|
1 | | What is the proper Lewis structure of HNO3? |
| | A) | (3.0K) |
| | B) | (13.0K) |
| | C) | (11.0K) |
| | D) | (14.0K) |
|
|
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 |
|
|
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 |
|
|
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. |
|
|
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 |
|
|
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 |
|
|
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 |
|
|
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 |
|
|
9 | | How many resonance structures can be drawn for the following molecule? (12.0K) |
| | A) | 1 |
| | B) | 4 |
| | C) | 3 |
| | D) | 2 |
|
|
10 | | How many other major contributing resonance structures are possible for the following heterocycle?
(12.0K) |
| | A) | 2 |
| | B) | 4 |
| | C) | 6 |
| | D) | 8 |
|
|
11 | | How many energetically equivalent resonance structures exist for the oxalate dianion? (11.0K) |
| | A) | 1 |
| | B) | 2 |
| | C) | 3 |
| | D) | 4 |
|
|
12 | | What is the electron configuration for oxygen? |
| | A) | 1s2 2s2 2p6 |
| | B) | 1s2 2s2 2p5 |
| | C) | 1s2 2s2 2p4 |
| | D) | 1s2 2s2 2p3 |
|
|
13 | | Which of the following compounds does NOT have an octet around the central atom? |
| | A) | NH3 |
| | B) | BH3 |
| | C) | H3O+ |
| | D) | NH4+ |
|
|
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. |
|
|
15 | | A p orbital has what shape? |
| | A) | an oval |
| | B) | a sphere |
| | C) | a wedge of pie |
| | D) | a dumbbell |
|
|
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°. |
|
|
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 |
|
|
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 |
|
|
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 |
|
|
20 | | The geometric shape of acetone, (CH3)2CO, is best described as |
| | A) | linear. |
| | B) | trigonal planar. |
| | C) | bent. |
| | D) | tetrahedral. |
|
|
21 | | The correct geometry around oxygen in CH3OCH3 is |
| | A) | linear. |
| | B) | bent. |
| | C) | tetrahedral. |
| | D) | trigonal planar |
|
|
22 | | Which molecule has the largest dipole moment? |
| | A) | HCl |
| | B) | CCl4 |
| | C) | H2S |
| | D) | CO2 |
|
|
23 | | Which molecule has the smallest dipole moment? |
| | A) | CO2 |
| | B) | CHCl3 |
| | C) | H2O |
| | D) | NH3 |
|
|
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. |
|
|
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) |
|
|
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–. |
|
|
27 | | For the protonation of acetone, the correct curved arrow mechanism is |
| | A) | (13.0K) |
| | B) | (12.0K) |
| | C) | (12.0K) |
| | D) | (13.0K) |
|