Chapter 14: Problem 19
Anions containing hydrogen (for example, \(\mathrm{HCO}_{3}^{-}\) and \(\left.\mathrm{H}_{2} \mathrm{PO}_{4}^{-}\right)\) usually show amphoteric behavior. Write equations illustrating the amphoterism of these two anions.
Chapter 14: Problem 19
Anions containing hydrogen (for example, \(\mathrm{HCO}_{3}^{-}\) and \(\left.\mathrm{H}_{2} \mathrm{PO}_{4}^{-}\right)\) usually show amphoteric behavior. Write equations illustrating the amphoterism of these two anions.
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Get started for freeArsenic acid \(\left(\mathrm{H}_{3} \mathrm{AsO}_{4}\right)\) is a triprotic acid with \(K_{\mathrm{a}_{1}}=5.5 \times\) \(10^{-3}, K_{\mathrm{a}_{2}}=1.7 \times 10^{-7}\), and \(K_{\mathrm{a}_{3}}=5.1 \times 10^{-12}\). Calculate \(\left[\mathrm{H}^{+}\right],\left[\mathrm{OH}^{-}\right],\left[\mathrm{H}_{3} \mathrm{AsO}_{4}\right],\left[\mathrm{H}_{2} \mathrm{AsO}_{4}^{-}\right],\left[\mathrm{HAsO}_{4}^{2-}\right]\), and \(\left[\mathrm{AsO}_{4}{ }^{3-}\right]\) in a \(0.20-M\) arsenic acid solution.
Quinine \(\left(\mathrm{C}_{20} \mathrm{H}_{24} \mathrm{~N}_{2} \mathrm{O}_{2}\right)\) is the most important alkaloid derived from cinchona bark. It is used as an antimalarial drug. For quinine, \(\mathrm{p} K_{\mathrm{b}_{\mathrm{b}}}=5.1\) and \(\mathrm{p} K_{\mathrm{b}_{2}}=9.7\left(\mathrm{p} K_{\mathrm{b}}=-\log K_{\mathrm{b}}\right) .\) Only \(1 \mathrm{~g}\) quinine will dissolve in \(1900.0 \mathrm{~mL}\) of solution. Calculate the \(\mathrm{pH}\) of a saturated aqueous solution of quinine. Consider only the reaction \(\mathrm{Q}+\mathrm{H}_{2} \mathrm{O} \rightleftharpoons \mathrm{QH}^{+}+\mathrm{OH}^{-}\) described by \(\mathrm{p} K_{\mathrm{b}_{1}}\), where \(\mathrm{Q}=\) quinine.
Codeine \(\left(\mathrm{C}_{18} \mathrm{H}_{21} \mathrm{NO}_{3}\right)\) is a derivative of morphine that is used as an analgesic, narcotic, or antitussive. It was once commonly used in cough syrups but is now available only by prescription because of its addictive properties. If the \(\mathrm{pH}\) of a \(1.7 \times 10^{-3}-M\) solution of codeine is \(9.59\), calculate \(K_{\mathrm{b}}\).
Students are often surprised to learn that organic acids, such as acetic acid, contain - OH groups. Actually, all oxyacids contain hydroxyl groups. Sulfuric acid, usually written as \(\mathrm{H}_{2} \mathrm{SO}_{4}\), has the structural formula \(\mathrm{SO}_{2}(\mathrm{OH})_{2}\), where \(\mathrm{S}\) is the central atom. Identify the acids whose structural formulas are shown below. Why do they behave as acids, while \(\mathrm{NaOH}\) and \(\mathrm{KOH}\) are bases? a. \(\mathrm{SO}(\mathrm{OH})_{2}\) b. \(\mathrm{ClO}_{2}(\mathrm{OH})\) c. \(\mathrm{HPO}(\mathrm{OH})_{2}\)
For solutions of the same concentration, as acid strength increases, indicate what happens to each of the following (increases, decreases, or doesn't change). a. \(\left[\mathrm{H}^{+}\right]\) d. \(\mathrm{pOH}\) b. \(\mathrm{pH}\) e. \(K_{\mathrm{a}}\) c. \(\left[\mathrm{OH}^{-}\right]\)
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