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1 |  |  What is the proper Lewis structure of HNO3? |
|  | A) |  (3.0K) |
|  | B) |  (13.0K) |
|  | C) |  (11.0K) |
|  | D) |  (14.0K) |
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2 |  |  How many lone pairs of electrons will be present in the following molecule? CH3–N=N=N |
|  | A) | 0 |
|  | B) | 1 |
|  | C) | 2 |
|  | D) | 3 |
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3 |  |  In the nitrate ion (NO3-), what is the charge on nitrogen? All electrons are shown.
 (15.0K) |
|  | A) | No charge |
|  | B) | - 1 |
|  | C) | + 1 |
|  | D) | + 2 |
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4 |  |  The best Lewis structure for ethyne (C2H2; commonly called “acetylene”) has |
|  | A) | 2 single bonds, 1 triple bond, and 1 lone pair. |
|  | B) | 2 double bonds and 2 lone pairs. |
|  | C) | 2 single bonds, 1 triple bond, and no lone pairs. |
|  | D) | 2 single bonds, 1 double bond, and 2 lone pairs. |
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5 |  |  What is the formal charge (FC) of each atom in the following molecule? NH4+ |
|  | A) | FC Hydrogens: 0
FC Nitrogen: 0 |
|  | B) | FC Hydrogens: 0
FC Nitrogen: -1 |
|  | C) | FC Hydrogens: 0
FC Nitrogen: +2 |
|  | D) | FC Hydrogens: 0
FC Nitrogen: +1 |
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6 |  |  What is the formal charge (FC) of each atom in the following molecule?
BH4- |
|  | A) | FC Boron: 0
FC Hydrogen1: 0
FC Hydrogen2: 0
FC Hydrogen3: 0
FC Hydrogen4: 0 |
|  | B) | FC Boron: 0
FC Hydrogen1: +1
FC Hydrogen2: -1
FC Hydrogen3: 0
FC Hydrogen4: 0 |
|  | C) | FC Boron: -2
FC Hydrogen1: 0
FC Hydrogen2: 0
FC Hydrogen3: 0
FC Hydrogen4: 0 |
|  | D) | FC Boron: -1
FC Hydrogen1: 0
FC Hydrogen2: 0
FC Hydrogen3: 0
FC Hydrogen4: 0 |
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7 |  |  What is the formal charge (FC) of each atom in the following molecule?
 (13.0K) |
|  | A) | FC Carbon: +1
FC Hydrogen1: 0
FC Hydrogen2: 0
FC Hydrogen3: 0 |
|  | B) | FC Carbon: 0
FC Hydrogen1: 0
FC Hydrogen2: 0
FC Hydrogen3: 0 |
|  | C) | FC Carbon: -2
FC Hydrogen1: 0
FC Hydrogen2: 0
FC Hydrogen3: 0 |
|  | D) | FC Carbon: -1
FC Hydrogen1: 0
FC Hydrogen2: 0
FC Hydrogen3: 0 |
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8 |  |  How many total resonance structures can be drawn for the following anion (include those without separation of charge)?
 (15.0K) |
|  | A) | 1 |
|  | B) | 2 |
|  | C) | 3 |
|  | D) | 4 |
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9 |  |  How many resonance structures can be drawn for the following molecule?
 (12.0K) |
|  | A) | 1 |
|  | B) | 4 |
|  | C) | 3 |
|  | D) | 2 |
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10 |  |  How many other major contributing resonance structures are possible for the following heterocycle?
 (12.0K) |
|  | A) | 2 |
|  | B) | 4 |
|  | C) | 6 |
|  | D) | 8 |
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11 |  |  How many energetically equivalent resonance structures exist for the oxalate dianion?
