Answer 2)
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2. Match the electron impact (El) mass spectrum with the correct structure from the choices below....
2. Match the electron impact (El) mass spectrum with the correct structure from the choices below. ectra of the following molecules (write the correct letter in the upper left-hand corner of the spectra). Draw the structure of the indicated fragments (*) A OH *(43) *(71) * (43) 100- MS-NU-O1 Relative Intensity Relative Intensity 10 20 30 40 50 70 80 90 100 10 30 40 60 70 50 /z 60 /z m m
Predict the molecular ion peak pattern (EI spectrum - low resolution) for the following species (show the line pattern with relative abundances, masses, and [M]+/[M+2]+, etc. designations). 60 10 m/z 3. Predict the molecular ion peak pattern (El spectrum - low resolution) for the following species (show the line pattern with relative abundances, masses, and [M]*[M+2]*, etc. designations). ii. CIBr iv. CaH&SO4 ii. CaH Br2 CSH11CI i.
11. The mass spectrum below is that of benzyl 3-methylbutanoate (see structure below). Provide a structure for the fragments at m/z 144, 129, 116, 115, 101, 99, 73, 71 and 43 (You must show the fragmentation pattern) (0.5x84 pts) 100 43 80 71 115 60 99 40 101 88 144 116 20 125 100 75 50 25 m/z 11. The mass spectrum below is that of benzyl 3-methylbutanoate (see structure below). Provide a structure for the fragments at m/z 144,...
Use the data below from an electron impact mass spectrum of a pure compound to deduce its structure. Draw your structure. PART 1: m/z relative intensity 52 31 50 100 15 2 PART 2: m/z Relative intensity 17 1.6 16 100 15 89 14 20 13 11
mass spectrometry matching to graphs 1. (2 points) Match the following mass spectra below to the correct structure below. One structure per spectra. All four compounds will not be used. A) CH:CH-CH(CH3)2 B) CH:CHOHCH.CH C) CH.CH:OCHCH D) CH:CH NHCH.CH Relative Intensity 10 20 30 40 50 60 80 90 100 110 120 70 /z m Relative intensity
Use the data below from an electron impact mass spectrum of a pure compound to deduce its structure. Draw your structure in the drawing window. Data selected from the NIST WebBook https://webbook.nist.gov/chemistry Relative intensity 1.0 25 m/z 73 72 57 43 29 100 17 You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. In cases where there is more than one answer, just draw one.
Use the data below from an electron impact mass spectrum of a pure compound to deduce its structure. Draw your structure in the drawing window. Data selected from the NIST WebBook, https://webbook.nist.gov/chemistry/ m/z Relative intensity 96 94 94 100 15 47
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
is is the mass spectrum of 2-pentanol. 100 MS-NW-8471 6 80 60 40 20 omt 10 20 30 40 60 70 80 50 m/z Provide a reasonable fragmentation pathway for the indicated fragments. Make sure that you discuss the relative intensity of the same fragments. | m/z 27.0 7.6 29.0 5.3 31.0 5.0 41.0 5.8 43.0 13.7 44.0 7.5 45.0 100.0 55.0 18.7 73.0 7.1