A. 0.78 g | ||
B. 1.6 g | ||
C. 0.46 g | ||
D. 0.56 g | ||
E. Not enough information is given. |
A. 0.088 M | ||
B. 0.044 M | ||
C. 2.5 M | ||
D. 0.025 M | ||
E. 0.18 M |
A. 0.0237 m | ||
B. 0.592 m | ||
C. 0.118 m | ||
D. 4.26 m | ||
E. 0.00426 m |
A. 0.0043 ppb | ||
B. 0.043 ppb | ||
C. 430 ppb | ||
D. 4300 ppb | ||
E. None of the above |
A. 10.0 mL | ||
B. 4.00 mL | ||
C. 40.00 mL | ||
D. 2.50 mL | ||
E. 25.0 mL |
A. The results are accurate but not precise. | ||
B. The results are precise but not accurate | ||
C. The results are neither accurate nor precise. | ||
D. The results are both accurate and precise. | ||
E. The results are not enough information is given to determine accuracy or precision. |
A. 14% | ||
B. 5.1% | ||
C. 12% | ||
D. 98% | ||
E. 37% |
A. 1.6 µM | ||
B. 16 µM | ||
C. 1.6 mM | ||
D. 0.16 mM | ||
E. None of the above |
A. 1.37 M | ||
B. 6.50 mM | ||
C. 9.90 mM | ||
D. 8.06 mM | ||
E. 8.83 mM |
A. The volume of the standard added must be added with the volume of the sample used to give a new sample volume. | ||
B. The volume of the standard added is subtracted from the total volume of the sample used. | ||
C. The volume of the standard added can be ignored, because it is so small. | ||
D. The volume of the standard added can be ignored, because volumes are not used in the calculations. | ||
E. The volume of the standard added can be ignored, because it is part of the blank correction. |
A. The sensitivity of an analytical method is the same as its detection limit. | ||
B. The sensitivity of an analytical method is a measure of ability to determine whether slight differences in experimental results are significant. | ||
C. The sensitivity of an analytical method is the smallest amount of analyte that the instrument is able to measure. | ||
D. The sensitivity of an analytical method is the response of the instrument to human error. | ||
E. None of the above |
A. The detection limit of an instrument is the same as its sensitivity. | ||
B. The detection limit of an instrument is a measure of ability to determine whether slight differences in experimental results are significant. | ||
C. The detection limit of an instrument is the smallest amount of analyte that the instrument is able to measure. | ||
D. The detection limit of an instrument is the ability of the instrument to respond to an error. | ||
E. None of the above |
A. Electrochemical analysis methods | ||
B. Gravimetric analysis methods | ||
C. Tritrimetric analysis methods | ||
D. Spectroscopic analysis methods | ||
E. Photochemical analysis methods |
A. Conservation of energy | ||
B. Conservation of mass | ||
C. Constant compostition | ||
D. Definite proportions | ||
E. The law of gravity |
A. Carefully controlling the solution conditions | ||
B. Reprecipitation of the solid | ||
C. Digestion of the precipitate | ||
D. Thoroughly washing and drying the filtrate | ||
E. All of the above |
A. The amount of silver in a solution of silver nitrate | ||
B. The acidity of a water sample | ||
C. The amount of water in eposom salts | ||
D. All of the above | ||
E. None of the above |
A. The equivalence point of an acid-base titration is the same as the indicator endpoint. | ||
B. The equivalence point of an acid-base titration is the point where there is an equivalent amount of titrant and titrand. | ||
C. The equivalence point of an acid-base titration is where the pH = 7.0 (neutral). | ||
D. The equivalence point of an acid-base titration is where the entire volume of the buret has been used. | ||
E. The equivalence point of an acid-base titration is the average value of the dissociation constants. |
A. It is 1:6, because EDTA is a hexaprotic weak acid with six distinct acid dissociation values. | ||
B. It is 1:4, because EDTA has four binding sites upon loss of the four carboxylic acid protons. | ||
C. It is 1:2, because EDTA has two binding sites upon loss of the two ammonium protons. | ||
D. It is 1:1, because EDTA forms a cage-like structure around the metal ion. | ||
E. It is dependent on the metal ion present. |
A 58.3 mg sample containing Sn2+ is dissolved in 1.0 M HCl. If 23.6 mL of 0.010 M Tl3+ was required to titrate to endpoint, what is the mass percent (w/w%) of tin in the original sample?
