Part 2. Complete the table predicting only the number of signals (number of types of carbon) for 13C NMR. For 1H NMR, predict the number of signals (number of types of hydrogen). For each of these signals, predict the splitting multiplicities (from the number of neighbors), and the total number of hydrogen atoms that belongs to that signal. (Please see the first row as an example) Number of 1H signals expected Number of 13H signals expected Compound Multiplicity 6H (triplet), 4H (sextet) H2 2 „CH3 H2 Br CH3 C CI

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NMR spectroscopy problems

Part 2. Complete the table predicting only the number of signals (number of types of
carbon) for 13C NMR. For 1H NMR, predict the number of signals (number of types of
hydrogen). For each of these signals, predict the splitting multiplicities (from the number of
neighbors), and the total number of hydrogen atoms that belongs to that signal. (Please see
the first row as an example)
Number of 1H
signals expected
Number of 13H
signals expected
Compound
Multiplicity
6H (triplet), 4H
(sextet)
H2
2
„CH3
H2
Br
CH3
C
CI
Transcribed Image Text:Part 2. Complete the table predicting only the number of signals (number of types of carbon) for 13C NMR. For 1H NMR, predict the number of signals (number of types of hydrogen). For each of these signals, predict the splitting multiplicities (from the number of neighbors), and the total number of hydrogen atoms that belongs to that signal. (Please see the first row as an example) Number of 1H signals expected Number of 13H signals expected Compound Multiplicity 6H (triplet), 4H (sextet) H2 2 „CH3 H2 Br CH3 C CI
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