|
a. A mirror plane combined with an inversion |
||
|
b. Two proper rotation axes combined |
||
|
c. Identity combined with a mirror plane |
||
|
d. A proper rotation axis combined with a mirror plane |
||
|
e. The combination of two mirror planes |
|
a. Polarizability, dipole moment |
||
|
b. Magnetism, dipole moment |
||
|
c. Symmetry, magnetism |
||
|
d. Dipole moment, polarizability |
||
|
e. Magnetism, symmetry |
|
a. E |
||
|
b. C5 |
||
|
c. i |
||
|
d. S10 |
||
|
e. C6 |
|
a. IR active only |
||
|
b. Raman active only |
||
|
c. Both IR and Raman active |
||
|
d. Neither IR or Raman active |
||
|
e. The only spectroscopically active mode in the molecule |
|
a. IR active only |
||
|
b. Raman active only |
||
|
c. Both IR and Raman active |
||
|
d. Neither IR or Raman active |
||
|
e. The only spectroscopically active mode in the molecule |
|
a. Both the electronic and vibrational representations must be symmetric. |
||
|
b. Both the electronic and vibrational representations must be asymmetric. |
||
|
c. Only the electronic representations must be symmetric. |
||
|
d. Only the vibrational representations must be symmetric. |
||
|
e. Symmetry does not matter, as long as there is a change in dipole or polarizability. |
|
a. Closure (If A and B belong to the group, and A x B = C, then C also belongs to the group.) |
||
|
b. Associativity (A(BC) = (AB)C ) |
||
|
c. Identity (The symmetry element times its identity, E, remains unchanged.) |
||
|
d. Inverses (There must be an inverse symmetry element that returns the molecule to its original state; A x A-1 = E.) |
||
|
e. Continuity (If a molecule contains an n axis, then it also contains axes of n-1, n-2...) |
|
a. D2d |
||
|
b. Cs |
||
|
c. C2h |
||
|
d. S4 |
||
|
e. D4 |
|
a. H2O |
||
|
b. BrF5 |
||
|
c. BH3 |
||
|
d. PCl6 |
||
|
e. W(CO)6 |
|
a. SF6 |
||
|
b. O2 |
||
|
c. BF3 |
||
|
d. C2Cl4 |
||
|
e. All of the above |
|
a. Helium also has electrons in antibonding orbitals, resulting in a bond order of zero. |
||
|
b. Helium also has electrons in non-bonding orbitals, resulting in a bond order of zero. |
||
|
c. Helium is a noble gas and never forms bonds. |
||
|
d. Hydrogen also has electrons in nonbonding orbitals, resulting in a bond order of two. |
||
|
e. Hydrogen has no antibonding orbitals, resulting in a bond order of two. |
|
a. The amount of magnetic character is reduced in bonds. |
||
|
b. The electrons are shared between two elements. |
||
|
c. Nonbonding electrons decrease bond ability. |
||
|
d. The antibonding electrons interfere with bonding. |
||
|
e. None of the above |
|
a. 5 |
||
|
b. 1 |
||
|
c. 1.5 |
||
|
d. 2 |
||
|
e. 3 |
|
a. They should be at the same energy to indicate bond formation. |
||
|
b. They should be at the same energy to indicate allowed symmetry. |
||
|
c. They should be at different energies, relative to their difference in electronegativities. |
||
|
d. They should be at different energies, relative to their atomic radii. |
||
|
e. They should be at different energies, relative to the number of lone pairs of electrons. |
|
a. A maximum of two electrons per orbital is allowed. |
||
|
b. The orbitals with the lowest energy are filled first. |
||
|
c. Orbitals of the same energies are half-filled first; then electrons are allowed to pair up. |
||
|
d. Non-bonding orbitals are filled first. |
||
|
e. All of the above |
|
a. Nonbonding molecular orbitals |
||
|
b. Antibonding molecular orbitals |
||
|
c. Bonding molecular orbitals |
||
|
d. All of the above |
||
|
e. A and C only |
|
a. They must have constructive net interaction. |
||
|
b. They must have the correct symmetry to overlap |
||
|
c. They must be similar in energy |
||
|
d. There will be the same number of resultant molecular orbitals as atomic orbitals |
||
|
e. All of the above |
|
a. Sigma interactions occur along the internuclear axis. |
||
|
b. Pi interactions occur above and below the internuclear axis. |
||
|
c. Sigma bonds form first, followed by the subsequent formation of pi bonds. |
||
|
d. Two pi bonds are involved in a double bond. |
||
|
e. All of the above |
|
a. They are responsible for the formation of pi bonds. |