A. 48% | ||
B. 28% | ||
C. 24% | ||
D. 40% | ||
E. 14% |
A. 18% | ||
B. 36% | ||
C. 1.6% | ||
D. 53% | ||
E. 47% |
A. c - concentration | ||
B. ε - molar absorptivity coefficient | ||
C. A - absorbance | ||
D. b - path length of the sample | ||
E. λ - wavelength |
A. The absorbance will double. | ||
B. The absorbance will quadruple. | ||
C. The absorbance will be halved. | ||
D. The absorbance will be quartered. | ||
E. There is no way to tell, because concentration and absorbance are not a linear relationship. |
A. The relationship between absorbance and concentration is not linear at high concentrations. | ||
B. The detector will reach its detection threshhold. | ||
C. The photon source is too weak to provide accurate results. | ||
D. The molar absorptivity of a compound is dependent on its concentration. | ||
E. There is no need to work with dilute concentrations; any concentration will work. |
A. σ → σ* | ||
B. σ → n | ||
C. σ → π* | ||
D. n → π* |
A. σ → σ* absorbances | ||
B. σ → n absorbances | ||
C. σ* → π* absorbances | ||
D. π → π* absorbances | ||
E. Metal to ligand charge transfer (MLCT) absorbances |
A. Detector, sample, source, monochromator | ||
B. Source, monochromator, sample, detector | ||
C. Source, sample, monochromator, detector | ||
D. Monochromator, source, sample, detector | ||
E. Sample, source, monochromator, detector |
A. To remove stray light from the room | ||
B. To serve as a polychromatic light source | ||
C. To interpret the photon signal into a digital readout | ||
D. To allow only light of a certain wavelength to pass from the source to the sample | ||
E. To focus light from the sample onto the detector |
The regression line from a plot of absorbance vs. concentration yields: A = 2.31 c + 0.002. If the absorbance of an unknown is measured to be 0.124, what is the concentration of the analyte?
A. 0.29 M | ||
B. 0.053 M | ||
C. 1.86 M | ||
D. 0.093 M | ||
E. 2.43 M |
A. The concentration at which the detector can no longer respond to the signal | ||
B. The mole ratio between the metal and ligand in a complex | ||
C. The maximum intensity of source photons transmitted | ||
D. The number of dimeric molecules formed | ||
E. The oxidation number of the metal |
A. Core electrons | ||
B. Valence electrons | ||
C. Nuclear spin | ||
D. Molecular vibrations | ||
E. Molecular rotations |
A. Core electrons | ||
B. Valence electrons | ||
C. Molecular vibrations | ||
D. Molecular rotations | ||
E. Nuclear spin |
A. In-plane rocking. | ||
B. In-plane scissoring. | ||
C. Assymetric stretching. | ||
D. Out-of-plane twisting. | ||
E. Out-of-plane wagging. |
A. Aquesous samples can be measured; AgCl is not water soluble. | ||
B. There is no advantage. | ||
C. Silver chloride does not absorb IR radiation. | ||
D. Silver chloride is translucent. | ||
E. Sodium chloride is less expensive. |
A. A change in polarizability | ||
B. A change in dipole moment | ||
C. Emission of an electron | ||
D. Transfer of an electon | ||
E. Metal-ligand charge transfer |
A. The Nernst glower. | ||
B. The Globar source. | ||
C. An incandescent wire. | ||
D. A pyroelectric glower. |
A. A charge-coupled diode. | ||
B. A thermocouple. | ||
C. A pyroelectric detector. | ||
D. A photoelectric detector. |
A. Nuclear spin | ||
B. Valence electrons | ||
C. Core electrons | ||
D. Molecular vibrations | ||
E. Molecular rotations |
A. A doublet, with a peak integration of 2 | ||
B. A doublet, with a peak integration of 3 | ||
C. A triplet, with a peak integration of 2 | ||
D. A triplet, with a peak integration of 3 | ||
E. A single peak, with an integration of 5 |
A. It occurs between neighboring nuclei with identical frequencies but different quantum states via energy transfer. | ||
B. It occurs between the excited nuclei and nuclei within the sample matrix. | ||
C. It occurs between atoms in the same molecule. | ||
D. It occurs between the nuclei of the sample and the signal source. | ||
E. All of the above |
A. The amount of shielding | ||
B. The applied magnetic field | ||
C. The identity of the reference sample | ||
D. The electronegativity of the nucleus | ||
E. All of the above |
A. Relaxation from a singlet excited state to a singlet ground state | ||
