Molecular formula mass is 122
The ratio of M:M+2 peak is 1:1
So the halogen atom is Bromine.
From 1H -NMR 6 Hydrogens doublet indicate the presence of isopropyl group
(CH3)2-CH-
1 Hydrogen atom multiplet at 3.9 ppm indicates the presence of following group.
(CH3)2-CH-Br
Hence the structure of the compound is
(CH3)2-CH-Br
IR spectral data:
Peak at ~2900 cm-1 indicates the presence of alkane C-H ( sp3 C-H)
Peak near ~800 cm-1 indicates the presence of C-Br bond
1H -NMR:
(CH3)2-CH-Br
a b
Protons a: 6 H doublet at 1.2 ppm
Protons b: 1 H multiplet at 3.9 ppm
13 C -NMR:
Carbon a: peak at 28
Carbon b : peat at 45
1. label all spectra in IR 2. figure out structure. label a,b,c,d, etc in structure and...
1. label all spectra in IR
2. figure out structure. label a,b,c,d, etc in structure and
corresponding letter on all peaks in HMNR and CNMR
3. show all calculations
IR/HNMR/CNMR MW=122: 124 AMU 1:1 11 10 200 150 160 140 120 100 ppm 100 0
1. label all spectra in IR
2. figure out structure. label a,b,c,d, etc in structure and
corresponding letter on all peaks in HMNR and CNMR
3. show all calculations
IR/HNMR/CNMRT MW=88 AMU 9.3 T. 2 T. 2 Broads, Рprm 200 150 160 140 120 100 pom 80 O 40 20
Determine structure of unknown compound by deducing the formula
and analyzing the spectra.
Part C:S IR/HNMR/CNMR Unknown #93 MW=134 AMU / ring SOC-H dromul 5,311 - Overlapping Signals, 4 1,34 HEP-11-24 ppm 4 Signals 120-160 ppm 200 180 20-0-075 160 240 120 80 40 20 100 pon
For the following unknown, annotate the corresponding spetras
and determine the molecular formula and lewis structure.
Anknown IR/HNMR/CNMR MW=122 : 124 AMU 1:1 D 3000 1000 00 RYENUEERI D, 6 M, 1 10 7 4 1 HP-03-172 Ppm N 10 120 60 100 80 40 20 200 180 160 140 ppm CDS-00-26O
For the following unknown, annotate the corresponding spetras
and determine the molecular formula and lewis structure.
Unknown # s IR/HNMR/CNMR 1 MW= 88 AMU AVENUE S, 3 T, 1, 2] Broads, Ppm 200 160 140 180 120 80 40 60 20 ó 100 rpm
I need help figuring out what the molecular formula and
structure look like based on the molecular weight 142 AMU and also
based in the info given in the IR, HNMR, and CNMR.
IR/HNMR/CNMR Unknown #101 MW=142 AMU Czol D2 | M 1 ppm 200 150 160 140 120 100 ao so 10 20 rpm
6. The CNMR and HNMR spectra of acetylferrocene are shown below. Paste the spectra into your notebook. Assign the peaks in each spectrum. (Draw the product molecule and label the atoms A, B, etc) a. 200 180 1 140 120 100 80640 20 0 . 11 107653 2
IR/HNMR/CNMR Unknown #102 MW-110 AMU 0 -H C=0 Wavenumber(em-1) Broads.s.2 3 overlapping signals, 4 FM EN ppm 20 0 200 180 160 12010030604020 rpm
Label the significant peaks in the IR and NMR spectra. When analyzing the signals in the 'HNMR, be sure to include all appropriate information. For example: 3H, singlet, 0 neighbors, and c (the letter referring to the corresponding unique type of hydrogens that were labeled in the structure). It is recommended to provide more analysis for each signal than what is described above, when necessary, such as labeling any coupling constants if any are provided For NMR label each peak...
IR spectroscopy 1. Match the following six compounds to the IR spectra shown below. Draw the structure in the box. On the spectra, mark all important peaks with arrows or circles, and label them with corresponding bonds. NH2 orte de Structure: IR Spectrum lould film) 1723 V 4000 2000 3000 1200 1600 V (cm ) Structure: IR Spectrum fiquld fam) 4000 2000 V (cm 16001200800 ) Exp - 119- Exp. 100 Structure: 3600-2500 IR Spectrum liguld fm) U 1715 4000...