||
|
b. They are similar in energy to the atomic orbitals. |
||
|
c. They counteract bond formation in a molecule. |
||
|
d. They help hold the molecule together, once it is formed. |
||
|
e. They are responsible for the formation of sigma bonds. |
|
a. CO2 |
||
|
b. H2O |
||
|
c. CN- |
||
|
d. Cl2 |
||
|
e. N2 |
|
a. Mn2+ |
||
|
b. V |
||
|
c. Fe3+ |
||
|
d. All of the above |
||
|
e. A and C only |
|
a. An EPR spectrum shows that oxygen is paramagnetic; MO theory is correct. |
||
|
b. An EPR spectrum shows that oxygen is paramagnetic; VBT is correct. |
||
|
c. Infrared spectroscopy shows a double bond stretch; MO theory is correct. |
||
|
d. Infrared spectroscopy shows a double bond stretch; VBT is correct. |
||
|
e. There is no way to know which theory is correct in this matter. |
|
a. There is no actual difference; the orbitals involved are the same, only listed in a different order. |
||
|
b. The complex having d2sp3 hybridization is an “inner shell” complex, while the complex with sp3d2 hybridization is an “outer shell” complex. |
||
|
c. The complex having d2sp3 hybridization is an “outer shell” complex, while the complex with sp3d2 hybridization is an “inner shell” complex. |
||
|
d. The complex having sp3d2 hybridization does not exist; the electrons must fill the lowest energy orbitals first. |
||
|
e. The complex having d2sp3d2 hybridization does not exist; the electrons must fill the orbitals with the same principle quantum number. |
|
a. Octahedral |
||
|
b. Tetrahedral |
||
|
c. Square planar |
||
|
d. All of the above |
||
|
e. Both A and C |
|
a. They increase their ionization potential, rendering them most useful electrochemically. |
||
|
b. They reduce degenerate molecular orbitals, allowing a more stable molecule to exist. |
||
|
c. They undergo a strong magnetic transition, allowing easier detection by NMR and EPR. |
||
|
d. They increase their transition state energy, making them useful catalysts. |
||
|
e. They decrease shielding, allowing spectroscopically forbidden transitions to occur. |
|
a. Yes. The five electrons distribute themselves evenly in the five molecular orbitals, causing them to be degenerate. Axial elongation reduces this degeneracy. |
||
|
b. Yes. The five electrons distribute themselves evenly in the five molecular orbitals, causing them to be degenerate. Axial compression reduces this degeneracy. |
||
|
c. No. The five electrons distribute themselves evenly in the five molecular orbitals; no degeneracy exists. |
||
|
d. No. Four of the electrons are paired. Only one electron is unpaired and can only fill the one remaining orbital. No degeneracy exists. |
||
|
e. Yes. Four electrons are paired in the lower energy orbitals. The fifth electron can position itself into any of the remaining three orbitals, making it triply degenerate. |
|
a. mer-bis(cyclopentadienyl)iron(II) |
||
|
b. fac-bis(cyclopentadienyl)iron(II) |
||
|
c. bis(η5-cyclopentadienyl)iron(II) |
||
|
d. µ-bis(cyclopentadienyl)iron(II) |
||
|
e. (η5-cyclopentadienyl)iron(II) |
|
a. One would be a solid at room temperature, while the other would be a liquid. |
||
|
b. One would be highly colored, while the other would be colorless. |
||
|
c. One would be paramagnetic, while the other would be diamagnetic. |
||
|
d. One would rotate plane-polarized light clockwise, while the other would rotate it counterclockwise. |
||
|
e. All of the above |
|
a. Because the stability gained from having a fully-filled or evenly, half-filled set of d orbitals is greater than the need to fill all lower energy orbitals first |
||
|
b. Because the 3d orbital is actually lower in energy than the 4s, so it fills first |
||
|
c. Because copper and chromium only exist as ions; never as neutral elements |
||
|
d. Because the atomic radii are so large that no effect is felt by the nucleus |
||
|
e. None of the above |
|
a. mu (µ) |
||
|
b. eta (η) |
||
|
c. chi (χ) |
||
|
d. xi (ξ) |
||
|
e. zeta (ζ) |
|
a. They are malleable and ductile. |
||
|
b. They have high melting points. |
||
|
c. They conduct heat and electricity. |
||
|
d. They are lustrous. |
||
|
