a. 1 | ||
b. 3 | ||
c. 5 | ||
d. 7 |
a. 5d | ||
b. 6f | ||
c. 6p | ||
d. The subshell does not exist. |
a. is representative of a transition metal. | ||
b. is not allowed. | ||
c. is representative of a p-block element. | ||
d. is representative of an element with two valence electrons. |
a. xenon | ||
b. silicon | ||
c. gallium | ||
d. iodine |
a. boron trifluoride | ||
b. water | ||
c. carbon dioxide | ||
d. methane |
a. 2 | ||
b. 6 | ||
c. 10 | ||
d. 14 |
a. 2 | ||
b. 4 | ||
c. 8 | ||
d. 12 |
a. lithium. | ||
b. carbon. | ||
c. silicon. | ||
d. nitrogen. |
a. chlorine. | ||
b. argon. | ||
c. neon. | ||
d. boron. |
a. Moving from C to N adds an electron to an occupied orbital. | ||
b. The Zeff value for oxygen is raised due to additional shielding from fluorine. | ||
c. Moving from N to O pairs two electrons in a single orbital. | ||
d. The Zeff value decreases with an increase in electron repulsion. |
a. fluorine | ||
b. chlorine | ||
c. bromine | ||
d. iodine |
a. indium | ||
b. gallium | ||
c. boron | ||
d. aluminum |
a. RuNH33+ | ||
b. MnO4- | ||
c. CuNO3 | ||
d. Zn(ClO4)2 |
a. argon | ||
b. chlorine | ||
c. xenon | ||
d. bromine |
a. 2p | ||
b. 2s | ||
c. 3p | ||
d. 3s |
a. 1+ | ||
b. 1- | ||
c. 2+ | ||
d. There is no charge on the nitrogen. |
a. The sulfur disobeys the octet rule. | ||
b. Sulfur has more valence electrons than oxygen. | ||
c. Sulfur has a greater number of electron shells than oxygen. | ||
d. Sulfur is less electronegative than oxygen. |
a. H2O | ||
b. SF4 | ||
c. NH3 | ||
d. XeF4 |
a. square planar | ||
b. octahedral | ||
c. tetrahedral | ||
d. trigonal planar |
a. 0 | ||
b. 1 | ||
c. 2 | ||
d. 3 |
a. N2 | ||
b. C2 | ||
c. B2 | ||
d. Be2 |
a. high-spin iron(II) | ||
b. low-spin iron(II) | ||
c. high-spin iron(III) | ||
d. low-spin iron(III) |
a. water | ||
b. oxalic acid | ||
c. ammonia | ||
d. hydrobromic acid |
a. 2pσ | ||
b. 2pπ | ||
c. 2pσ* | ||
d. 2pπ* |
a. [Co(NH3)6]3-. | ||
b. [NiCl6]4-. | ||
c. [Ni(NH3)6]2+. | ||
d. [CoF6]3-. |
a. paramagnetic [FeCl6]3+. | ||
b. paramagnetic [Fe(CN)6]3+. | ||
c. diamagnetic [Co(NH3)6]3+. | ||
d. diamagnetic [CoF6]2+. |
a. K3[Rh(CN)6]. | ||
b. Na2[Rh(CN)6]. | ||
c. Na2[Rh(NH3)6]. | ||
d. K[Rh(CN)6]. |
a. amminetrichloroplatinate(II) ion. | ||
b. sodium amminetrichloroplatinate(II). | ||
c. sodium amminetrichloroplatinate(IV). | ||
d. potassium amminetrichloroplatinate(II). |
a. [Ni(CO)6]3+ | ||
b. [Ru(bipy)3]2+ | ||
c. [FeCl6]3+ | ||
d. [Co(CN)6]3- |
a. trigonal bipyrimidal | ||
b. tetragonal | ||
c. tetrahedral | ||
d. square planar |
a. a ≠b ≠c, α = β = γ = 90° | ||
b. a = b = c, α = β = γ ≠90° | ||
c. a = b = c, α = β = γ = 90° | ||
d. a ≠b ≠c, α = β = γ ≠90° |
a. base-centered orthorhombic | ||
b. face-centered cubic | ||
c. body-centered orthorhombic | ||
d. base-centered monoclinic |
a. 2 | ||
b. 4 | ||
c. 6 | ||
d. 8 |
a. Unlike crystalline solids, amorphous solids lack a repeating unit cell, leading to a random organization of atoms. | ||
b. Unlike crystalline solids, amorphous solids tend to lose structural organization as their lattices extend. | ||
c. Amorphous solids are said to behave as supercooled liquids, leading to an ease in transitioning between physical states. | ||
d. The formation of amorphous solids is aided by the rapid cooling of a molten compound. |
a. high melting point | ||
b. low electrical conductivity | ||
c. high level of hardness | ||
d. high water solubility |
