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Predict the products of the following acid-base reactions, and predict whether the equilibrium lies to the left or to the right of the equation: (a) \(\mathrm{O}^{2-}(a q)+\mathrm{H}_{2} \mathrm{O}(l) \rightleftharpoons\) (b) \(\mathrm{CH}_{3} \mathrm{COOH}(a q)+\mathrm{HS}^{-}(a q) \rightleftharpoons\) (c) \(\mathrm{NO}_{2}^{-}(a q)+\mathrm{H}_{2} \mathrm{O}(l) \rightleftharpoons\)

Short Answer

Expert verified
\(a)\): The products are \(OH^-(aq)\) and \(OH^-(aq)\), and the equilibrium lies to the left. \(b)\): The products are \(CH_3COO^-(aq)\) and \(H_2S(aq)\), and the equilibrium lies slightly to the right. \(c)\): The products are \(OH^-(aq)\) and \(HNO_2(aq)\), and the equilibrium lies to the left.

Step by step solution

01

a) Identifying Acid and Base in the equation

In this reaction, we have \(\mathrm{O^{2-}}(a q)\) reacting with \(\mathrm{H_2O}(l)\). \(\mathrm{O^{2-}}\) is a base, as it can accept protons, while \(\mathrm{H_2O}\) acts as an acid.
02

b) Predicting the products

Based on the given reactants, the products will be formed upon the transfer of a proton from \(\mathrm{H_2O}\) to \(\mathrm{O^{2-}}\). Therefore, the products will be: \(OH^-(aq) + OH^-(aq)\)
03

c) Determining the equilibrium direction

In this case, the equilibrium constant for this reaction can be represented as: \(K=\frac{[\mathrm{OH^-}][\mathrm{OH^-}]}{[\mathrm{O^{2-}}][\mathrm{H_2O}]}\) Since \(\mathrm{O^{2-}}\) is a weak base, and \(\mathrm{H_2O}\) is a weak acid, the equilibrium will lie to the left, favoring the formation of reactants.
04

a) Identifying Acid and Base in the equation

In this reaction, we have \(\mathrm{CH_3COOH} (a q)\) reacting with \(\mathrm{HS^-(a q)}\). \(\mathrm{CH_3COOH}\) is an acid, while \(\mathrm{HS^-}\) is a base.
05

b) Predicting the products

The products will be formed upon the transfer of a proton from \(\mathrm{CH_3COOH}\) to \(\mathrm{HS^-}\). Therefore, the products will be: \(CH_3COO^-(aq) + H_2S(aq)\)
06

c) Determining the equilibrium direction

In this case, the equilibrium constant for this reaction can be represented as: \(K=\frac{[\mathrm{CH_3COO^-}][\mathrm{H_2S}]}{[\mathrm{CH_3COOH}][\mathrm{HS^-}]}\) Since \(\mathrm{CH_3COOH}\) is a weak acid and \(\mathrm{HS^-}\) is a weak base, the equilibrium direction depends on their relative strengths. In this case, the equilibrium will lie slightly to the right, favoring the formation of products.
07

a) Identifying Acid and Base in the equation

In this reaction, we have \(\mathrm{NO_2^{-}}(a q)\) reacting with \(\mathrm{H_2O}(l)\). \(\mathrm{NO_2^{-}}\) acts as a base, while \(\mathrm{H_2O}\) will be an acid.
08

b) Predicting the products

The products will be formed upon the transfer of a proton from \(\mathrm{H_2O}\) to \(\mathrm{NO_2^{-}}\). Therefore, the products will be: \(OH^-(aq) + HNO_2(aq)\)
09

c) Determining the equilibrium direction

In this case, the equilibrium constant for this reaction can be represented as: \(K=\frac{[\mathrm{OH^-}][\mathrm{HNO_2}]}{[\mathrm{NO_2^-}][\mathrm{H_2O}]}\) \(\mathrm{NO_2^-}\) is a weak base, and \(\mathrm{H_2O}\) is a weak acid, so the equilibrium will lie to the left, favoring the formation of reactants.

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Most popular questions from this chapter

Predict whether the equilibrium lies to the right or to the left in the following reactions: (a) \(\mathrm{NH}_{4}^{+}(a q)+\mathrm{PO}_{4}{ }^{3-}(a q) \rightleftharpoons\) \(\mathrm{NH}_{3}(a q)+\mathrm{HPO}_{4}^{2-}(a q)\) (The ammonium ion is a stronger acid than the hydrogen phosphate ion.) (b) \(\mathrm{CH}_{3} \mathrm{COOH}(a q)+\mathrm{CN}^{-}(a q) \rightleftharpoons\) \(\mathrm{CH}_{3} \mathrm{COO}^{-}(a q)+\mathrm{HCN}(a q)\) (The cyanide ion is a stronger base than the acetate ion.)

Calculate \(\left[\mathrm{H}^{+}\right]\) for each of the following solutions, and indicate whether the solution is acidic, basic, or neutral: (a) \(\left[\mathrm{OH}^{-}\right]=0.00045 \mathrm{M}\); (b) \(\left[\mathrm{OH}^{-}\right]=8.8 \times 10^{-9} \mathrm{M} ;(\mathrm{c})\) solution in which \(\left[\mathrm{OH}^{-}\right]\) is 100 times greater than \(\left[\mathrm{H}^{+}\right]\).

Calculate \(\left[\mathrm{OH}^{-}\right]\) and \(\mathrm{pH}\) for (a) \(1.5 \times 10^{-3} \mathrm{M} \mathrm{Sr}(\mathrm{OH})_{2}\) (b) \(2.250 \mathrm{~g}\) of \(\mathrm{LiOH}\) in \(250.0 \mathrm{~mL}\) of solution, \((c) 100 \mathrm{~mL}\) of \(0.175 \mathrm{M} \mathrm{NaOH}\) diluted to \(2.00 \mathrm{~L},(\mathrm{~d})\) a solution formed by adding \(5.00 \mathrm{~mL}\) of \(0.105 \mathrm{M} \mathrm{KOH}\) to \(15.0 \mathrm{~mL}\) of \(9.5 \times 10^{-2} \mathrm{M} \mathrm{Ca}(\mathrm{OH})_{2}\)

The acid-dissociation constant for hypochlorous acid (HClO) is \(3.0 \times 10^{-8}\). Calculate the concentrations of \(\mathrm{H}_{3} \mathrm{O}^{+}, \mathrm{ClO}^{-}\), and \(\mathrm{HClO}\) at equilibrium if the initial concentration of \(\mathrm{HClO}\) is \(0.0090 \mathrm{M}\).

Many moderately large organic molecules containing basic nitrogen atoms are not very soluble in water as neutral molecules, but they are frequently much more soluble as their acid salts. Assuming that \(\mathrm{pH}\) in the stomach is \(2.5\), indicate whether each of the following compounds would be present in the stomach as the neutral base or in the protonated form: nicotine, \(K_{b}=7 \times 10^{-7} ;\) caffeine, \(K_{b}=4 \times 10^{-14} ;\) strychnine, \(K_{b}=1 \times 10^{-6} ;\) quinine, \(K_{b}=1.1 \times 10^{-6}\)

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