can someone help me wirh this IR?Homework Answers
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can someone help me wirh this IR?
1=(1-48) Solid as strand melty 98 completed wity NOVEMBER...
3. Below are the MS and IR spectra of Compound A. a. Determine its structure. b....
3. Below are the MS and IR spectra of Compound A. a. Determine its structure. b. Identify pertinent peaks on the IR. Relative Intensity 25 50 75 125 150 175 100 m/z
Unknown 315-S20-2 Can someone help me fill out the table on the right side please IR...
Unknown 315-S20-2
Can someone help me fill out the table on the right side
please
IR Spectrum:
Unknown # 315-S20-2 Mol. Wt. = 181.0 g/mol C-33.17% H=5.01% 0 = 17.68% Molecular Formula Degree of Unsaturation = Mass Spectrum IR spectrum (liquid film) 100- Relative Intensity 150 175 25 50 75 100 125 m/z Based on the M.W., circle & label the molecular ion peak (M). Spectrum Region Frequency (cm ) Peak Shape (sharp, broad) MAVUTO Peak Intensity (strong, med., weak)...
can you help me finish analzying the MS peaks Bare Reak- Relative Intensity a elevage 25...
can you help me finish
analzying the MS peaks
Bare Reak- Relative Intensity a elevage 25 50 100 125 150 m/z
Please help propose interpretations of the spectra for the two unknowns pictured below. Identification and drawing...
Please help propose interpretations of the spectra for the two
unknowns pictured below. Identification and drawing of the unknowns
would be much appreciated and will get a thumbs up.
Liquid T alcohol MS Relative Intensity 0- r 10 20 30 40 50 70 80 90 100 60 m/z Liquid T "H-NMR broad singlet, IH doublet, 6H quartet, 2H triplet, 2H nonet, IH PPM C-NMR PPM Sold e Carboxylic acid Mass Spec. 100 Relative Intensity optippropri protiletterturmflopperprompt 25 50 75 100...
could someone help asap please Degrees of Unsaturation: S Label Considerations, Comments Absorbance Max Relative Intensity...
could someone help asap please
Degrees of Unsaturation: S Label Considerations, Comments Absorbance Max Relative Intensity Shape Functional group by bridization Considerations, Comments Shin Signal Label Integration Multiplicity Adjacent protons Hydrogen type mass 1 #1 Final Answer: Unknown 295 (30.29% C,254% H) 4000 3200 2300 2400 2000 180 1600 1400 1400 1200 10) 800 Fi 100- 80 Relative Intensity 40 201 0-trirnitrpm 25 Tim SO 75 125 150 100 m/z
5. Given the spectral data below, provide a structure. Note you must assign all of the...
5. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR or MS that assisted you in deriving your answer. (6 pts.) 6H, d 3H, d 2H, d 1H, sextet 1Hm Relative Intensity M+ = 164 50 75 125 150 100 m/z 2000 Wavnumber icm-1)
please help... ignore the written work 1) Which compound gives the following spectra? For the 'H-NMR...
please help... ignore the written work
1) Which compound gives the following spectra? For the 'H-NMR assign all signals. Interpret mol peak and base peak in the mass spectrum if a mole peak exists. Assign at least two "c signals. How does the IR spectrum support your findings? (12 pts.) s, 4 H s, 3 H t, 3 H q, 2h s, 1 H 2 1 6 5 4 7 8 11 10 ppm esce 100- 80 40 20 150...
Please help propose interpretations of the spectra for the unknown picture below. Identification and drawing of...
Please help propose interpretations of the spectra for the unknown
picture below. Identification and drawing of the unknowns would be
much appreciated and will get a thumbs up.
samdo carboylic acid Mass Spec. Relative Intensity p o-tryptofii prototipropilepto 50 75 100 m/z 125 150 Solid B H-NMR multiplet, SH singlet, 11 broad singlet, 1H broad singlet, 1H PPM "C-NMR 180 160 140 120 100 PPM 8b6b 4620
Can someone please help me interpret the IR data of a diels alder reaction product between...
Can someone please help me interpret the IR data of a diels
alder reaction product between 9-anthracenemethanol and
N-methylmaleimide. Can you show the DA product structure with the
various H species associated? Thank you.
90 Joe lan Diels Alder product 85 80 75 70 65 60 55 50 45 40 35 30 25 3000 2500 500 3500 2000 1500 1000 4000 Wavenumbers (cm-1) % Transmittance 6 3069.03 1766.39 1681.46 1474.36 1465.21 1455.61 1382 93 1295.54 1282.09 1318.30 1209.16 1141 30...
Determine the structure of Compound 2 using the Mass Spec, IR, C NMR, H NMR, and...
