1. 2.
I am trying to learn how to interpret 1H-NMR for the two above spectrums. How would you interpret these 1H-NMR spectrums to determine the shape of the molecule whose formula is C13H9NO3?
Formula of the compound is C13H9NO3.
Double bond equivalence = C + 1 - H/2 + N/2 = 13 +1 - 9/2 + 1/2 = 10
Stucture of the compound is:
Analysis of 1H NMR:
2Ha ; doublet; 8.35 ppm
2Hb; doublet; 7.95 ppm
2 Hc; doublet; 7.8 ppm
1He; triplet; 7.65 ppm
2 Hd; triplet; 7.50 ppm
How would you interpret these 1H-NMR spectrums to determine the shape of the molecule whose formula is C13H9NO3
Can you please explain, in detail, how to draw a 1H NMR and 13C NMR spectrum from a bond-line structure. Molecular formula is C7H10BrClS, please convert to bond-line structure for corresponding spectrums.
for
the 1H NMR spectra, draw the molecule with the given formula that
would have each soectra.
C8H.4. This is an alkyne. The relative integrations of the signals are I = 3, II = 9, III = 2. 8 5 4 PP 3 2 0 CgH:02. The singlet at 8 = 3.9 has an integration of 3, and the signals in the 8 = 1-8 region in total have an integration of 5. C8H802. The singlet at 8 = 3.9...
A compound with a molecular formula of
C7H14O has a 1H NMR spectrum as
follows. Based on the proton NMR and the molecular formula, you can
determine that the molecule is what?
A compound with a molecular formula of C7H140 has a H NMR spectrum as follows. Based on the proton NMR and the molecular formula, you can determine that the molecule is what? 6H 4H PPM None of these applies Contains methane (CH4) Has a plane of symmetry Chiral...
How would I interpret this 1H-NMR of
trans-9-(2-phenylethenyl)anthracene
(C22H16)?
integration values from left to right are 1.00, 0.66, 3.13, .31,
.25
1Η ΤΗ 14 13 12 11 10 -1 Chemical Shift (ppm)
How many signals would the following molecule show in its 1H NMR spectrum? b) 1 c) 6 cd) 8
9. Use the NMR data and chemical formula to determine the structure of the molecule. a) Formula: C5H100 TH NMR 13C NMR triplet quartet 200 180 160 140 30 60 40 20 0 120 100 Am b) Formula: C3H100 TH NMR 13C NMR singlet singlet doublet doublet 2 2 3 3 8 2 00 180 160 140 120 100 30 60
How many 1H-NMR signals would
you expect for each of the two starting materials in the reaction
shown below? Please draw the reaction product for the reaction
shown below. What are the approximate chemical shifts for each of
the hydrogen atoms in the molecule?
16. Propose a structure for a molecule of formula CaHsCl which gave the following 1H NMR spectrum. PPM 17. Propose a structure for a molecule whose mass spectrum shows a parent ion at m/z 148, an IR peak at 1680 cm'and gives the following H and 13C NMR spectra 3H зн 2H 2H 2H 3 5 2 7 6 4 PPM 160 140 180 60 220 200 20 0 120 100 80 40 PPM -
Help interpret this NMR graph
The molecular formula is C5H12O
the molecular weight is 88
Unknown 016 6H Copyright 1994 1H 4H 1H 3. 2. 1. 1.0 PPH Proton NMR 10 PPM0 Carbon 13 NHR
Please answer the question above.
The 1H NMR spectrum below corresponds to a molecule with the formula C4H5O. Its IR spectrum has important bands at 945, 1015, 1665, 3095, and 3360 cm^-1 Deduce and draw the structure of the unknown compound.