e. They undergo irreversible oxidation. |
|
a. A low spin, d5 octahedral complex |
||
|
b. A high spin, d8 octahedral complex |
||
|
c. A low spin, d3 octahedral complex |
||
|
d. A d2 tetrahedral complex |
||
|
e. A d5 square planar complex |
|
a. Fe(CO)5 |
||
|
b. Ni(CO)5 |
||
|
c. Mo(CO)6 |
||
|
d. Re(CO)6 |
||
|
e. Ir(CO)5 |
|
a. The result is a low-spin complex, where electrons will pair up and fill the lowest energy level. |
||
|
b. The result is a high-spin complex, where electrons will be promoted to the next energy level before pairing. |
||
|
c. The result is an unstable complex, where electrons can either pair or be promoted to the next energy level. |
||
|
d. The result is a high-spin complex, where electrons will pair up and fill the lowest energy level. |
||
|
e. The result is a low-spin complex, where electrons will be promoted to the next energy level before pairing. |
|
a. BF3 |
||
|
b. ClF3 |
||
|
c. PF6 |
||
|
d. IF5 |
||
|
e. SbF5 |
|
a. Charge of the metal ion |
||
|
b. Nature of the ligands |
||
|
c. Geometry of the complex |
||
|
d. Size of the ligands |
||
|
e. All of the above |
|
a. [PtCl(H2O)3]Br and [Pt(Br)(H2O)3]Cl |
||
|
b. cis-[PtCl2(NH3)2] and trans-[PtCl2(NH3)2] |
||
|
c. [CrCl2(H2O)4]Cl•2H2O and [CrCl3(H2O)3]•3H2O |
||
|
d. [Co(NH3)6] [Cr(ac)3] and [Co(ac)3] [Cr(NH3)6] |
||
|
e. [Co(SCN)(NH3)5]- and [Co(NCS)(NH3)5]- |
|
a. Copper |
||
|
b. Iron |
||
|
c. Gold |
||
|
d. Titanium |
||
|
e. Tungsten |
|
a. It is highly polarizable. |
||
|
b. The ligand is relatively large. |
||
|
c. The ligand exhibits π donor ability. |
||
|
d. The ligand is acidic. |
||
|
e. All of the above |
|
a. Silver |
||
|
b. Rhodium |
||
|
c. Cadmium |
||
|
d. Molybdenum |
||
|
e. The melting points would be equivalent, because they are in the same period. |
|
a. Violet |
||
|
b. Blue |
||
|
c. Green |
||
|
d. Yellow |
||
|
e. Red |
|
a. Jahn-Teller distortion |
||
|
b. Mixing of the p and d orbitals |
||
|
c. MLCT |
||
|
d. LMCT |
||
|
e. All of the above |
|
a. The spectrum would show one very broad absorption band at 533 nm. |
||
|
b. The spectrum would show two weak absorption bands, one at 412 nm and the other at 654 nm. |
||
|
c. The spectrum would show two strong absorption bands, one at 412 nm and the other at 654 nm. |
||
|
d. The spectrum would show two weak absorption bands, one at 472 nm and the other at 594 nm. |
||
|
e. The spectrum would show two strong absorption bands, one at 472 nm and the other at 594 nm. |
|
a. The ligand field stabilization energy (LFSE) is insufficient to allow transitions to the left of the line. |
||
|
b. The transitions to the left are symmetry allowed, while the transitions to the right are spin allowed. |
||
|
c. The transitions to the left are spin allowed, while the transitions to the right are symmetry allowed. |
||
|
d. The transitions to the left are low-spin complexes, while the transitions to the right are high-spin complexes. |
||
|
e. The transitions to the left are high-spin complexes, while the transitions to the right are low-spin complexes. |
|
a. Two |
||
|
b. Three |
||
|
c. Nine |
||
|
d. Six |
||
|
e. Zero |
|
a. CT absorptions occur at higher wavelengths than d-d transitions. |
||
|
b. CT absorptions are less intense than d-d transitions. |
||
|
c. CT transitions are symmetry and spin allowed; d-d transitions are symmetry forbidden. |
||
|
d. CT transitions are spin allowed; d-d transitions are spin forbidden. |
||
|
e. CT transitions are symmetry and spin forbidden; d-d transitions are symmetry forbidden but spin allowed. |
|
a. Zn2+ has a completely filled d orbital, and Sc3+ has a completely empty d orbital. |
||
|
b. Zn2+ and Sc3+ always form high spin octahedral complexes. |
||
|
c. Zn2+ and Sc3+ always form low spin octahedral complexes. |
||
|
d. Zn2+ and Sc3+ are diamagnetic; the others are paramagnetic. |
||
|
e. Zn2+ and Sc3+ are paramagnetic; the others are diamagnetic. |
|
a. The transition in the high spin complex is symmetry and spin forbidden. The transition in the low spin complex is symmetry allowed. |
||
|
b. The transition in the high spin complex is symmetry and spin forbidden. The transition in the low spin complex is spin allowed. |
