
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
Organic Chemistry: Principles And Mechanisms (second Edition)
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- Predict the products of this organic reaction: CH3-C-O-CH2-CH2-C-CH3 + H₂O ? A Specifically, in the drawing area below draw the condensed structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. No reaction Click anywhere to draw the first atom of your structure. :☐ darrow_forwardDE d. Draw an arrow pushing mechanism for the following IN O CI N fo 人 P Polle DELL prt sc home end ins F5 F6 F7 F8 F9 F10 F11 F12arrow_forwardPredict the products of this organic reaction: + H₂O H* ? A Specifically, in the drawing area below draw the skeletal ("line") structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. No Reaction Click and drag to start drawing a structure.arrow_forward
- Predict the major organic products of the reaction below and draw them on right side of the arrow. If there will be no significant reaction, check the box below the drawing area instead. C Cl CH, OH There will be no significant reaction. + pyridine G Click and drag to start drawing a structure.arrow_forwardWhat is the missing reactant in this organic reaction? H R+ H2O Δ OH 0= CH3-CH-O-CH3 + CH3-C-OH Specifically, in the drawing area below draw the condensed structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer box under the drawing area. No Answer Click anywhere to draw the first atom of your structure. dyarrow_forwardYou are trying to determine whether the following organic reaction can be done in a single synthesis step. If so, add any missing reagents or conditions in the drawing area below. If it isn't possible to do this reaction in a single synthesis step, check the box below the drawing area instead. Note for advanced students: if you have a choice of reagents to add, you should choose the least reactive and most economical reagents possible. Cl It isn't possible to do this reaction in a single synthesis step. + T OHarrow_forward
- Predict the products of this organic reaction: CH3 O CH3-CH-C-O-CH2-CH2-CH3 + H₂OH+ Η ? A Specifically, in the drawing area below draw the condensed structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. No Reaction Click anywhere to draw the first atom of your structure.arrow_forward€ CH3-CH-C-O-CH2-CH2-CH3 + NaOH A? Specifically, in the drawing area below draw the condensed structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. Predict the products of this organic reaction: CH3 O Click anywhere to draw the first atom of your structure. No reaction ✓ Garrow_forwardA molecule can have a temporary or permanent depending on the structure and the way the electrons can move. True Falsearrow_forward
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