B. Relaxation from a triplet excited state to a singlet ground state | ||
C. Nonradiative (vibrational) relaxation | ||
D. Intersystem crossing (isc) | ||
E. All of the above |
A. Relaxation from a singlet excited state to the singlet ground state | ||
B. From a triplet excited state to the singlet ground state | ||
C. Intersystem crossing (isc) | ||
D. Nonradiative (vibrational) relaxation | ||
E. All of the above |
A. To ensure that incident (source) photons are not observed | ||
B. Because the sample cell is darkened on two adjacent sides | ||
C. Because the monochromator directs the light at a 90 degree angle | ||
D. Because the process of fluorescence and phosphorescence are too intense to observe directly | ||
E. To make the overall instrument smaller |
A. Vitamins. | ||
B. Environmental pollutants. | ||
C. Uncomplexed metal ions. | ||
D. Pharmaceuticals. | ||
E. Aromatic amino acids. |
A. Returning to the ground state by fluorescence | ||
B. Returning to the ground state by non-radiative decay | ||
C. Returning to the ground state by intersystem crossing | ||
D. Remaining in the excited state past the experimental timeframe | ||
E. None of the above |
A. Because the photon sources are too weak to vibrationally excite the samples | ||
B. Because sample cells are small | ||
C. Because they supply a reference signal | ||
D. Because fluorescence intensities are usually low | ||
E. None of the above |
A. Phosphorescence is more likely to coccur at low temperatures in a viscous medium. | ||
B. Phosphorescent molecules tend to also have explosive properties. | ||
C. The monochromator slows down the radiation before it hits the sample. | ||
D. The detector requires lower temperatures for operation. | ||
E. The source radiation can overheat and destory the analyte. |
A. Turbidimerty measures the decrease in transmittance of incident radiation; nephelometry measures the intensity of scattered radiation. | ||
B. Nephelometry measures the decrease in transmittance of incident radiation; turbidimetry measures the intensity of scattered radiation. | ||
C. Nephelometry measures the total metal ion, or inorganic, content; turbidimetry measures total organic content. | ||
D. Turbidimetry measures the total metal ion, or inorganic, content; nephelometry measures total organic content. | ||
E. The terms are synonymous; there is no difference. |
A. Light scattering | ||
B. Photon emission | ||
C. Photon absorption | ||
D. Nuclear repulsion | ||
E. Paramagnetism |
A. Better atomiza higher population of excited statestion and a | ||
B. Lower operating temperatures and less expensive replacement costs | ||
C. Minimization of scattering and ionization of analytes | ||
D. All of the above | ||
E. None of the above |
A. The small amount of analyte that actually reaches the flame | ||
B. The high temperatures of analysis often destroy the atoms | ||
C. The amount of dilution due to mixing with large volumes of combustion gases | ||
D. A and B only | ||
E. A and C only |
A. Linear | ||
B. Exponential | ||
C. Parabolic | ||
D. Polynomial | ||
E. Asymptopic |
A. Solid phase | ||
B. Liquid (neat) phase | ||
C. Gas phase | ||
D. Aquesous phase | ||
E. Plasma phase |
A. Because cathode lamps are cheaper to operate and maintain | ||
B. Because continuous spectrum lamps do not emit at the proper intensity | ||
C. Because the width of an atom's absorption band is narrow | ||
D. Because continuous spectrum lamps cause ionization of the molecules | ||
E. All of the above |
A. Ionization of the analyte | ||
B. Scattering and absorption by the matrix of the analyte | ||
C. Reactions between the analyte and matrix | ||
D. Non-volatilization of the analyte |
A. Nonvolatilization of the analyte | ||
B. Ionization of the analyte | ||
C. Absorption or scattering of radiation by the matrix | ||
D. All of the above | ||
E. A and B only |
A. Intersystem crossing | ||
B. Internal conversion | ||
C. External conversion | ||
D. Vibrational relaxation | ||
E. All of the above |
A. When a molecule transfers to a higher vibrational energy level of a lower energy electronic state with a different spin | ||
B. When a molecule moves to a lower vibrational energy level in the same electronic state | ||
