-COOH 811-812 O x - - .o. -C For each compound: 1. Determine the number of...
For each compound: 1. Determine the number of equivalent hydrogens - number of different signals 2. Determine the splitting pattern of each signal 3. Sketch a possible spectrum 4. Then try to match the compound to the correct NMR spectrum er w t & You We were unable to transcribe this imageWe were unable to transcribe this imageWe were unable to transcribe this imageNMR worksheet H-1 (proton NMR D for each compound 1. Debamia the number of equivalent hydropens number...
NMR worksheet: H-1 (proton) NMR -COOH کد 11 وه اسط .)= X For each compound: 4. Then try to match the compound to the correct NMR spectrum ! بر ♡ na = = = | ۲۲ OMIT this peak added in error) small broad peak (OH) $ PPM We were unable to transcribe this image
NMR worksheet: C-13 NMR somatic cuct c-a.c-- - --- LLLLLLLLLLLLLLLLLLLLLLL Ester C=O approx. 170-180 ppm For each compound: 1. Determine the number of equivalent carbons 2. Predict and sketch the location of the peaks 3. Then try to match the compound to the correct NMR spectrum 3. & Lond. 6. B O DO do 1howo 10 120109
"Determine the structure of each compound. For each NMR below, draw the determined structure and annotate( correlate the equivalent protons with the corresponding NMR signals in the spectrum)." All work must be very neat and organized. you need to organize your thoughts, please use o separate sheet of paper. Below are six IH NMR spectra from six different compounds. The molar mass for each compound is given. Determine the structure of each compound. For each 'H NMR spectra below, draw...
10/24/2019 A compound with molecular formula C.H.., has the following NMR Spectrum. Determine the number of protons giving rise to the peak at 2.0 ppen. Give the splitting patter expected for the indicated 'H-NMR signal bi double c) triplet Id quartet (el quintet 5.0 45 40 3.5 3.0 2.5 Integration Values 20 15 10 0.5 ppm 19.4 37.9 6.33 v e or what is the ofte Recolher the integrowa monitor there ? Predict the multiplicity of the signal indicated below...
Predicting the Spectrum MR and C NMR) the expected 'H NMR number of si spectrum for the following molecule. Be sure to include appropriate for the following molecule. Be sure to er of signals, show spisina ar try to indicate relative Integration by arca un (label peak with some splitting and try to indicate relative Integration by area under peak peak with correct number for clarity in tabel all the unique hydrogens with letters and assign them to the peaks...
NMR worksheet: C-13 NMR - || - | |-- alkanes Ester C=0 approx. 170 - 180 ppm For each compound: 1. Determine the number of equivalent carbons 2. Predict and sketch the location of the peaks 3. Then try to match the compound to the correct NMR spectrum بز به م . . We were unable to transcribe this image
PROBLEM 16.20 Determine the number of signals that would be generated in the 'H NMR spectrum of each of the following compounds, and predict the splitting pattern of each signal. CI CI CICI (a) (c)
Please explain all steps. Include degrees of unsaturation, functional groups, and signals used to determine structure. For the compounds listed below: 1. (18 points) Label each set of chemically equivalent protons, using a for the set that will be have the lowest frequency (most upfield) in the 1H NMR spectrum, b for the next a. lowest, and so on. of each set of the equivalent protons. expected for each compound. b. Indicate the splitting pattern (singlet, doublet, triplet...) for expected...
Determine the structure of each compound for each 1H NMR spectrum. Draw the determined structure and annotate (correlate the equivalent protons with the corresponding NMR signal(s) in the spectrum). Compound E, M = 164.20 g/mol io 8 PPM Compound F, M = 108.14 g/mol PPM