For the following problems, Identify major peaks with M-X (peaks > 40 relative intensities), M, and where appropriate M+1, M+2 peaks. Identify the major peaks in the FTIR sample. Use all of this information to determine the structure of the compound. 5) C5H11N 100 - S--3224 80 - 60 - 40 - 20 - 10 20 30 40 50 60 70 80 m/z Draw the structure below: Relative Intensity

Q: 10 3H 3H 2H

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Q: Normal Carbon 177.24 62.9 37.4 34.1 25.2 22.5 19.0 DEPT-135 no peak + + + + DEPT-90 no peak no peak…

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Q: 100 80 60 40 20 % of base peak 40 45 59 V (cm¹) M+ = 60 (<1%) 120 80 160 m/e 800 Mass Spectrum 1200…

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Q: An unknown compound B has the following spectra. Write the masses for the M+ , аnd (M+1)+ peaks.…

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Q: MİCRONS 5.5 2.5 100 26 27 28 2,9 3 3.5 4,5 11 12 13 90 70 50 40 30 20 1773 cm 10 3800 300 3400 3200…

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Q: Identify the important peaks in the following MS spectral data and draw the structure of the…

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Q: %Transmittance 105 100 95- 90 85 80 75 70 65 60- 55- 50 45- 40 35- 30- 25 20 15- 10 50 3600 0000…

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Q: Tw_wmm IR Spectrum (liquid film) 4000 00 80 60 -40 20 % of base peak 3376 40 10 3000 59 13C NMR…

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Q: C11H11BrO2 No peaks exchange with D20

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Q: Which of the following compounds matches the given data? MS: base peak = 71 Mt= 105 ; M+2 = 107…

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Q: Normal Carbon 209.7 84.3 57.6 40.5 34.3 27.7 23.1 DEPT-135 no peak + + DEPT-90 type of carbon no…

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Q: 4958 METHYL-M-NITROBENZOATE-CARBON 200 180 160 140 120 100 80 60 40 20 ppm 86 9T 8- - 52.7

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Q: OSE COOT cone DOST → HAVENUMBERI-F 2000 3000 OOEF *** 個個 TRANSMITTANCE 001

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