2. Draw the structure of the cation responsible for the base peak (m/z=58) in the mass spectrum of 3-aminopentane shown below:
3. Below is given the mass spectrum of a simple alkane. What is the chemical formula of the alkane? What is the name of the alkane? Explain how you determined the exact structure of the alkane from the observed fragments.
4. Below is a mass spectrum of an ester. Identify the ester. Consider that the dominant fragmentation pathway involves a-fragmentation at the carbonyl. Also the alkyl group attached to the ester oxygen is observed as a fragment in this spectrum (the m/z=70 peak is not very useful here).
2. Draw the structure of the cation responsible for the base peak (m/z=58) in the mass...
18. The mass spectrum of 2-methylpentan-3-ol is shown below. Draw the structure of the fragment ions of m/z= 73 and 59. Relative abundance (%) TTT 10 20 80 80 100 120 mi
5. Draw a structure for and name a compound that is consistent with compound that is consistent with the following MS. abundance 73 M 80 90 100 110 120 130 140 150 160 10 20 30 40 50 60 70 m/z Question 5: Structure and name: Mass Spectrum (include the molecular ion) Observed Fragment & MW Expected MW Fragmentation type Explanation:
Show what fragment is responsible for the base peak at m/z 44 in the mass spectrum of butan-2-amine
5 The parent peak in the mass spectrum shown below is at 100 80 6o 40 C 20 10 20 3 40 070 90 m/z (a) m/z 58 (b) m/z -71 (c) m/z - 86 (d) m/z 43 6 In mass spectrometry of the following organic compound, which of the following fragmentation pathway is not likely to occur? H3C CH H3C (a) dehydration (b) Alpha-cleavage (c) McLafferty rearrangement (d) All of these
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,...
The m/z of the M+ peak of an unknown is 146, and this peak is the base peak (i.e., the tallest peak). (See below mass spectrum of the unknown.) Combustion analysis data indicate 49.03% carbon and 2.74% hydrogen. The IR spectrum and 13C-NMR spectrum of this compound also were obtained and are shown below. Given this information, what is the name of this unknown molecule? MASS SPECTRUM 100 80 60 面 40 20 0.0 120 160 40 80 0.0 m/z...
Isovaleraldehyde (shown above), analyzed in the previous spectrum, fragments to form a cation with a m/z=71. Which is the structure of the cation responsible for this fragment from the options (A-D) below. ОА овес оо
The mass spectrum of pentanal shows a peak at m/z 43. The molecular weight of pentanal is 86. Draw the electron flow and products for the formation of the cation, m/z 43 and radical fragment. ? + ? M: 86 m/z 43 cation (M-43) radical
I am not understanding this assignment at all. Any assistance is very much appreciated. Mass Spectrum: Molecular Ion m/z value and structure of the Molecular Ion. Base Peak m/z value and structure of that ion One other significant peak m/z value and structure of that ion C13 NMR Spectrum-- Draw Structure of Compound on the C13 NMR spectrum and identify each signal with the appropriate Carbon. Proton NMR Spectrum-- Draw Structure of Compound on the Proton NMR spectrum and identify...
4 CIven the mass spectrum below, choose the structure which best matches the spectrum. For each peak (besides the molecular ion), draw the fragment which accounts for the peak. Rel. Abundance Mass 41 63 45 100 82 12 85 37 100 3 OH Which one matches the MS better? (circle) or Fragments: 41 45 82 85