SMARTWORKS FOR CHEMISTRY: ATOMS FOCUSED
2nd Edition
ISBN: 9780393644777
Author: Gilbert
Publisher: MCGRAW-HILL HIGHER EDUCATION
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SMARTWORKS FOR CHEMISTRY: ATOMS FOCUSED
Ch. 16 - Prob. 16.1VPCh. 16 - Prob. 16.2VPCh. 16 - Prob. 16.3VPCh. 16 - Prob. 16.4VPCh. 16 - Prob. 16.5VPCh. 16 - Prob. 16.6VPCh. 16 - Prob. 16.7VPCh. 16 - Prob. 16.8VPCh. 16 - Prob. 16.9VPCh. 16 - Prob. 16.10VP
Ch. 16 - Prob. 16.11QACh. 16 - Prob. 16.12QACh. 16 - Prob. 16.13QACh. 16 - Prob. 16.14QACh. 16 - Prob. 16.15QACh. 16 - Prob. 16.16QACh. 16 - Prob. 16.17QACh. 16 - Prob. 16.18QACh. 16 - Prob. 16.19QACh. 16 - Prob. 16.20QACh. 16 - Prob. 16.21QACh. 16 - Prob. 16.22QACh. 16 - Prob. 16.23QACh. 16 - Prob. 16.24QACh. 16 - Prob. 16.25QACh. 16 - Prob. 16.26QACh. 16 - Prob. 16.27QACh. 16 - Prob. 16.28QACh. 16 - Prob. 16.29QACh. 16 - Prob. 16.30QACh. 16 - Prob. 16.31QACh. 16 - Prob. 16.32QACh. 16 - Prob. 16.33QACh. 16 - Prob. 16.34QACh. 16 - Prob. 16.35QACh. 16 - Prob. 16.36QACh. 16 - Prob. 16.37QACh. 16 - Prob. 16.38QACh. 16 - Prob. 16.39QACh. 16 - Prob. 16.40QACh. 16 - Prob. 16.41QACh. 16 - Prob. 16.42QACh. 16 - Prob. 16.43QACh. 16 - Prob. 16.44QACh. 16 - Prob. 16.45QACh. 16 - Prob. 16.46QACh. 16 - Prob. 16.47QACh. 16 - Prob. 16.48QACh. 16 - Prob. 16.49QACh. 16 - Prob. 16.50QACh. 16 - Prob. 16.51QACh. 16 - Prob. 16.52QACh. 16 - Prob. 16.53QACh. 16 - Prob. 16.54QACh. 16 - Prob. 16.55QACh. 16 - Prob. 16.56QACh. 16 - Prob. 16.57QACh. 16 - Prob. 16.58QACh. 16 - Prob. 16.59QACh. 16 - Prob. 16.60QACh. 16 - Prob. 16.61QACh. 16 - Prob. 16.62QACh. 16 - Prob. 16.63QACh. 16 - Prob. 16.64QACh. 16 - Prob. 16.65QACh. 16 - Prob. 16.66QACh. 16 - Prob. 16.67QACh. 16 - Prob. 16.68QACh. 16 - Prob. 16.69QACh. 16 - Prob. 16.70QACh. 16 - Prob. 16.71QACh. 16 - Prob. 16.72QACh. 16 - Prob. 16.73QACh. 16 - Prob. 16.74QACh. 16 - Prob. 16.75QACh. 16 - Prob. 16.76QACh. 16 - Prob. 16.77QACh. 16 - Prob. 16.78QACh. 16 - Prob. 16.79QACh. 16 - Prob. 16.80QACh. 16 - Prob. 16.81QACh. 16 - Prob. 16.82QACh. 16 - Prob. 16.83QACh. 16 - Prob. 16.84QACh. 16 - Prob. 16.85QACh. 16 - Prob. 16.86QACh. 16 - Prob. 16.87QACh. 16 - Prob. 16.88QACh. 16 - Prob. 16.89QACh. 16 - Prob. 16.90QACh. 16 - Prob. 16.91QACh. 16 - Prob. 16.92QACh. 16 - Prob. 16.93QACh. 16 - Prob. 16.94QACh. 16 - Prob. 16.95QACh. 16 - Prob. 16.96QACh. 16 - Prob. 16.97QACh. 16 - Prob. 16.98QACh. 16 - Prob. 16.99QACh. 16 - Prob. 16.100QACh. 16 - Prob. 16.101QACh. 16 - Prob. 16.102QACh. 16 - Prob. 16.103QACh. 16 - Prob. 16.104QACh. 16 - Prob. 16.105QACh. 16 - Prob. 16.106QACh. 16 - Prob. 16.107QACh. 16 - Prob. 16.108QACh. 16 - Prob. 16.109QACh. 16 - Prob. 16.110QACh. 16 - Prob. 16.111QACh. 16 - Prob. 16.112QACh. 16 - Prob. 16.113QACh. 16 - Prob. 16.114QACh. 16 - Prob. 16.115QACh. 16 - Prob. 16.116QACh. 16 - Prob. 16.117QACh. 16 - Prob. 16.118QACh. 16 - Prob. 16.119QACh. 16 - Prob. 16.120QACh. 16 - Prob. 16.121QACh. 16 - Prob. 16.122QACh. 16 - Prob. 16.123QACh. 16 - Prob. 16.124QACh. 16 - Prob. 16.125QACh. 16 - Prob. 16.126QACh. 16 - Prob. 16.127QACh. 16 - Prob. 16.128QACh. 16 - Prob. 16.129QACh. 16 - Prob. 16.130QACh. 16 - Prob. 16.131QACh. 16 - Prob. 16.132QACh. 16 - Prob. 16.133QACh. 16 - Prob. 16.134QACh. 16 - Prob. 16.135QACh. 16 - Prob. 16.136QA
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- The pH of a 0.10-M solution of propanoic acid, CH3CH2COOH, a weak organic acid, is measured at equilibrium and found to be 2.93 at 25 °C. Calculate the Ka of propanoic acid.arrow_forwardFind the value of Kb for the conjugate base of the following organic acids. (a) picric acid used in the manufacture of explosives; Ka = 0.16 (b) trichloroacetic acid used in the treatment of warts; Ka = 0.20arrow_forwardWhich acid has the strongest conjugate base? (a) HNO2 (b) C6H5CO2H (c) HCN (d) HClarrow_forward