a. 4 | ||
b. 6 | ||
c. 8 | ||
d. 14 |
a. 0 | ||
b. 1 | ||
c. 2 | ||
d. 4 |
a. fluorine | ||
b. chlorine | ||
c. bromine | ||
d. iodine |
a. selenium | ||
b. tellurium | ||
c. oxygen | ||
d. sulfur |
a. The unit cell is the simplest repeating unit in the crystal lattice. | ||
b. Opposing faces of a unit cell are parallel. | ||
c. Each unit cell edge is equivalent in length. | ||
d. Each unit cell edge connects equivalent points/atoms. |
a. -604 kJ/mol | ||
b. -660 kJ/mol | ||
c. -740 kJ/mol | ||
d. -819 kJ/mol |
a. Sodium has a larger ionic radius than cesium, allowing for less anion attraction. | ||
b. Due to its size, cesium makes more contact with adjacent anions than sodium does. | ||
c. The NaCl radius ratio is greater than that of CsCl, forcing anions farther from the metal cation. | ||
d. Chlorine is too electronegative to be completely compatible with sodium. |
a. 1 | ||
b. 4 | ||
c. 8 | ||
d. 12 |
a. 2 and 4 | ||
b. 4 and 2 | ||
c. 4 and 4 | ||
d. 6 and 4 |
a. perovskite | ||
b. NaCl | ||
c. rutile | ||
d. CsCl |
a. 14 | ||
b. 26 | ||
c. 74 | ||
d. 86 |
a. ABC | ||
b. AAA | ||
c. ABB | ||
d. ABA |
a. 4 | ||
b. 6 | ||
c. 8 | ||
d. 12 |
a. barium selenide | ||
b. beryllium oxide | ||
c. titanium(II) oxide | ||
d. strontium chloride |
a. 4. | ||
b. 6. | ||
c. 8. | ||
d. 12. |
a. 4 | ||
b. 6 | ||
c. 8 | ||
d. 12 |
a. 4 | ||
b. 6 | ||
c. 8 | ||
d. 12 |
a. 0.310 Ä | ||
b. 0.414 Ä | ||
c. 0.621 Ä | ||
d. 0.932 Ä |
a. 0.23 Ä | ||
b. 0.27 Ä | ||
c. 0.40 Ä | ||
d. 0.54 Ä |
a. There are at least three M spheres within the lattice. | ||
b. The lattice is body centered. | ||
c. The lattice is close-packed cubic. | ||
d. The system is hexacoordinate. |
a. 4. | ||
b. 6. | ||
c. 8. | ||
d. 10. |
a. pure metal. | ||
b. alkali metal. | ||
c. substitutional alloy. | ||
d. interstitial alloy. |
a. substitutional alloy, interstitial alloy | ||
b. intermetallic alloy, interstitial alloy | ||
c. substitutional alloy, intermetallic alloy | ||
d. pure metal, intermetallic alloy |
a. ease electron flow over band gaps. | ||
b. slow down the activity of the atom, promoting a gradual increase in conductivity. | ||
c. impede conductivity due to increased atom vibration. | ||
d. allow the metal to behave as a superconductor. |
a. Superconductors are perfectly paramagnetic. | ||
b. Most superconductors require low temperatures to be efficient. | ||
c. Superconductors exhibit high resistance to electron flow. | ||
d. Superconductors exhibit large energy gaps between the valence and conductor bands. |
a. has a limited number of electrons present. | ||
b. is often separated from the HOMO by an unsurmountable energy gap. | ||
c. serves as a dopant to the valence band. | ||
d. serves to provide electrons to the valence band. |
a. conductors. | ||
b. semiconductors. | ||
c. insulators. | ||
d. superconductors. |
a. conduction band electrons outnumber valence band holes. | ||
b. electron flow is halted due to dopant impurities. | ||
c. an equal number of valence band holes and conductor band electrons exist, making dopants unnecessary. | ||
d. doping is facilitated by halides. |
a. phosphorus | ||
b. boron | ||
c. antimony | ||
d. carbon |
a. Intrinsic superconductors require a dopant to conduct electricity. | ||
b. Semiconductors have no energy gap between the valence and conductor bands. | ||
c. Semiconductors increase in conductivity with increasing temperatures. | ||
