**Title: Mass Spectrometry Fragmentation Analysis****Instructions:**For the following molecules, draw the structure for the fragment that you would expect to be the base peak. Upload your answers.**Molecular Structures Provided:**a. ![Molecule a](carbonyl_compound.png) - Structure: An organic molecule containing a carbonyl group (C=O) attached to an ethyl chain on one side and a propyl group on the other.b. ![Molecule b](benzene_compound.png) - Structure: An organic molecule with a benzene ring (six carbon atoms in a hexagonal ring) attached to a two-carbon alkyl chain.c. ![Molecule c](ether_compound.png) - Structure: An organic molecule containing an ether group (R-O-R') with an ethyl group on one side and a butyl group on the other.d. ![Molecule d](amine_compound.png) - Structure: An organic molecule with an amine group (NH₂) attached to an ethyl chain.**Explanation of Structure Identification:**In mass spectrometry, the base peak is the most intense peak in the spectrum and usually corresponds to the most stable fragment ion formed during the ionization process. When analyzing the provided molecules, consider the stability of carbocations, the fragmentation pattern typical to each functional group, and resonance stabilization.**Provide your answers:**Upload your sketches of the most stable fragment ions expected for each molecule to be the base peak.

The highest intensity peak in mass spectra is known as base peak. Base peak is the result of the…

Answered: For the following molecules, draw the…

For the following molecules, draw the structure for the fragment that you would expect to be the base peak. Upload your answers. a. P love b. d. NH₂

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Which one of the following statements is not true? O In mass spectrometry, the initially formed radical cation can sometimes survive and appear as a peak on the mass spe O Visible light is higher in energy than infrared light. O In mass spectrometry the peak corresponding to an ethyl cation fragment would appear at m/z 30. O In mass spectrometry, a benzylic cation would appear at m/z 91. O In IR spectroscopy, a C-O bond stretch would appear at a lower cm1 than a C=O bond stretch. %23 $ & 8 2 3 4 6 8 Q E R T. Y 4 5 2 K D G H. C || N M. alt
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Question 6 Question 6-1: Aromatic ethers can lose a neutral alkene molecule during fragmentation in a mass spectrometer as shown in Figure 6. What is the structure of the alkene formed by phenyl ethyl ether? [Give a SMILES notation.] Your answer Figure 6 H Your answer 0 Question 6-2: The loss of the alkene generates a fragment that registers the base * peak in the mass spectrum. What is the m/z value of the base peak?
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