||
|
c. The transition in the high spin complex is symmetry forbidden but spin allowed. The transition in the low spin complex is symmetry and spin allowed. |
||
|
d. The transition in the high spin complex is spin forbidden but symmetry allowed. The transition in the low spin complex is symmetry and spin allowed. |
||
|
e. The transition in the high spin complex is symmetry and spin forbidden. The transition in the low spin complex is symmetry and spin allowed. |
|
a. The solution containing cyanide ion will give a larger crystal field splitting, causing a blue shift in the color of the complex. The complex with thiocyanate ion will appear as more red shifted. |
||
|
b. The solution containing cyanide ion will give a smaller crystal field splitting, causing a blue shift in the color of the complex. The complex with thiocyanate ion will appear as more red shifted. |
||
|
c. The solution containing cyanide ion will give a larger crystal field splitting, causing a red shift in the color of the complex. The complex with thiocyanate ion will appear as more blue shifted. |
||
|
d. The solutions will both be similar in color; however, the complex with thiocyanate will be more intense. |
||
|
e. You cannot tell them apart; the experiment would need to be restarted. |
|
a. Dynamic fluxionality |
||
|
b. Spin-spin coupling interactions |
||
|
c. Integer quantum spin numbers (I = 1,2,3…) |
||
|
d. Fractional quantum spin numbers (I = 1/2, 3/2, 5/2) |
||
|
e. Low natural abundances of the 19F nucleus |
|
a. The asymmetric stretch of the C-O bonds creates a dipole moment that is IR active. |
||
|
b. The symmetric stretch of the C-O bonds creates a dipole moment that is IR active. |
||
|
c. The non-linear bending mode crates a net dipole, which is IR active. |
||
|
d. All of the above |
||
|
e. A and C only |
|
a. The chemical shift and resonance frequency also change. |
||
|
b. The chemical shift changes; the resonance frequency remains constant. |
||
|
c. The chemical shift remains constant; the resonance frequency changes. |
||
|
d. The chemical shift and resonance frequency remain constant. |
||
|
e. There is no way to predict the effect. |
|
a. The Zeeman effect |
||
|
b. Pauli exclusion principle |
||
|
c. Symmetry degeneracy |
||
|
d. Fermi contact interaction |
||
|
e. Bose-Einstein effect |
|
a. Dissociation and recoordination of the carbonyl ligands |
||
|
b. Rotation of a hindered carbonyl bond |
||
|
c. Opening and closing of bridging carbonyls |
||
|
d. Isomerism between trigonal bipyramidal and square pyramidal configurations |
||
|
e. Monmer-dimer formation with a bridging carbonyl |
|
a. NO2 radical |
||
|
b. CH3 radical |
||
|
c. CH2Cl radical |
||
|
d. CH2CH2 radical |
||
|
e. OH radical |
|
a. Paramagnetic transition metal complexes |
||
|
b. Diamagnetic transition metal complexes |
||
|
c. Free radicals in the solid state |
||
|
d. Free radicals in the liquid or gas state |
||
|
e. Complexes containing more than one unpaired electron |
|
a. An odd mass number and odd atomic number, such as 1H |
||
|
b. An odd mass number and an even atomic number, such as 13C |
||
|
c. An even mass number and an even atomic number, such as 16O |
||
|
d. An even mass number and an odd atomic number, such as 14N |
||
|
e. All of the above situations will result in a nonzero quantum spin number. |
|
a. A free electron |
||
|
b. An unpaired electron in an organic molecule |
||
|
c. An unpaired electron in a transition metal complex |
||
|
d. All of the above |
||
|
e. A and B only |
|
a. Cationic metal complexes experience less π backbonding than their neutral or anionic analogs. |
||
|
b. Pyridine is a good π acceptor and contributes to increased π backbonding. |
||
|
c. The carbonyl to metal bond strength is increased in the chloro complex. |
||
|
d. All of the above |
||
|
e. A and B only |
|
a. Two; through the lone pairs on the two nitrogen atoms |
||
|
b. Two; through the lone pairs on two of the oxygen atoms |
||
|
c. Four; through the lone pairs on the four oxygen atoms |
||
|
d. Four; through the anion on the four oxygen atoms |
