a. Molecular ion peak is at m/z = 112 since it corresponds to highest m/z value.
b. Base peak is the peak with highest intensity, so base peak is at m/z = 112
c. The peak at M+ and (M+2) correspond to peak at 112 and 114 respectively which indicates the presence of isotope of chlorine i.e. Cl 37 along with Cl 35. The ratio of these Cl37 to Cl 35 is 3:1.
d. The X in formula C6H5X is Cl. This can be identified based on presence of M and M+2 molecular ion peaks and their relative abundance in the ratio 3:1 which is possible for only Chlorine atom.
e. The m/z at 77 corresponds to C6H5+ i.e. benzene ring with one less proton.
1. Consider the Mass Spectrum below to answer the following questions: MS-NU-S495 Relative Intensity 0- 10...
Mass Spec Diethyl Phthalate Mass Spectrum Relative Intensity m/z MS diethylphthalate (note: major m/z values of 222, 193, 177, 149 are present) 3) Propose structures for TWO fragments in the mass spectrum. Note: the molecular ion peak at 222 m/z is NOT a fragment.
Use the mass spectrum to answer the questions below Does the compound contain chlorine or bromine or neither? Explain. Give the m/z value for the molecular ion peak. Give the m/z value for the base peak. The base peak is a common fragment – what is the most likely chemical formula for the base peak? Does the compound contain chlorine or bromine or neither? Explain. Give the m/z value for the molecular ion peak. Give the m/z value for the...
110 2. (1 points) The mass spectrum of 2-methyl-3-pentanol is shown below. Identify the fragments. 100- MS-NU-5456 Relative Intensity 0- t THAT it 20 TH 40 E 60 TITTTTTTTT 100 50 70 m/z
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...
15. The mass spectrum of a compound appears below. The molecular ion, M+1, and M+2 peaks have intensities of 100, 6.8, and 31.8 respectively. Use the information provided to determine the formula of the compound 100 MS-NW-5495 80 60 40 20 шшшl 110 10 20 30 40 50 60 70 80 90 100 m/z Relative Intensity 15. The mass spectrum of a compound appears below. The molecular ion, M+1, and M+2 peaks have intensities of 100, 6.8, and 31.8 respectively....
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
MS ID a minimum of two fragments excluding M Relative Intensity M : mle Nitrogen: Yes/No Halogen(s): 50 100 IR Label the peaks that characterize the structure Functional Group(s): HNMR Label each peak with the type of hydrogen from the structure Molecular Structure: What is the structure of the molecule for Integrated Spectra Problem #1?. Deduce it by using the molecular mass (M+) and fragment information on the MS spectrum, the IR functional groups, and the information from the H-...
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...
Intensity MASS SPECTRAL DATA Unknown m/e Relative Intensity Mass Spectrum (мм) 90 18.4 0.83 92 0.09 29 90 I5 60 m/e 2. Based on the mass spectrum, do you think your compound has a nitrogen atom? Explain. Propose at least two molecular formulas based on the mass spectrum and calculate the exact mass of the parent ion. Is one of your formula more likely than the other? If so, explain. 3.
Lab 6 Mass Spectrometry Worksheet Please show your work for the following problems in your laboratory notebook. Your notebook carbons will be collected at the beginning of the next lab period. 1. For each of the following molecular formulas, calculate the index of hydrogen deficiency (IHD), and draw at least two possible structures: a. CaH4 22+2--6+04-2 b. CaHs c. CoHsNO2 26)-54t 4 d. CHioBr2 2 215)+2--0+o 2. Write the molecular formulas for three hydrocarbons with the following molecular ion (M)...