 (11.0K) |
|  | A) | 1 |
|  | B) | 2 |
|  | C) | 3 |
|  | D) | 4 |
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12 |  |  What is the electron configuration for oxygen? |
|  | A) | 1s2 2s2 2p6 |
|  | B) | 1s2 2s2 2p5 |
|  | C) | 1s2 2s2 2p4 |
|  | D) | 1s2 2s2 2p3 |
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13 |  |  Which of the following compounds does NOT have an octet around the central atom? |
|  | A) | NH3 |
|  | B) | BH3 |
|  | C) | H3O+ |
|  | D) | NH4+ |
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14 |  |  Which of the following statements about an sp hybridized carbon is FALSE? |
|  | A) | It is divalent. |
|  | B) | It forms bonds that are linear. |
|  | C) | It has two p orbitals. |
|  | D) | It always forms triple bonds to carbon. |
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15 |  |  A p orbital has what shape? |
|  | A) | an oval |
|  | B) | a sphere |
|  | C) | a wedge of pie |
|  | D) | a dumbbell |
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16 |  |  The hybridization of the central carbon in  (10.0K) and the bond angle CCN are |
|  | A) | sp2, 180°. |
|  | B) | sp, 180°. |
|  | C) | sp2, 120°. |
|  | D) | sp3, 109°. |
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17 |  |  What are the hybridizations of carbons 1 and 2 respectively in the following structure?
 (11.0K) |
|  | A) | sp3 and sp2 |
|  | B) | sp2 and sp3 |
|  | C) | sp3 and sp |
|  | D) | sp2 and sp2 |
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18 |  |  What are the hybridizations of atoms 1 and 2 respectively in the following structure?
 (12.0K) |
|  | A) | sp3 and sp2 |
|  | B) | sp2 and sp3 |
|  | C) | sp3 and sp |
|  | D) | sp2 and sp2 |
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19 |  |  Identify the orbital hybridization at the two indicated carbons in the molecule below.
 (11.0K) |
|  | A) | C1: sp; C2: sp |
|  | B) | C1: sp2; C2: sp2 |
|  | C) | C1: sp; C2: sp2 |
|  | D) | C1: sp2; C2: sp |
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20 |  |  The geometric shape of acetone, (CH3)2CO, is best described as |
|  | A) | linear. |
|  | B) | trigonal planar. |
|  | C) | bent. |
|  | D) | tetrahedral. |
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21 |  |  The correct geometry around oxygen in CH3OCH3 is |
|  | A) | linear. |
|  | B) | bent. |
|  | C) | tetrahedral. |
|  | D) | trigonal planar |
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22 |  |  Which molecule has the largest dipole moment? |
|  | A) | HCl |
|  | B) | CCl4 |
|  | C) | H2S |
|  | D) | CO2 |
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23 |  |  Which molecule has the smallest dipole moment? |
|  | A) | CO2 |
|  | B) | CHCl3 |
|  | C) | H2O |
|  | D) | NH3 |
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24 |  |  Consider the structure with the electron-pushing arrow:
 (10.0K)
Which of the following statements is FALSE? |
|  | A) | The bond between the tertiary carbon and bromine is breaking. |
|  | B) | The products will be a carbon cation and bromine anion. |
|  | C) | This process is called homolytic cleavage. |
|  | D) | The C–Br bonding electrons become a lone pair on the bromine. |
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25 |  |  What is the product of the curved arrow mechanism shown below?
 (14.0K) |
|  | A) |  (14.0K) |
|  | B) | No reaction. |
|  | C) |  (14.0K) |
|  | D) |  (14.0K) |
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26 |  |  In this reaction, HNO3 + H2SO4 → HSO4– + H2NO3+ a curved arrow should point |
|  | A) | from HNO3 to H2SO4. |
|  | B) | from H2SO4 to HNO3. |
|  | C) | from HSO4– to H2NO3+. |
|  | D) | from H2NO3+ to HSO4–. |
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27 |  |  For the protonation of acetone, the correct curved arrow mechanism is |
|  | A) |  (13.0K) |
|  | B) |  (12.0K) |
|  | C) |  (12.0K) |
|  | D) |  (13.0K) |
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