N,N-dimethylethylamine will give rise to the spectrum.
These peaks arise due to following fragmentation pattern,
CH3 has a molecular weight of 12+3=15 so, when a methyl fragment gets released the m/z value decreases by 15.
When CH3CH2 fragment gets released the m/z value decreases by 15+14=19. (Molecular weight of CH3 fragment is 15 and CH2 fragment is 14.)
m Relative Intensity - Which compound gives rise to the MS below? HN 58 100 N.N-dimethylethylamine...
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
100- Relative Intensity T 10 15 20 25 30 35 50 55 60 65 70 75 40 45 m/z
1. Assign structures for the following molecules given the IR and EI-MS data below: (a) IR shows medium intensity peak at 1650 cm and C-H out-of-plane bending at 880 cm. 56 Relative Abundance M(84) uli 35 40 45 dll 25 30 LL 15 20 . Inlll 50 55 miz 60 65 70 75 80 85 90 (b) IR has a broad peak at 3370 cm and a strong peak at 1159 cm!. The M ion is absent. Relative Abundance (percent)...
assign the base peak, molecular ion peak (with m/z) and identify
the structure?
please? :,)
MS-NU-5499 Relative Intensity 10 15 20 25 30 50 55 60 65 70 75 35 1 40 45 m/z
The spectra for the final product of hydroboration-oxidation of propyne are shown below: 100- M + Relative Intensity 10 15 20 25 30 35 50 55 60 65 70 75 40 45 m/z LOD TF RASMITTANEIZ! 4000 3000 2000 cm-1 1500 1000 500 2 H ppm 200 180 160 140 120 80 60 40 20 0 100 ppm Draw the structure of the final product of hydroboration-oxidation of propyne in the box provided. 1) BH3-THF 2) H2O2, NaOH H2O -...
CH3 Cl 100 Base 10) The El-MS of 2-chloro-2- methylpropane is shown at right. Draw the structure of the cation corresponding to the base peak. Clearly indicate where the charge resides. You need only show one of the two resonance forms. MS-NW-1505 no parent ion detected 92- Relative Intensity 10 15 20 25 30 35 40 55 60 65 70 75 80 45 50 m/z The 3:1 ratio of peak intensities at 77 and 79 m/z in the El-MS above...
Description: Shown below is an EI-MS spectrum for t-butyl chloride. 1) Clearly label the base peak in the spectrum. Draw the structure of the fragment the base peak corresponds to. 2) Is there a molecular ion present in the spectrum? If so, label the peak that corresponds to the molecular ion. 3) Is there any evidence that the following EI-MS spectrum represents a chlorine containing compound? If so, label the necessary peaks and explain briefly why there is sufficient evidence...
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
Identify the unknown and tell what compound is located at each
peak
# t 0-H nidhyde O AVENUE 100 - -0933 Relative Intensity 10 15 20 25 30 35 50 55 60 65 70 75 40 45 m/z 11 10 9 8 7 5 4 3 2 1 0 6 ppm HSP-00-002
Please explain the answer in details.
2. [5 marks] Use the mass spectrum (EI-MS) and the additional 'H NMR data to deduce the structure of the compound of the formula CgH603. 100 - 149 м (150) Relative Abundance (percent) 0+ரார்ராராராரா T ITIIIIIIIIIIIIIIIIINITITTITTTTTTTTTTTTTTTTTTTTTin 15 20 25 30 35 40 45 50 55 60 65 70 75 80 85 90 95 100 105 110 115 120 125 130 135 140 145 150 155 mz doublet singlet doublet