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1 |  |  In the following equilibrium where HX is a stronger acid than HY, predict the position of the equilibrium. NaY + HX  (8.0K) NaX + HY |
|  | A) | The equilibrium favors the weakest acid and the strongest base. |
|  | B) | The equilibrium favors the weakest acid and the weakest base. |
|  | C) | The equilibrium favors the strongest acid and the strongest base. |
|  | D) | The equilibrium favors the strongest acid and the weakest base. |
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2 |  |  In the following equilibrium where HX is a stronger acid than HY. Predict the value of the equilibrium constant K for the reaction. NaX + HY  (8.0K) NaY + HX |
|  | A) | K > 1 |
|  | B) | K < 1 |
|  | C) | K = 0 |
|  | D) | K = 10 |
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3 |  |  What is the product of the following reaction?
 (11.0K) |
|  | A) |  (13.0K) |
|  | B) |  (11.0K) |
|  | C) |  (10.0K) |
|  | D) |  (11.0K) |
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4 |  |  Which of the following compounds can behave as an ACID as well as a BASE? |
|  | A) |  (11.0K) |
|  | B) |  (11.0K) |
|  | C) |  (10.0K) |
|  | D) |  (10.0K) |
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5 |  |  Which molecule or ion plays the role of acid in the following reaction?
HNO3 + H2SO4 → HSO4– + H2NO3+ |
|  | A) | HNO3 |
|  | B) | H2SO4 |
|  | C) | HSO4– |
|  | D) | H2NO3+ |
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6 |  |  What are the product(s) of the following acid–base reaction?
 (11.0K) |
|  | A) |  (12.0K) |
|  | B) |  (12.0K) |
|  | C) |  (12.0K) |
|  | D) |  (12.0K) |
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7 |  |  Using pKa values from the table, which is the strongest acid (HA is any acid).
| pKa | HA | | 3.7 | HCOOH | | 4.2 | C6H5COOH | | 4.75 | CH3COOH | | 15.5 | CH3OH |
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|  | A) | Acetic acid |
|  | B) | Benzoic acid |
|  | C) | Methanol |
|  | D) | Formic acid |
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8 |  |  Which is the strongest base? Use the table.
| pKa | HA | | 15.7 | H2O | | 50 | CH4 | | 18 | (CH3)3COH | | 35 | NH3 |
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|  | A) | Sodium hydroxide |
|  | B) | Methyllithium |
|  | C) | Sodium amide |
|  | D) | Potassium tert-butoxide |
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9 |  |  Which of the following acids has the lower pKa value? |
|  | A) |  (12.0K) |
|  | B) |  (12.0K) |
|  | C) |  (13.0K) |
|  | D) |  (13.0K) |
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10 |  |  The approximate pKa values for the protonated forms of the below compounds are shown. Arrange them in the order of increasing basicity (that is, least basic first and most basic last).
 (11.0K) |
|  | A) | c e b a d |
|  | B) | c b e d a |
|  | C) | c d e a b |
|  | D) | a d e b c |
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11 |  |  Acetic acid, CH3COOH, is |
|  | A) | stronger than HCl. |
|  | B) | weaker than HCl. |
|  | C) | has 4 acidic protons. |
|  | D) | is comparable in strength to HCl. |
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12 |  |  Which of the following statements is NOT correct concerning pKa’s and acidity and basicity? |
|  | A) | A higher pKa value means the acid is less acidic. |
|  | B) | A lower pKa value for the acid means the conjugate base is more basic. |
|  | C) | In an acid–base reaction, the equilibrium lies on the side of the acid with the higher pKa. |
|  | D) | An acid–base reaction will proceed in the direction toward the weaker base. |
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13 |  |  The pKa of phenol is 10. Which of the following bases will deprotonate phenol completely?
NaNH2 (pKa of NH3 = 35)
NaOH (pKa of H2O = 16)
NH3 (pKa of NH4+ = 10)
NaOCOCH3 (pKa of HOCOCH3 = 5) |
|  | A) | NaNH2 only |
|  | B) | NH3 only |
|  | C) | NaNH2 and NaOH |
|  | D) | NH3 and NaOCOCH3 |
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14 |  |  Predict the favorable direction of the two acid–base equilibria shown below.
 (17.0K) |
|  | A) | Equilibrium A: right; equilibrium B: right. |
|  | B) | Equilibrium A: left; equilibrium B: left. |
|  | C) | Equilibrium A: right; equilibrium B: left. |
|  | D) | Equilibrium A: left; equilibrium B: right. |
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15 |  |  Which compound has the least acidic hydrogen? |
|  | A) | acetylene |
|  | B) | ethylene |
|  | C) | ethane |
|  | D) | allene |
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16 |  |  Which is the weakest base? |
|  | A) | –CH3 |
|  | B) | –F |
|  | C) | –NH2 |
|  | D) | –OH |
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17 |  |  Rank the following compounds in order from most basic to least basic.
 (18.0K) |
|  | A) | 2 > 3 > 4 > 1 |
|  | B) | 4 > 3 > 1 > 2 |
|  | C) | 3 > 1 > 2 > 4 |
|  | D) | 1 > 4 > 3 > 2 |
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18 |  |  Rank the following compounds in order from most acidic to least acidic.
 (4.0K) |
|  | A) | c > d > a > b |
|  | B) | d> a > b > c |
|  | C) | b > a > d > c |
|  | D) | a > b > d > c |
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19 |  |  Which is the weakest acid? |
|  | A) | ethane, C2H6 |
|  | B) | ethyne, C2H2 |
|  | C) | ethanol, C2H5OH |
|  | D) | ethylene, C2H4 |
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20 |  |  Which is the strongest base? |
|  | A) | NH3 |
|  | B) | BH3 |
|  | C) | PH3 |
|  | D) | H2O |
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21 |  |  Which is the strongest base? |
|  | A) | LiOH |
|  | B) | CH3Li |
|  | C) | LiNH2 |
|  | D) | LiF |
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22 |  |  Which is the strongest Lewis acid? |
|  | A) | BF3 |
|  | B) | BH3 |
|  | C) | BCl3 |
|  | D) | BBr3 |
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23 |  |  Rank the following acids in order from most acidic to least acidic.
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|  | A) | HCl> H2O > CH3COOH > NH3 |
|  | B) | CH3COOH >HCl > H2O > NH3 |
|  | C) | HCl > CH3COOH > H2O > NH3 |
|  | D) | H2O > NH3> HCl > CH3COOH |
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24 |  |  Rank the following bases in order from most basic to least basic.
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|  | A) | CH3Li > LiOH > LiNH2> LiF |
|  | B) | LiOH > CH3Li > LiF > LiNH2 |
|  | C) | CH3Li > LiNH2> LiOH > LiF |
|  | D) | LiNH2> LiOH > LiF > CH3Li |
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25 |  |  NaNH2 can deprotonate HC≡CH but not CH2=CH2. Use this observation and the hybridization effect to order the following four acids from most acidic to least acidic.
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|  | A) | NH3 > CH3–CH3> CH2=CH2 > HC≡CH |
|  | B) | CH3–CH3> CH2=CH2 > NH3 > HC≡CH |
|  | C) | HC≡CH > NH3 > CH2=CH2 > CH3–CH3 |
|  | D) | CH3–CH3 > NH3 > CH2=CH2 > HC≡CH |
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