can you help me finish
analzying the MS peaks

can you help me finish analzying the MS peaks Bare Reak- Relative Intensity a elevage 25...
can someone help me wirh this IR?
1=(1-48) Solid as strand melty 98 completed wity NOVEMBER MS 100 - Relative Intensity wil T 0- 50 100 TITIT 75 m/z 125 150
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
This is the mass spectrum of dichlorocyclohexylmethylsilane. Explain the relative intensity for peaks at m/e 196.0 (13.5), 197.0 (1.8), 198.0 (9.1),199.0 (1.1), 200.0 (1.7)and 201.0 (0.2) 1 00 - MS-IW-7601 C1 80 $i-CH3 60 40 mtt O 40 zO 60 140 160 180 200 100 1ZO m/z Relative Intensity
This is the mass spectrum of dichlorocyclohexylmethylsilane. Explain the relative intensity for peaks at m/e 196.0 (13.5), 197.0 (1.8), 198.0 (9.1),199.0 (1.1), 200.0 (1.7)and 201.0 (0.2) 1 00 - MS-IW-7601 C1...
i
need to know the mass spect major peaks / interpretation and the
relavent chunks for both compounds. first compound is 9-fluorenone
& the second is benzaldehyde.
Corbonylketone Stretch Relative Intensity bag peak M + o p ptrerthyreprottoportthroporti tromptlebrujifuerontharepotepo 25 50 75 100 125 m/z pe 175 KUM! 150 matcher mass for 9- fluorenone MS VOUR M & base peak Relative Intensity 0 - 10 Hitler 30 40 50 60 20 80 90 100 120 70 m/z 110 106 base...
The MS spectra shows the following unknown. It is
either Toluene (C6H5CH3), Benzyl Bromide (C6H5CH2Br), m-cresol
(C6H4(OH)CH3), or Ethanol (C2H5OH)
Show work and label the appropriate peak and discuss the peaks in
text.
*Please explain how to do this*
100 MS-NW-2671 80 40 20- O 75 100 125 150 175 m/z 50 25 60 Relative Intensity
what are possible structures for each spectra
100 MS 80 - 60 Relative Intensity 40 20- 0 10 20 30 40 60 70 80 50 m/z 100- 80 Relative Intensity 40 20 0 10 15 20 25 30 35 40 50 55 60 65 70 75 80 45 m/z
Use the IR and MS data to elucidate the structures of the compounds below. Identify the M and other necessary peaks in the mass spectra below. Give the functional group responsible for the IR signals. IR: (1 709) sharp, strong (1607-1653) weak MS: ID 4 peaks 100- Relative Intensity orta pripreme 10 20 30 40 50 60 70 80 90 100 m/z 110 120 IR: (1753) strong (1602 - 1658) weak MS: ID 4 peaks 100 MS-NU-18 Relative Intensity 10...
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)...
Using the provided MS and IR spectra, predict the structure
and identity of the unknown. Show all workings and reasoning.
Identify important peaks or fragments that led to your conclusion.
You are free to use Rule 13 and/or index of hydrogen deficiency
when necessary.
2 /3 65% 2. Unknown B 100 MS-Nu-0323 80 60 40 20- 0 ptoinittm 25 50 75 100 125 m/z to three different elemental oxygen present. Note that there be may up L00 1000 st0 aVENUERId...
Please label the peaks of the following graphs for the compound
Acetophenone
100 Relative Intensity 100 110 120 Ortofritt 10 20 30 40 50 60 70 80 90 m/z f. NMR Spectrum: 11 10 9 8 5 4 2 1 ppm g. IR Spectrum: THESE TERCEIP HAVENUMERI