- Lactic acid, C3H6O3, occurs in sour milk as a result of the metabolism of certain bacteria. Calculate the pH of a solution of 56. mg lactic acid in 250. mL water. Ka for D-lactic acid is 1.5 × 10−4.arrow_forwardA solution of acetic acid, HC2H3O2, on a laboratory shelf was of undetermined concentration. If the pH of the solution was found to be 2.57, what was the concentration of the acetic acid? The Ka of acetic acid is 1.7 105.arrow_forwardWrite chemical equations showing the individual proton-transfer steps that occur in aqueous solution for each of the following acids. a. H2CO3 (carbonic acid) b. H2C3H2O4 (malonic acid)arrow_forward
- Write the chemical equation and the expression for the equilibrium constant, and calculate Kb for the reaction of each of the following ions as a base. (a) sulfate ion (b) citrate ionarrow_forwardWrite chemical equations showing the individual proton-transfer steps that occur in aqueous solution for each of the following acids. a. H2C2O4 (oxalic acid) b. H2C4H4O6 (tartaric acid)arrow_forwardA chemist wanted to determine the concentration of a solution of lactic acid, HC3H5O3. She found that the pH of the solution was 2.60. What was the concentration of the solution? The Kd of lactic acid is 1.4 104.arrow_forward
- Consider these acids (a) Arrange the acids in order of increasing acid strength from weakest to strongest. (b) Which acid has the smallest pKa value?arrow_forwardFor conjugate acidbase pairs, how are Ka and Kb related? Consider the reaction of acetic acid in water CH3CO2H(aq)+H2O(l)CH3CO2(aq)+H3O+(aq) where Ka = 1.8 105 a. Which two bases are competing for the proton? b. Which is the stronger base? c. In light of your answer to part b. why do we classify the acetate ion (CH3CO2) as a weak base? Use an appropriate reaction to justify your answer. In general, as base strength increases, conjugate acid strength decreases. Explain why the conjugate acid of the weak base NH3 is a weak acid. To summarize, the conjugate base of a weak acid is a weak base and the conjugate acid of a weak base is a weak acid (weak gives you weak). Assuming Ka for a monoprotic strong acid is 1 106, calculate Kb for the conjugate base of this strong acid. Why do conjugate bases of strong acids have no basic properties in water? List the conjugate bases of the six common strong acids. To tie it all together, some instructors have students think of Li+, K+, Rb+, Cs+, Ca2+, Sr2+, and Ba2+ as the conjugate acids of the strong bases LiOH, KOH. RbOH, CsOH, Ca(OH)2, Sr(OH)2, and Ba(OH)2. Although not technically correct, the conjugate acid strength of these cations is similar to the conjugate base strength of the strong acids. That is, these cations have no acidic properties in water; similarly, the conjugate bases of strong acids have no basic properties (strong gives you worthless). Fill in the blanks with the correct response. The conjugate base of a weak acid is a_____base. The conjugate acid of a weak base is a_____acid. The conjugate base of a strong acid is a_____base. The conjugate acid of a strong base is a_____ acid. (Hint: Weak gives you weak and strong gives you worthless.)arrow_forwardThe active ingredient formed by aspirin in the body is salicylic acid, C6H4OH(CO2H). The carboxyl group. (-CO2H) acts as a weak acid. The phenol group (an OH group bonded to an aromatic ring) also acts as an acid but a much weaker acid. List, in order of descending concentration, all of the ionic and molecular species present in a 0.001-M aqueous solution of C6H4OH(CO2H).arrow_forward
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