You are going to start with benzene, and proceed through molecule A on your way to molecule B. Use the NMR/IR spectra to solve for molecule A and B. Next show the synthetic route to get to molecule B.
Molecule A:C13H18O
Molecule B:C14H22O
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You are going to start with benzene, and proceed through molecule A on your way to...
2. Starting with benzene, proceed through molecule E on your way
to molecule F. Use the NMR/IR spectra to solve for molecule E and
F. Show the synthetic route to get to molecule F.
Molecule E:C12H16O
Molecule F: C14H22O
100 롷 50 4000 3000 2000 1500 1000 500 HAVENUMBERI-1 ЗН 4H 2H ЗН 1Н 2H 1Н 10 нар 0 PPM مد =[ [ 400 3000 [0 1500 100 500 أ- HAVEHLIHE EFI ЗН ЗН 2H ЗН 4H ІН 2H 1Н...
You are going to start with benzene, and proceed through
molecule A on your way to molecule B. Use the NMR/IR spectra to
solve for molecule A and B. Next show the synthetic route to get to
molecule B.
Molecule A:C13H180 100 50 way D 4 DOO 5000 2000 1500 1000 sbo NAVENUHBERI- ЗН ЗН ЗН 4H 2H IH 2H HA 8 7 6 5 2 0 PPM Molecule B:C14H220
For pyridine.....
(a) Show each potential intermediate that can be generated when
an electrophile adds to pyridine. Use a generic E for the
electrophile.
(b) Draw all the resonance structures for each potential
intermediate
(c) State whether the most stable intermediate occurs for ortho,
meta or para substitution. Provide an argument (15 words or
less).
(d) You are going to start with benzene, and proceed through
molecule A on your way to molecule B. Use the NMR/IR spectra to
solve...
of the four compounds listed below which would produce the
spectra below?
Which molecule is consistent with both of these IR and TH NMR spectra? 100 6H 50 3H 1H 4000 3000 1000 500 2000 1500 WAVENUMBERS Na PPM onthlon OB. Ос. OD OH
What is the major product of this reaction? MeNH2 H30+ HN HN a A B C D A B C D Which molecule is consistent with both of these IR and 'H NMR spectra? 100 6H mo 50 ЗН 1H 0 4000 3000 1000 500 2000 1500 WAVENUMBERS 3 PPM oogle он oli oh oth он D. HO
Use the IR and NMR spectra to confirm the identity of
your final product. Identify all of the important peaks in the IR
spectrum. Assign all peaks in the NMR spectrum to their respective
hydrogen nuclei.
IR and 1H NMR of 9-Fluorenone: LOD TFRITTEN 9000 2000 LOOD MAVENUISERI 2 3 PPM 5 4H 8 2H2H 9 IR and 1H NMR of 9-Fluorenol: 100 TRANSMETTANCEI D 4000 3000 2000 1500 1000 500 HAVENUBIRII 1H 2H2H 2H 2H TH 9 5 3...
Please identify my unknown molecule and label all spectroscopy
data with key information leading to your conclusion.
Unknown H411 DD 500 1000 2000 3000 4000 NAVENUMBERI-1 Unknown H411 q 0 20 100 80 120 160 140 180 200 ppm COS-07-311 Unknown H411 100 MS-NW-5797 80 - 60 40 M* 0 175 150 125 100 50 75 25 m/z Relative Intensity 20 Unknown H411 ЗН, d ЗН, t ЗН, m 2H, dq 2H, m 1H, m 2 4 PPM 6 7...
Propose a reasonable structure for this compound based on the mass spec, IR, and NMR data. 100 Relative Intensity M+ 10 20 30 40 60 70 80 90 50 m/z LUU TRINETTRICET 4000 3000 2000 cm1 1500 1000 500 ЗН Зн 2H тттттттттттттттттт 11 10 9 8 7 6 5 4 ppm 200 180 160 140 120 80 60 40 20 100 ppm
s and give the m 0~시 2. How could you distinguish the following pairs of isomeric compounds using IR and MS? For some pairs- one of these spectral techniques may be different enough to distinguish the compounds. and (b) and 3. Analyne the IR and MS spectra below to predict a possible structure for each compound. Label the major peaks or (a) C,110 1500 1000 (b) CsHro 3000 2000 1500 1000 m/z ollowing problem is to ys ar wwight of...
Can you help to figure out the formula and the structure
?
50) 4. Determine the structure of the molecule from these spectra, and draw your answer in the box. 100 80 40 20 4000 2000- 3000 1500 1000 400 100 -[ 196 80 196 40 20 200 20 40 60 80 100 120 140 160 180 200 3H,t 2H,m 2H,t 2H,m 3 2 peaks 20 80 100 120 140 160 180 200 3H,t 2H,d 2H,d 2H,m 2H,t 2H,m 8...