Chemistry: An Atoms-Focused Approach (Second Edition)
2nd Edition
ISBN: 9780393614053
Author: Thomas R. Gilbert, Rein V. Kirss, Stacey Lowery Bretz, Natalie Foster
Publisher: W. W. Norton & Company
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Chapter 16 Solutions
Chemistry: An Atoms-Focused Approach (Second Edition)
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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- Write a chemical equation to describe the proton transfer that occurs when each of these acids is added to water. (a) HCO3 (b) HCl (c) CH3COOH (d) HCNarrow_forwardIn each of the following acid-base reactions, identify the Brnsted acid and base on the left and their conjugate partners on the right. (a) C2H5N(aq) + CH3CO2H(aq) C5H5NH+(aq) + CH3CO2(aq) (b) N2H4(aq) + HSO4(aq) N2H5+(aq) + SO42(aq) (c) [Al(H2O)6]3+ (aq) + OH(aq) [Al(H2O)5OH]2+ (aq) + H2O+()arrow_forwardThe 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_forward
- In each of the following acid-base reactions, identify the Brnsted acid and base on the left and their conjugate partners on the right. (a) HCO2H(aq) + H2O() HCO2(aq) + H3O+(aq) (b) NH3(aq) + H2S(aq) NH4+(aq) + HS(aq) (c) HSO4(aq) + OH(aq) SO42(aq) + H2O+()arrow_forwardWrite a chemical equation to describe the proton transfer that occurs when each of these acids is added to water. (a) HIO (b) CH3(CH2)4COOH (c) HOOCCOOH (d) CH3NH3+arrow_forwardWhat is the freezing point of vinegar, which is an aqueous solution of 5.00% acetic acid, HC2H3O2, by mass (d=1.006g/cm3)?arrow_forward
- Using the diagrams shown in Problem 10-37, which of the four acids is the weakest acid?arrow_forwardWrite the chemical equation for the ionization of the following weak acids. Assume only one hydrogen ionizes in all cases. (a) hydrazoic add, HN3 (b) citric acid, H2C6H6O7 (c) squaric acid, H2C4O4arrow_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
- For 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_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 hydrogen atom in the organic base pyridine, C5H5N, can be substituted by various atoms or groups to give XC5H4N, where X is an atom such as Cl or a group such as CH3. The following table gives Ka values for the conjugate acids of a variety of substituted pyridines. (a) Suppose each conjugate acid is dissolved in sufficient water to give a 0.050 M solution. Which solution would have the highest pH? The lowest pH? (b) Which of the substituted pyridines is the strongest Brnsted base? Which is the weakest Brnsted base?arrow_forward
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