IR spectrum
The IR spectrum contains sp3 CH stretching around ~ 2950 cm-1
C=O stretching is present ~ 1700 cm-1
Mass spectrum
The molar mass of the compound is 130 m/z
1H NMR
The quartet and triplet from 4.0 ppm and 1.3 ppm belongs to ethyl group which attached to oxygen directly. The The peak 2.2 ppm belongs to CH3 group which is attached to carbonyl carbon. The another peak at 3.3 ppm is belongs CH2 that lies between two carbonyl group. Using all the information we can deduce the structure.
Problem 5 C6H1003 Wave Number, om' 1500 1200 1100 1000 4000 2000 2000 2000 1500 10...
Compound 21 is a liquid (boiling point 60" C) that has Z stereochemistry. The Mass, IR, and H NMR spectra, along with 13C NMR data, are given below. Elemental Analysis: C, 24.78; H, 208; contains a halogen Mass Spectrum 61 96 98 30 40 50 60 70 80 90 100 110 120 130 140 150 180 170 180 190 200 mVe Infrared Spectrum Wave Number, cm - 4000 3000 2500 1500 2000 1300 1200 1100 800 700 1000 900 ww...
Compound is a liquid, boiling point 136 C. The Mass, IR, and H NMR spectra, along with C NMR data, are given below. Elemental Analysis: C, 90.51; H, 9.49. Mass Spectrum 106 30 50 70 500 110 120 130 140 150 100 170 ao 10 2001 mie Infrared Spectrum Wave Number, om 4000 3000 2500 2000 1500 1300 1200 100 1000 900 10 13 11 Wavelength, microns H NMR 2 pom, & Structure: C Spectral Data: singlet, 140.2 ppm doublet,...
4) Unknown 428 (29.30% C,5.74% H) 4000 3600 3200 2800 2400 2000 1800 1800 1400 1200 1000 300 600 100- Relative Intensity 10 20 30 40 50 60 80 90 100 110 120 70 m/z peo ppm 10 ppm Chemical Formula: Degrees of Unsaturation: Label Absorbance Max Relative Intensity Shape Functional group/hybridization Considerations, Comments Signal Label Shift Integration Multiplicity Adjacent protons Hydrogen type Considerations, Comments Molecular Ion mass Special Considerations, Comments (e.g. nitrogen, bromine, or chlorine present?) #4 Final Answer:
Use the following wave spectrum to identify the chemical
structure
Problem 11.10 60 40 Exact M.S. (CI) 129.1279 FT-IR (NEAT) 20 UVAmax BLANK 4000 3000 2000 800 WAVENUMBERS (CM) 1200 1000 100. Mass Spec. CI 70eV 60 55 40 43 129 20 40 60 70 80 100 110 120 40 m/s 13C NMR 62.3 MHz COCI CDCI luuluuluu 50 40 30 20 10 120 S00 70 130 160 150 140 170 H 500 MHz 3H CDCla 5.2 Hz/mm H 10H...
need help elucidating this please
IR Spectrum liquid 4000 3000 2000 2000 1600 V (cm) 1000 1200 1200 00 100F Mass Spectrum M . 152 280 80 120 180 200 240 40 m / expansion 13C NMR Spectrum (100 O MHE. COCI, solution 130 120 pm DEPT CH CH. CH 10178 por proton decoupled 08 (ppm) 40 80 120 200 160 'H NMR Spectrum (400 MH. COCI, solution) 70 74 pp 5 4 3 2 8 (ppm) 10 9
help me create a molecule
Frequency (cm1) 5000 4000 3000 2500 2000 1700 1500 1400 1300 1200 1100, 1000 900 00 T 800 700 8910 1 12 Wavelength () 13 15 Cl 呎
1600 1500 . 1400 1300 1200 1100 1000 900 800 30 35 40 45 50 55 60 Lean Body Mass Strongly curvi-linear O Roughly linear O Both answers are correct. Save and Subn
1. What is the chemical formula of the unknown?
2. what is the mass of the unknown?
3. What is the HDI?
4. According to IR spectra, what functional groups are
present?
5. What is the structure of the molecule?
138 PRACTICAL SPECTROSCOPY Compound 80 is a liquid (boiling point 212 C), that can be prepared by the reaction of Compound 79 with acidic, anhydrous ethanol. The Mass, IR, and 'H NMR spectra, along with C NMR data, are given...
please help explain the gc fragmentation for this?
132.0 3500 104.0 3000 MW-140.16 2500 2000 1500 78.0 1000 51.0 500 63.0 83.8 88.9 n/z--> 40 45 50 55 60 70 80 85 90 95 100 105 110 115 120 130 135 140 125 75 65
Question #1 (10 Marks) 500 1000 1500 2000 2500 3000 3500 200 650 1100 1550 2000 2450 2900 3350 100 100 100 100 100 100 100 1005001600 250 500 500 500 500 500 500 500 1400 50 200 1000 400 125 600 S0 8001O 1000 2000 1200 8SD 400 400 400 Complete the Total Planned Expenditure (AE) column for all levels of income (Y) on the above table. a) What is the consumption function? Complete the equation. C- 200 b)...