||
|
e. Six; two through the lone pairs on the two nitrogen atoms and four through the lone pairs of the four oxygen atoms |
|
a. Associative mechanism, aided by a ring slip |
||
|
b. Dissociative mechanism, in which the Cp ring is lost |
||
|
c. Inversion of stereochemistry and loss of the Cp ring |
||
|
d. Dissociation of the Cp ligand, followed by re-association of Cp |
||
|
e. All of the above |
|
a. It is dependent on which ligands are a part of the primary valence and which ones are a part of the secondary valence. |
||
|
b. It depends on the charge of the metal ion present. |
||
|
c. It depends on the number of empty d orbitals. |
||
|
d. It depends on the nature of the ligands involved and whether they are mono or multi-dentate. |
||
|
e. All of the above |
|
a. 2 |
||
|
b. 5 |
||
|
c. 6 |
||
|
d. 8 |
||
|
e. 10 |
|
a. 2 |
||
|
b. 3 |
||
|
c. 4 |
||
|
d. 5 |
||
|
e. 6 |
|
a. +3 |
||
|
b. +2 |
||
|
c. +4 |
||
|
d. +7 |
||
|
e. +6 |
|
a. It plays an important role in insertion, polymerization, and metathesis reactions. |
||
|
b. It describes a complex with a coordination number less than 4. |
||
|
c. It generally means another ligand can be accommodated. |
||
|
d. All of the above |
||
|
e. A and C only |
|
a. [Co(Cl3)](NH3)6; AgCl is formed. |
||
|
b. [Co(Cl3)](NH3)6; NH4Cl is formed. |
||
|
c. [Co(NH3)6]Cl3; AgCl is formed. |
||
|
d. [Co(NH3)6]Cl3; NH4Cl is formed. |
||
|
e. Both will react with silver in water; AgCl and NH4Cl are formed. |
|
a. EDTA |
||
|
b. SCN- |
||
|
c. NH3 |
||
|
d. Hemoglobin |
||
|
e. Cl- |
|
a. Hydrophilic interactions |
||
|
b. Hydrophobic interactions |
||
|
c. Van der Waals interactions |
||
|
d. Lewis acid-base interactions |
||
|
e. Hydrogen bonding interactions |
|
a. Fe(s) |
||
|
b. Fe3+(aq) |
||
|
c. Fe(OH)2(s) |
||
|
d. Fe2+(aq) |
||
|
e. Fe(OH)3(s) |
|
a. The species on the left is readily reduced to the species on the right side of the arrow. |
||
|
b. The species on the lef tis a good reducing agent. |
||
|
c. The species under goes diproportionation. |
||
|
d. All of the above. |
||
|
e. None of the above. |
|
a. The heat of formation of the precursor complex |
||
|
b. The heat of fission of the successor complex |
||
|
c. The solvation energy of the transition complex |
||
|
d. The free energy of electron transfer |
||
|
e. All of the above |
|
a. The reaction does not proceed. |
||
|
b. The reaction is drastically slowed, requiring a spin flip to occur. |
||
|
c. The reaction proceeds quicker, because different spin states allow faster electron transfer. |
||
|
d. The reaction will proceed as inner sphere instead, because electrons with different spin will pair and form a bond. |
||
|
e. None of the above |
|
a. Even though a reaction is thermodynamically favorable, the reaction may be slow kinetically. |
||
|
b. All redox reactions are favorable at in alkaline media. |
||
|
c. All thermodynamically favorable reactions occur quickly on a kinetic scale. |
||
|
d. If a reaction is kinetically favorable, it will proceed even if it is thermodynamically unfavorable. |
||
|
e. No redox reactions occur in highly acidic media. |
|
a. Formation of the bridging ligand complex |
||
|
b. Formation of the precursor (cage) complex |
||
|
c. Electron transfer |
||
|
d. Solvent entering the coordination sphere |
||
|
e. Fission of the successor ligand complex |
|
a. Formation of the bridging ligand complex |
||
|
b. Fission of the successor ligand complex |
||
|
c. Electron transfer |
||
|
d. Solvent entering the coordination sphere |
||
|
e. Both B and C |
|
a. H3PO4 |
||
|
b. NH4+ |
||
|
c. HNO3 |
||
|
d. PH3 |
||
|
e. P & N (elemental) |
|
a. They experience Jahn-Teller distortion, making their axial bonds longer and easier to break. |
||
|
b. Their ground state structure resembles their transition state structure. |
||
|
c. Their electrons are distributed equally among the d-orbitals. |
||
|
d. Their large radii can accommodate a larger coordination sphere. |
||
|
e. Both A and B |
|
a. Tetragonal |
||
|
b. Trigonal bipyramidal |
||
|
c. Square pyramidal |
||
|
d. Both A and C |
||
|
e. All of the above |
|
a. The trans influence |