C. When a molecule transfers to a higher vibrational energy level of a lower energy electronic state with the same spin | ||
D. energy is emitted as a photon from a singlet or triplet spin state | ||
E. When energy is passed to the solvent or to another component of the sample's matrix |
A. Ground state | ||
B. Zero state | ||
C. Newtonian state | ||
D. Bohring state | ||
E. Non-excited state |
A. Its spin-pairing with the ground state | ||
B. The amount of radiation it was exposed to | ||
C. Its ability to undergo radiationless decay | ||
D. Its initial energy level before absorption | ||
E. Its availability to become excited |
A. Yes, 0.54 | ||
B. No, 0.54 | ||
C. Yes, 1.09 | ||
D. No, 1.09 | ||
E. There is not enough information given to determine resolution. |
A. Components that had no interaction with the stationary phase | ||
B. The peak that arises from poor selection of a stationary phase | ||
C. The peak that arises from the mobile phase only | ||
D. Components that had no interaction with the mobile phase | ||
E. All peaks after the first peak in the chromatogram |
A. 1.8 mm/plate | ||
B. 15 mm/plate | ||
C. 29 mm/plate | ||
D. 0.24 mm/plate | ||
E. 2.7 mm/plate |
A. Columns containing more theoretical plates make separations imposssible. | ||
B. Columns containing more theoretical plates take a long time to perform separations. | ||
C. Columns containing more theoretical plates are better suited to separate a complex mixture. | ||
D. Columns containing more theoretical plates interact irreversibly with the analyte. | ||
E. Columns containing more theoretical plates lend themselves to component mixing. |
A. Interactions of the solute with the stationary phase | ||
B. Overloading the column with sample | ||
C. Interactions between the stationary and mobile phases | ||
D. Too many theoretical plates | ||
E. Small theortetical plate heights |
"Fronting" of a chromatographic peak is a result of which of the following?
A. Interactions between the stationary and mobile phase | ||
B. Overloading the column with sample | ||
C. Interactions of the solute with the stationary phase | ||
D. Small theortetical plate heights |
A. Mass transfer in the stationary phase | ||
B. Mass transfer in the mobile phase | ||
C. Longitudinal diffusion | ||
D. Variations in path lengths (Eddy diffusion) | ||
E. All of the above |
A. Oxygen. | ||
B. Nitrogen. | ||
C. Helium. | ||
D. Argon. | ||
E. Carbon dioxide. |
A. When the samples are injected slowly and in large quantities | ||
B. When the samples are injected slowly and in small quantities | ||
C. When the samples are injected quickly and in large quantities | ||
D. When the samples are injected quickly and in small quantities | ||
E. None of the above |
A. Silica gel | ||
B. Alumina | ||
C. Fused silica | ||
D. Glass | ||
E. Diatomaceous earth |
A. Open tubular GC columns | ||
B. Capillary GC columns | ||
C. Packed GC columns | ||
D. Both A and B | ||
E. Both A and C |
A. Flame ionization detector (FID) | ||
B. Thermal conductivity detector (TCD) | ||
C. Flame photometric detector (FPD) | ||
D. Hall electrolytic conductivity detector | ||
E. Nitrogen-phosphorus detector |
A. Thermal conductivity detector (TCD) | ||
B. Electron capture detector (ECD) | ||
C. Photoionization detector (PID) | ||
D. Flame photometric detector (FPD) | ||
E. None of these detectors would be affected by the carrier gas. |
A. They elude first, before smaller particles. | ||
B. They are broken down into smaller particles. | ||
C. They become oxidized as they move through the column. | ||
D. They remain on the column longer than smaller particles. | ||
E. They bind permanently to the stationary phase. |
A. Hydrophilic molecules | ||
B. Hydrophobic molecules | ||
C. Mixed metal sulfides and oxides | ||
D. Large molecules, such as DNA and RNA | ||
E. Cations and anions |
A. It requires lower pressures than those needed for HPLC. | ||
B. It gives better resolution than GC. | ||
C. It has densities similar to a liquid. | ||
D. Its mobile phase has the viscosity properties of a gas. | ||
E. It has solvent properties of a liquid. |
A. Sulfonic acid (-SO3-) | ||
B. Carboxylic acid (-COO-) | ||
