|
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 |
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E. Junction |
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A. These electrodes combine to make a complete electrochemical cell. |
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B. These electrodes are typically used as reference electrodes. |
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C. These electrodes are typically used as working (indicator) electrodes. |
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D. These electrodes are examples of membrane electrodes. |
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E. These electrodes have the same electrochemical potential. |
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A. Glass ion selective electrode |
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B. Potentiometric biosensor (enzyme electrode) |
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C. Solid-state ion selective electrode |
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D. Liquid-based ion selective electrode |
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E. Gas-sensing electrode |
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A. The concentration of anayte |
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B. The surface area of the working electrode |
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C. The number of electrons involved in the redox process |
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D. The diffusion coefficient of the electroactive species |
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E. All of the above |
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A. Hydrodynamic voltammetry |
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B. Stripping voltammetry |
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C. Amperometry |
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D. Polarography |
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E. Cyclic voltammetry |
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A. Type of working electrode |
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B. How the potential is applied |
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C. The inclusion of convection |
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D. How the current is applied |
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E. All of the above |
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A. Current versus time |
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B. Electrochemical potential versus time |
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C. Current versus electrochemical potential |
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D. Current only |
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E. Potential only |