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 ![]() |