d. Intrinsic semiconductors are more efficient than extrinsic semiconductors. |
a. LUMO, antibonding orbital | ||
b. LUMO, bonding orbital | ||
c. HOMO, nonbonding orbital | ||
d. HOMO, antibonding orbital |
a. valence band composition, with semiconductors and insulators having half- and fully filled HOMOs, respectively. | ||
b. electron placement, with electrons occupying the conductance bands of semiconductors but not of insulators. | ||
c. resistivity, with semiconductors being less conductive than insulators with increasing temperatures. | ||
d. band gap size, with insulator band gaps being greater in energy than those of semiconductors. |
a. intrinsic semiconductor. | ||
b. high-temperature superconductor. | ||
c. low-temperature superconductor. | ||
d. extrinsic semiconductor. |
a. I | ||
b. II | ||
c. I and II | ||
d. none of the above |
a. 2 | ||
b. 6 | ||
c. 8 | ||
d. 14 |
a. I | ||
b. II | ||
c. I and II | ||
d. none of the above |
a. intrinsic semiconductors. | ||
b. high-temperature superconductors. | ||
c. low-temperature superconductors. | ||
d. extrinsic semiconductors. |
a. I- | ||
b. Br- | ||
c. Cl- | ||
d. F- |
a. 0 | ||
b. 2 | ||
c. 5 | ||
d. 7 |
a. The Lewis acid becomes softer. | ||
b. The Lewis acid becomes harder. | ||
c. No change is observed. | ||
d. The Lewis acid behaves as a base. |
a. 2.27 x 10-12 | ||
b. 1.48 x 10-10 | ||
c. 6.76 x 10-5 | ||
d. 4.66 x 10-2 |
a. No change is observed. | ||
b. The Lewis base becomes harder. | ||
c. The Lewis base becomes softer. | ||
d. The Lewis base behaves as an acid. |
a. HI | ||
b. HF | ||
c. HCl | ||
d. HBr |
a. C-O | ||
b. C-C | ||
c. C-S | ||
d. C-N |
a. NH3 | ||
b. HgCl2 | ||
c. Hg(NH3)2 | ||
d. Cl- |
a. acid. | ||
b. base. | ||
c. chelator | ||
d. catalyst. |
a. acid. | ||
b. base. | ||
c. both A and B | ||
d. none of the above |
a. FeSO43, 3Ag2SO4, 3Pt(SCN)4 | ||
b. Fe2(SO4)3, 6Ag2SO4, 3Pt(SCN)4 | ||
c. Fe2(SO4)3, 6Ag2SO4, 3Pt(SCN)2 | ||
d. Fe2(SO4)3, 3Ag2SO4, 3Pt(SCN)4 |
a. Ag+ | ||
b. Ru3+ | ||
c. Be2+ | ||
d. Zn2+ |
a. Pt4+ | ||
b. Cd2+ | ||
c. Ni2+ | ||
d. Fe3+ |
a. HI | ||
b. HF | ||
c. HBr | ||
d. HCl |
a. oxalic acid | ||
b. carbon monoxide | ||
c. carbon suboxide | ||
d. carbon dioxide |
a. RbNO3 | ||
b. LiNO3 | ||
c. NaNO3 | ||
d. KNO3 |
a. aluminum | ||
b. boron | ||
c. indium | ||
d. gallium |
a. PbO | ||
b. SiO | ||
c. CO | ||
d. GeO |
a. Phosphorus has an additional electron shell. | ||
b. Phosphorus has two more valence electrons than nitrogen. | ||
c. Phosphorus is more electronegative than nitrogen. | ||
d. Nitrogen has three unpaired electrons in its ground state. |
a. oxygen | ||
b. sulfur | ||
c. selenium | ||
d. tellurium |
a. HClO. | ||
b. HClO2. | ||
c. HClO3. | ||
d. HClO4. |
a. bromine | ||
b. chlorine | ||
c. iodine | ||
d. fluorine |
a. The electronegativity increases with additional electron shells. | ||
b. The electrons of the larger metals are farther from the nucleus and easier to remove. | ||
c. The smaller metals have a greater attraction to the lone pairs on the H2O oxygens. | ||
d. The presence of d-orbital electrons in the larger metals allows for decreased water reactivity. |
a. 2+ | ||
b. 3+ | ||
c. 3- | ||
d. 5+ |
a. calcium | ||
b. rubidium | ||
c. indium | ||
d. silicon |
a. Group 2 | ||
b. Group 3 | ||
c. Group 4 | ||
d. Group 5 |
a. strontium | ||
b. potassium | ||
c. magnesium | ||
d. gallium |
a. Group 1 | ||
b. Group 2 | ||
c. Group 5 | ||
d. Group 7 |