I. SPECTROSCOPY 1. a) Give the number of expected signals (ignore splittings) in the ¹H and 13C NMR spectra of the following compounds: ¹H NMR: 13C NMR: 10 b) Sketch the ¹H NMR spectrum for the compound below. Be sure to consider chemical shifts, coupling patterns, and relative intensities between each spin system when drawing your spectrum. Label all non-symmetrically related H's on the structure (e.g. a,b,c, etc) and show what peak they correspond to on the spectrum: 9 8 7 H3C 6 CH3 (ppm) 5 Name 4 3 2 1 0

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I. SPECTROSCOPY
1. a)
Give the number of expected signals (ignore splittings) in the ¹H and 13C NMR
spectra of the following compounds:
¹H NMR:
13C NMR:
10
b)
Sketch the ¹H NMR spectrum for the compound below. Be sure to consider
chemical shifts, coupling patterns, and relative intensities between each spin system when
drawing your spectrum. Label all non-symmetrically related H's on the structure (e.g. a,b,c,
etc) and show what peak they correspond to on the spectrum:
9
8
7
H3C
mor
CH3
6
(ppm)
5
Name
4
3
2
0
Transcribed Image Text:I. SPECTROSCOPY 1. a) Give the number of expected signals (ignore splittings) in the ¹H and 13C NMR spectra of the following compounds: ¹H NMR: 13C NMR: 10 b) Sketch the ¹H NMR spectrum for the compound below. Be sure to consider chemical shifts, coupling patterns, and relative intensities between each spin system when drawing your spectrum. Label all non-symmetrically related H's on the structure (e.g. a,b,c, etc) and show what peak they correspond to on the spectrum: 9 8 7 H3C mor CH3 6 (ppm) 5 Name 4 3 2 0
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