
Interpretation:
In Figure 16-34, a line to represent the path of an ion that is too light to reach the detector is to be drawn and labeled as “too light.” The same is to be done for an ion that is too massive to reach the detector and to be labeled as “too massive.”
Concept introduction:
Mass spectrometry provides insight into the mass of a molecule and the fragments that compose it. Unlike spectroscopy, however, mass spectrometry does not involve
Once vaporized, these gaseous molecules, M (g), drift through a beam of fast moving electrons. When an electron from that beam impacts a molecule of M (g), an electron from M (g) is knocked off, producing a gaseous species that has one fewer electron and therefore has a positive charge. The process of producing this molecular ion, M+ (g), is called electron impact ionization and can be represented by Equation 16-6.
A charged species like M+ (g) can be guided into a detector through a curved tube using a magnetic field to bend the ion’s path. The extent that a given ion’s path is bent depends on the strength of the magnetic field that is applied and the mass-to-charge ratio of the particle, represented as m/z. If the magnetic field strength is held fixed, then only ions of a specific value of m/z can reach the detector. Ions with m/z different from that value will collide with the wall of the tube and will be destroyed before reaching the detector; those that are too light will be deflected too much whereas those that are too massive will not be deflected enough. If multiple ions with different m/z values are present, then the magnetic field strength can be adjusted to allow the various ions to be detected. The detector itself is designed to keep track of the number of charged species that collide with it; this number is translated into what is called the relative abundance of the ion. The greater the number of charged species detected, the greater the ion’s relative abundance. If multiple ions are produced with different values of m/z, then the magnetic field strength can be scanned to determine the relative abundance at each m/z.

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Chapter 16 Solutions
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
- How to draw this mechanism for the foloowing reaction in the foto. thank youarrow_forwardPredict the major products of the following organic reaction: Some important notes: CN A? • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. No reaction. Explanation Check Click and drag to start drawing a structure. 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Centerarrow_forwardDraw the major product of the following reaction. Do not draw inorganic byproducts. H3PO4 OHarrow_forward
- Predict the major products of this organic reaction: HBr (1 equiv) Δ ? Some important notes: • Draw the major product, or products, of this reaction in the drawing area below. • You can draw the products in any arrangement you like. • Pay careful attention to the reaction conditions, and only include the major products. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. • Note that there is only 1 equivalent of HBr reactant, so you need not consider the case of multiple additions. Explanation Check X ©2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacyarrow_forwardFor the structure below, draw the resonance structure that is indicated by the curved arrow(s). Be sure to include formal charges. :ÖH Modify the second structure given to draw the new resonance structure. Include lone pairs and charges in your structure. Use the + and - tools to add/remove charges to an atom, and use the single bond tool to add/remove double bonds.arrow_forwardUsing the table of Reactants and Products provided in the Hints section, provide the major product (with the correct stereochemistry when applicable) for questions below by selecting the letter that corresponds to the exact chemical structures for the possible product. OH conc Hydrochloric acid 40°C Temp A/arrow_forward
- Using arrows to designate the flow of electrons, complete the reaction below and provide a detailed mechanism for the formation of the product OH conc Hydrochloric acid 40°C Temp All chemical structures should be hand drawn on a piece of paper Paragraph BI UAE +varrow_forwarddraw out the following structures plesearrow_forwardDraw everything on a piece of paper outlining the synthesis from acetaldehyde to 2 cyclopentene carboxaldehyde using carbon based reagants with 3 carbons or fewers. Here is the attached image.arrow_forward
- Manoharan Mariappan, FR.D., 34) Complete the following reaction starting from hex-1-yne proceeding via different substitution reactions forming 2-heptanone. (25 pts). A Sia₂BH H₂O₂ NaOH Br D Mechanism for reaction D - ether-cleavage: 10 B Ph-MgCI, THF H₁₂O+ D HBr (XS) C TsCl, Py CH3-CH2-CH2-ONaarrow_forwardIn the table below, the correct structure for (2R)-3-methylpentan-2-ol (IUPAC name) can be represented by the letter OH OH HE > ' ÕH C B OH D A/ E OHarrow_forwardPredict the major products of the following organic reaction: + A Δ ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Check Click and drag to start drawing a structure. Save For Later 2025 McGraw Hill LLC. All Rights Reserved. Terms of Usearrow_forward
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