Determine the structure of Compound 2 using the Mass Spec, IR, C
NMR, H NMR, and Dept Experiments.
Splitting patterns are as follows from left to right: triplet, 5
peaks (unsure of name), septet (7), 4 peaks (unsure of name),
doublet
Compound 2 Mass Spec MT:M/2 = 164 Relative Intensity 25 50 75 125 150 100 m/z IR LO0 D 4000 3000 2000 1500 1000 500 HAVENUMBERI-i H NMR: ditto as compound 1 6 2 2 4 1 2 PPM...
3. Below are the MS and IR spectra of Compound A. a. Determine its structure. b. Identify pertinent peaks on the IR. Relative Intensity 25 50 75 125 150 175 100 m/z
Unknown 315-S20-2
Can someone help me fill out the table on the right side
please
IR Spectrum:
Unknown # 315-S20-2 Mol. Wt. = 181.0 g/mol C-33.17% H=5.01% 0 = 17.68% Molecular Formula Degree of Unsaturation = Mass Spectrum IR spectrum (liquid film) 100- Relative Intensity 150 175 25 50 75 100 125 m/z Based on the M.W., circle & label the molecular ion peak (M). Spectrum Region Frequency (cm ) Peak Shape (sharp, broad) MAVUTO Peak Intensity (strong, med., weak)...
can you help me finish
analzying the MS peaks
Bare Reak- Relative Intensity a elevage 25 50 100 125 150 m/z
Please help propose interpretations of the spectra for the two
unknowns pictured below. Identification and drawing of the unknowns
would be much appreciated and will get a thumbs up.
Liquid T alcohol MS Relative Intensity 0- r 10 20 30 40 50 70 80 90 100 60 m/z Liquid T "H-NMR broad singlet, IH doublet, 6H quartet, 2H triplet, 2H nonet, IH PPM C-NMR PPM Sold e Carboxylic acid Mass Spec. 100 Relative Intensity optippropri protiletterturmflopperprompt 25 50 75 100...
could someone help asap please
Degrees of Unsaturation: S Label Considerations, Comments Absorbance Max Relative Intensity Shape Functional group by bridization Considerations, Comments Shin Signal Label Integration Multiplicity Adjacent protons Hydrogen type mass 1 #1 Final Answer: Unknown 295 (30.29% C,254% H) 4000 3200 2300 2400 2000 180 1600 1400 1400 1200 10) 800 Fi 100- 80 Relative Intensity 40 201 0-trirnitrpm 25 Tim SO 75 125 150 100 m/z
5. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR or MS that assisted you in deriving your answer. (6 pts.) 6H, d 3H, d 2H, d 1H, sextet 1Hm Relative Intensity M+ = 164 50 75 125 150 100 m/z 2000 Wavnumber icm-1)
please help... ignore the written work
1) Which compound gives the following spectra? For the 'H-NMR assign all signals. Interpret mol peak and base peak in the mass spectrum if a mole peak exists. Assign at least two "c signals. How does the IR spectrum support your findings? (12 pts.) s, 4 H s, 3 H t, 3 H q, 2h s, 1 H 2 1 6 5 4 7 8 11 10 ppm esce 100- 80 40 20 150...
Please help propose interpretations of the spectra for the unknown
picture below. Identification and drawing of the unknowns would be
much appreciated and will get a thumbs up.
samdo carboylic acid Mass Spec. Relative Intensity p o-tryptofii prototipropilepto 50 75 100 m/z 125 150 Solid B H-NMR multiplet, SH singlet, 11 broad singlet, 1H broad singlet, 1H PPM "C-NMR 180 160 140 120 100 PPM 8b6b 4620
Can someone please help me interpret the IR data of a diels
alder reaction product between 9-anthracenemethanol and
N-methylmaleimide. Can you show the DA product structure with the
various H species associated? Thank you.
90 Joe lan Diels Alder product 85 80 75 70 65 60 55 50 45 40 35 30 25 3000 2500 500 3500 2000 1500 1000 4000 Wavenumbers (cm-1) % Transmittance 6 3069.03 1766.39 1681.46 1474.36 1465.21 1455.61 1382 93 1295.54 1282.09 1318.30 1209.16 1141 30...
Determine the structure of Compound 2 using the Mass Spec, IR, C
NMR, H NMR, and Dept Experiments.
Splitting patterns are as follows from left to right: triplet, 5
peaks (unsure of name), septet (7), 4 peaks (unsure of name),
doublet
Compound 2 Mass Spec MT:M/2 = 164 Relative Intensity 25 50 75 125 150 100 m/z IR LO0 D 4000 3000 2000 1500 1000 500 HAVENUMBERI-i H NMR: ditto as compound 1 6 2 2 4 1 2 PPM...
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