||
|
b. The trans effect |
||
|
c. The biphilic effect |
||
|
d. The solvolysis effect |
||
|
e. The anation effect |
|
a. Enthalpy of reaction |
||
|
b. Decreased activation energy |
||
|
c. Formation of dimeric species (bridging ligands) |
||
|
d. Entropy of reaction |
||
|
e. Outer sphere electron transfer |
|
a. The chloride ions are larger than the water molecules, only allowing four to coordinate around the central metal ion; ammonia is similar in size to water, so six will coordinate. |
||
|
b. The chloride ions are anionic, and the metal centers cannot accommodate a larger negative charge; ammonia is a neutral species. |
||
|
c. Chloride ions precipitate the metals out of solution; ammonia complexes do not. |
||
|
d. The addition of excess chloride ions will actually result in hexa-chloro compounds. |
||
|
e. Chloride additions occur in acidic media; ammonia is alkaline. |
|
a. The entering group |
||
|
b. The leaving group |
||
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c. Other ligands in the coordination sphere |
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d. The metal center itself |
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e. All of the above |
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a. It is a kinetic phenomenon. |
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b. It can influence M-L bond lengths. |
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c. It can result in changes in NMR coupling constants. |
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d. It can affect the vibrational frequency. |
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e. It is purely thermodynamic. |
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a. They occur via an associative mechanism with a five coordinate intermediate. |
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b. They only proceed when bond formation is the rate determining step. |
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c. They only proceed when bond breaking is the rate determining step. |
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d. They only proceed when the transition energies of bond formation and bond breaking are similar. |
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e. They occur via a dissociative mechanism with a three coordinate intermediate. |
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a. k = [A][B] |
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b. k = [A] |
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c. k = [A]2[B] |
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d. Both A and C |
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e. The mechanism cannot be determined from the rate law. |
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a. Activation energy |
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b. Thermal energy |
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c. Electron transfer |
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d. Entropy |
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e. Enthalpy |
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a. Ammonia |
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b. Sulfur trioxide |
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c. Sulfuric acid |
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d. Margarine |
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e. Nitric acid |
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a. Ammonia |
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b. Sulfur trioxide |
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c. Sulfuric acid |
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d. Margarine |
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e. Nitric acid |
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a. It shifts the equilibrium toward the products based on LeChatlier’s principle. |
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b. It provides an alternate route with a lower activation energy for the reaction to proceed. |
