Mass spectrometry is a technique that determines the molecular formula of organic compounds by ionizing molecule samples and measuring their mass-to-charge ratios. During mass spectrometry, a molecule is bombarded with high-energy electrons, which causes the molecule to eject an electron and form a positively-charged molecular ion. The mass spectrometer then analyzes the masses of these ionized molecules. A mass spectrum plots the relative abundance of each ion versus its mass-to-charge ratio, revealing the molecular weight and structural information about the original molecule.
Mass spectrometry is a technique that determines the molecular formula of organic compounds by ionizing molecule samples and measuring their mass-to-charge ratios. During mass spectrometry, a molecule is bombarded with high-energy electrons, which causes the molecule to eject an electron and form a positively-charged molecular ion. The mass spectrometer then analyzes the masses of these ionized molecules. A mass spectrum plots the relative abundance of each ion versus its mass-to-charge ratio, revealing the molecular weight and structural information about the original molecule.
Mass spectrometry is a technique that determines the molecular formula of organic compounds by ionizing molecule samples and measuring their mass-to-charge ratios. During mass spectrometry, a molecule is bombarded with high-energy electrons, which causes the molecule to eject an electron and form a positively-charged molecular ion. The mass spectrometer then analyzes the masses of these ionized molecules. A mass spectrum plots the relative abundance of each ion versus its mass-to-charge ratio, revealing the molecular weight and structural information about the original molecule.
Mass spectrometry is a technique that determines the molecular formula of organic compounds by ionizing molecule samples and measuring their mass-to-charge ratios. During mass spectrometry, a molecule is bombarded with high-energy electrons, which causes the molecule to eject an electron and form a positively-charged molecular ion. The mass spectrometer then analyzes the masses of these ionized molecules. A mass spectrum plots the relative abundance of each ion versus its mass-to-charge ratio, revealing the molecular weight and structural information about the original molecule.
Mass spectrometry is a technique used for measuring the molecular
weight and determining the molecular formula of an organic compound. In a mass spectrometer, a molecule is vaporized and ionized by bombardment with a beam of high-energy electrons (~ 1600 kcal, or 70 eV). It takes ~100 kcal of energy to cleave a typical bond. The electron beam ionizes the molecule by causing it to eject an electron forming positive ions (the parent or molecular ion) and products from broken bonds (fragment ions). 1 Mass Spectrometry Instrumentation 2 Mass Spectrometry When the electron beam ionizes the molecule, the species that is formed is called a radical cation, and symbolized as M + . The radical cation M + is called the molecular ion or parent ion. The mass of M + represents the molecular weight of M. Because M + is unstable, it decomposes to form fragments of radicals and cations that have a lower molecular weight than M + . The mass spectrometer analyzes the masses of cations. A mass spectrum is a plot of the amount of each cation (its relative abundance) versus its mass to charge ratio (m/z, where m is mass, and z is charge). z is almost always +1, m/z actually measures the mass (m) of the individual ions. 3 Mass Spectrometry Consider the mass spectrum of CH 4 below: The tallest peak in the mass spectrum is called the base peak. The base peak is also the M peak, although this may not always be the case. Though most C atoms have an atomic mass of 12, 1.1% have a mass of 13. Thus, 13 CH 4 is responsible for the peak at m/z = 17. This is called the M+1 peak. 4 Mass Spectrometry The mass spectrum of CH 4 consists of more peaks than just the M peak. Since the molecular ion is unstable, it fragments into other cations and radical cations containing one, two, three, or four fewer hydrogen atoms than methane itself. Thus, the peaks at m/z 15, 14, 13 and 12 are due to these lower molecular weight fragments. 5 Mass Spectrometry A mass spectrum: 6 Chapter 12 7 Fragmentation of the Hexane Radical Cation Chapter 12 8 Mass Spectrum of n-Hexane Groups of ions correspond to loss of one-, two-, three-, and four- carbon fragments. Chapter 12 9 Fragmentation of Branched Alkanes The most stable carbocation fragments form in greater amounts. Chapter 12 10 Mass Spectra of Alkanes 11 Mass Spectra of Alkenes Resonance-stabilized cations favored. Chapter 12 12 Mass Spectra of Alcohols dehydration dehydration + cleavage -cleavage leading to stabilized ions Cleavage leading to stabilized ions Mass Spectrometry Alkyl Halides and the M + 2 Peak Most elements have one major isotope, notable exceptions: Chlorine: 35 Cl and 37 Cl, which occur naturally in a 3:1 ratio. Thus, there are two peaks in a 3:1 ratio for the molecular ion of an alkyl chloride. The larger peak, the M peak, corresponds to the compound containing the 35 Cl. The smaller peak, the M+2 peak, corresponds to the compound containing 37 Cl. Br has two isotopes 79 Br and 81 Br, in a ratio of ~1:1. Thus, when the molecular ion consists of two peaks (M and M + 2) in a 1:1 ratio, a Br atom is present. Iodine may be lost as I + (127) a gap of 127 in the spectrum as well as a peak at m/z = 127. 15 Mass Spectrometry Alkyl chlorides and the M+2 peak 16 - Cl (difference of 35) Mass Spectrometry Alkyl bromides and the M+2 peak 17 - Br (difference of 79) Mass Spectrometry High Resolution Mass Spectrometers Low resolution mass spectrometers report m/z values to the nearest whole number. Thus, the mass of a given molecular ion can correspond to many different masses. High resolution mass spectrometers measure m/z ratios to four (or more) decimal places. This is valuable because except for 12 C whose mass is defined as 12.0000, the masses of all other nuclei are very closebut not exactlywhole numbers. The Table lists the exact mass values for a few common nuclei. Using these values it is possible to determine the single molecular formula that gives rise to a molecular ion. 18 Mass Spectrometry High-Resolution Mass Spectrometers Consider a compound having a molecular ion at m/z = 60 using a low-resolution mass spectrometer. The molecule could have any one of the following molecular formulas. 19 Mass Spectrometry Gas Chromatography-Mass Spectrometry (GC-MS) 20 Used to detect drug and drug metabolites from bodily fluids e.g. sport drug testing Mass Spectrometry Gas Chromatography-Mass Spectrometry (GC-MS) To analyze a urine sample for tetrahydrocannabinol, (THC) the principle psychoactive component of marijuana, the organic compounds are extracted from urine, purified, concentrated and injected into the GC-MS. THC appears as a GC peak, and gives a molecular ion at 314, its molecular weight. 21 Mass Spectrometry Other useful information Compounds of carbon/hydrogen/oxygen have even mass number parent ions and odd mass number fragments, for example: Compounds of that contain nitrogen, such as amines, have odd mass number parent ions and even mass number fragments, for example: Also an example of -cleavage