5. Using the letter designations, rank the following compounds from lowest carbonyl stretching frequency to highest. 100 lowest highest 6. For the following molecule, provide the number of peaks you expect in each ¹H NMR signal due to splitting in the boxes provided. 80 60 40 7. a. Circle the compound below that corresponds to the IR spectrum shown. & Olan gota arte OLOCH, -OCH₂ -CH₂ H 20 *-=Aze-zu OL 4000 لو سلو سلم (b) A 3500 3,5 3000 4 H₂C EL CH-O CH3 B H3C 2500 4.5 wavelength (um) 5 5.5 6 7 8 9 10 2000 1800 1600 1400 1200 1000 wavenumber(cm) 11 12 13 14 15 16 800 600

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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5. Using the letter designations, rank the following compounds from lowest carbonyl stretching
frequency to highest.
100
lowest
highest
6. For the following molecule, provide the number of peaks you expect in each ¹H NMR signal
due to splitting in the boxes provided.
80
60
40
7. a. Circle the compound below that corresponds to the IR spectrum shown.
& Olan gota arte
OLOCH,
-OCH₂
-CH₂
H
20
*-=Aze-zu
OL
4000
لو سلو سلم
(b)
A
3500
3,5
3000
4
H₂C
EL
CH-O
CH3
B
H3C
2500
4.5
wavelength (um)
5 5.5 6
7
8 9 10
2000 1800 1600 1400 1200 1000
wavenumber(cm)
11 12 13 14 15 16
800
600
Transcribed Image Text:5. Using the letter designations, rank the following compounds from lowest carbonyl stretching frequency to highest. 100 lowest highest 6. For the following molecule, provide the number of peaks you expect in each ¹H NMR signal due to splitting in the boxes provided. 80 60 40 7. a. Circle the compound below that corresponds to the IR spectrum shown. & Olan gota arte OLOCH, -OCH₂ -CH₂ H 20 *-=Aze-zu OL 4000 لو سلو سلم (b) A 3500 3,5 3000 4 H₂C EL CH-O CH3 B H3C 2500 4.5 wavelength (um) 5 5.5 6 7 8 9 10 2000 1800 1600 1400 1200 1000 wavenumber(cm) 11 12 13 14 15 16 800 600
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