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c. It donates electrons to break or form bonds as needed until it is entirely consumed. |
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d. It forms bridging complexes which align the molecular orbitals of the reactants. |
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e. All of the above |
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a. The hydrogenation of vegetable oil in the presence of nickel to make margarine |
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b. The use of Pt, Pd or Rh in catalytic converters |
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c. The destruction of ozone in the atmosphere |
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d. The use of vanadium(V)oxide in the conversion of sulfur dioxide to sulfur trioxide |
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e. All of the above |
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a. Ru |
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b. Ti |
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c. V |
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d. Fe |
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e. All of the above |
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a. Doping allows the LED to harvest light from triplet states, increasing quantum efficiency. |
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b. Doping increases the overall number of singlet to singlet emission pathways. |
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c. It reduces the overall cost of producing an LED; the inorganic dopants are inexpensive. |
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d. All of the above |
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e. None of the above |
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a. Metal ion complexes are unable to harvest light energy. |
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b. The cost of the metal ion complexes is prohibitive. |
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c. The storage of energy occurs by thermal or chemical means. |
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d. The energy produced can only be utilized in electrical grids. |
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e. All of the above |
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a. Nickel-cadmium in portable electronics and toys |
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b. Lead acid batteries in automobiles |
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c. Silver-zinc button cells in hearing aides |
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d. Silver-cadmium batteries in satellites |
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e. Zinc-carbon dry cell batteries in flashlights |
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a. The organometallic complexes are easier to synthesize than the inorganic salts. |
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b. The organometallic complexes are less toxic and more effective in lowering blood glucose levels. |
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c. The organometallic complexes are less expensive to synthesize and cost less on the market. |
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d. The effect of the inorganic salts was discovered after the organometallic complexes had established a successful history. |
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e. The FDA will not approve medicinal use of purely inorganic compounds for biological applications. |
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a. Metals are nontoxic to humans. |
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b. Harmful stereoisomers do not exist. |
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c. They are soluble in water and easily administered. |
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d. They counteract drug resistance that has been built to purely organic molecules. |
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e. There are no current organometallic applications to antimicrobials. |