
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Annotate the Mass Spec, 1H NMR, and 13C NMR for C4H11N or Butylamine
Annotate the Mass Spec, 1H NMR, and 13C NMR for C4H8O or Butraldehyde
Annotate the Mass Spec, 1H NMR, and 13C NMR for C5H8O or Cyclopentanone
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Transcribed Image Text:Relative Intensity
100-
60
40
20-
0-
10
20
30
Mass Spec
40
t
50
m/z
(as of molecular font
60
70
80
73)
90

Transcribed Image Text:11
10
9
8
7
6
¹H NMR
5
ppm
4
2
0
200
180
COS-03-467
160
140
120
13C NMR
100
ppm
80
60
40
20
0
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- Draw the splitting pattern and assign and label the H of the spectrum of C4H8Oarrow_forwardThe mass spectrum of Compound C is shown below: Draw the most likely species responsible for the signals at m/z 91.arrow_forward7) Chemical Formula: C₂H₁N IR: weak peak at 3400cm-1 7 1H SH 2H 8) Chemical Formula: C8H1204 IR: strong peak 1720cm-1, peak at 1650cm-1 Unknowns for 1H NMR Final Report 9) Chemical Formula: C5H1002 IR: strong peak at 1750cm-1 1H (8~27 = 16-+2 = € /2=2. PPM 4H 2H 3 PPM 3H 3H 2 * H - (8x2) = 16-12=412=2 -G-H H h+1= 2 4 6H 6Harrow_forward
- Determine the compound (name or structure) from the data. Explain features from each data. Molecular formula: C6H5Br Use molecular formula to determine IHD IR: Identify the presence/absence of five key functional groups NMR: Analyze this last. Consider multiplicity and peak area to confirm compound. The 5 H peak area covers both peaks (at 7.1 and 7.5 ppm Structure?arrow_forwardGiven the following molecule, draw its predicted standard spectrum along with DEPT 90 and DEPT 135 spectra. Then, based on that picture, assign the numbered carbons on the original structure to a peak in the standard 13C spectrum. Provide a brief explanation for your choices.arrow_forwardWhich functional group, except alkane, is presence in the following IR spectrum? INFRARED SPECTRUM Relative Transmittance 0.96 0.92 carboxylic acid ether alcohol alkene 3000 2000 Wavenumber (cm-1) m 1000arrow_forward
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