C. Quarternary amine (-CH2N(CH3)3+) | ||
D. Amine (-NH3+) | ||
E. Hydroxyl (-OH-) |
A. A stationary phase and mobile phase of similar polarities | ||
B. A nonpolar stationary phase and a nonpolar mobile phase | ||
C. A polar stationary phase and a nonpolar mobile phase | ||
D. A nonpolar stationary phase and a polar mobile phase | ||
E. A polar stationary phase and a polar mobile phase |
A. Ca2+ | ||
B. CH3NH3+ | ||
C. Cl- | ||
D. HCOO- | ||
E. CH3COO- |
A. Via applying an electric current | ||
B. Via saponification of the analyte | ||
C. Via polymerization of the analyte | ||
D. Via oxidation reactions at stationary phase sites | ||
E. Via reduction reactions at stationary phase sites |
A. Metallic electrode of the second kind | ||
B. Metallic electrode of the first kind | ||
C. Saturated calomel electrode | ||
D. Reference electrode | ||
E. Silver/silver chloride electrode |
a. Saturated calomel electrode | ||
b. Metallic electrode of the first kind | ||
c. Metallic electrode of the second kind | ||
d. Silver/silver chloride electrode | ||
e. Reference electrode |
A. Oxidation | ||
B. Reduction | ||
C. Transference | ||
D. Sublimation | ||
E. Neutralization |
A. Oxidation | ||
B. Reduction | ||
C. Sublimation | ||
D. Transference | ||
E. Neutralization |
A. Cationic species | ||
B. Anionic species | ||
C. Neutral species | ||
D. Reducing agent | ||
E. Oxidizing agent |
A. Oxidizing agent | ||
B. Reducing agent | ||
C. Cationic species | ||
D. Anionic species | ||
E. Neutral species |
A. To complete the electrochemical circuit | ||
B. To provide free electrons for redox processes | ||
C. To provide a site for oxidative reduction | ||
D. To serve as a working electrode | ||
E. To serve as a reference electrode |
A. The current is zero, and the potential is given by the Nernst equation. | ||
B. The current and potential are both zero. | ||
C. The current is negative, and the potential is zero. | ||
D. The current is positive, and the potential is zero. | ||
E. The potential is zero, and the current is given by the Nernst equation. |
A. Measure the potential at zero current. | ||
B. Measure the potential while controlling the current. | ||
C. Measure the potential and current simultaneously. | ||
D. Measure the current while controlling the potential. | ||
E. All of the above |
A. Potentiometry | ||
B. Controlled-current coulometry | ||
C. Controlled-potential coulometry | ||
D. Cyclic voltammetry | ||
E. Amperometry |
A. At the anode | ||
B. At the cathode | ||
C. Within the potentiometer | ||
D. Within the salt bridge | ||
E. Within the bulk solution |
A. Within the potentiometer | ||
B. Within the salt bridge | ||
C. At the anode | ||
D. At the cathode | ||
E. Within the bulk solution |
A. Matrix effects | ||
B. Temperature effects | ||
C. Junction potentials | ||
D. All of the above | ||
E. None of the above |
A. Osmotic | ||
B. Bridging | ||
C. Coulombic | ||
D. Reference | ||
E. Junction |
A. These electrodes combine to make a complete electrochemical cell. | ||
B. These electrodes are typically used as reference electrodes. | ||
C. These electrodes are typically used as working (indicator) electrodes. | ||
D. These electrodes are examples of membrane electrodes. | ||
E. These electrodes have the same electrochemical potential. |
A. Glass ion selective electrode | ||
B. Potentiometric biosensor (enzyme electrode) | ||
C. Solid-state ion selective electrode | ||
D. Liquid-based ion selective electrode | ||
E. Gas-sensing electrode |
A. The concentration of anayte | ||
B. The surface area of the working electrode | ||
C. The number of electrons involved in the redox process | ||
D. The diffusion coefficient of the electroactive species | ||
E. All of the above |
A. Hydrodynamic voltammetry | ||
B. Stripping voltammetry | ||
C. Amperometry | ||
D. Polarography | ||
E. Cyclic voltammetry |
A. Type of working electrode | ||
B. How the potential is applied | ||
C. The inclusion of convection | ||
D. How the current is applied | ||
E. All of the above |
A. Current versus time | ||
B. Electrochemical potential versus time | ||
C. Current versus electrochemical potential | ||
D. Current only | ||
E. Potential only |