Chapter 21: Problem 82
Explain the important distinction between each pair of terms: (a) peroxide and superoxide; (b) quicklime and slaked lime; (c) soap and detergent; (d) silicate and silicone; (e) sol and gel.
Chapter 21: Problem 82
Explain the important distinction between each pair of terms: (a) peroxide and superoxide; (b) quicklime and slaked lime; (c) soap and detergent; (d) silicate and silicone; (e) sol and gel.
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Get started for freeA chemical that should exist as a crystalline solid is seen to be a mixture of a solid and liquid in a container on a storeroom shelf. Give a plausible reason for that observation. Should the chemical be discarded or is it still useful for some purposes?
A temporary fix for a "sticky" lock is to scrape a pencil point across the notches on the key and to work the key in and out of the lock a few times. What is the basis of this fix?
Write Lewis structures for the following species, both of which involve coordinate covalent bonding: (a) tetrafluoroborate ion, \(\mathrm{BF}_{4}^{-}\), used in metal cleaning and in electroplating baths (b) boron trifluoride ethylamine, used in curing epoxy resins (ethylamine is \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{NH}_{2}\) )
Lithium superoxide, \(\mathrm{LiO}_{2}(\mathrm{s}),\) has never been isolated. Use ideas from Chapter \(12,\) together with data from this chapter and Appendix \(D\), to estimate \(\Delta H_{f}\) for \(\mathrm{LiO}_{2}(\mathrm{s})\) and assess whether \(\mathrm{LiO}_{2}(\mathrm{s})\) is thermodynamically stable with respect to \(\mathrm{Li}_{2} \mathrm{O}(\mathrm{s})\) and \(\mathrm{O}_{2}(\mathrm{g}).\) (a) Use the Kapustinskii equation, along with appropriate data below, to estimate the lattice energy, \(U,\) for \(\left.\mathrm{LiO}_{2}(\mathrm{s}) . \text { (See exercise } 126 \text { in Chapter } 12 .\right)\) The ionic radii for \(L\) i \(^{+}\) and \(O_{2}^{-}\) are \(73 \mathrm{pm}\) and \(144 \mathrm{pm},\) respectively. (b) Use your result from part (a) in the BornFajans-Haber cycle to estimate \(\Delta H_{\mathrm{f}}^{2}\) for \(\mathrm{LiO}_{2}(\mathrm{s})\) [Hint: For the process \(\mathrm{O}_{2}(\mathrm{g})+\mathrm{e}^{-} \rightarrow \mathrm{O}_{2}^{-}(\mathrm{g}), \Delta H^{\circ}=.\) \(-43 \mathrm{kJ} \mathrm{mol}^{-1} .\) See Table 21.2 and Appendix \(\mathrm{D}\) for the other data that are required.] (c) Use your result from part (b) to calculate the enthalpy change for the decomposition of \(\mathrm{LiO}_{2}(\mathrm{s})\) to \(\mathrm{Li}_{2} \mathrm{O}(\mathrm{s})\) and \(\mathrm{O}_{2}(\mathrm{g}) .\) For \(\mathrm{Li}_{2} \mathrm{O}(\mathrm{s}), \Delta H_{\mathrm{f}}^{\circ}=-598.73\) \(\mathrm{kJmol}^{-1}.\) (d) Use your result from part (c) to decide whether \(\mathrm{LiO}_{2}(\mathrm{s})\) is thermodynamically stable with respect to \(\mathrm{Li}_{2} \mathrm{O}(\mathrm{s})\) and \(\mathrm{O}_{2}(\mathrm{g}) .\) Assume that entropy effects can be neglected.
The chemical equation for the hydration of an alkali metal ion is \(M^{+}(g) \rightarrow M^{+}(a q) .\) The Gibbs energy change and the enthalpy change for the process are denoted by \(\Delta G_{\text {hydr. }}^{\circ}\) and \(\Delta H_{\text {hydr. }}^{\circ}\) respectively. \(\Delta G_{\text {hydr. }}^{\circ}\) and \(\Delta H_{\text {hydr. values are given below for the alkali }}\) metal ions. $$\mathrm{M}^{+} \quad \mathrm{Li}^{+} \quad \mathrm{Na}^{+} \quad \mathrm{K}^{+} \quad \mathrm{Rb}^{+} \quad \mathrm{Cs}^{+}$$ $$\begin{array}{llllll} \Delta H_{\text {hydr. }}^{\circ} & -522 & -407 & -324 & -299 & -274 \mathrm{kJ} \mathrm{mol}^{-1} \end{array}$$ $$\begin{array}{llllll} \Delta G_{\text {hydr. }}^{\circ} & -481 & -375 & -304 & -281 & -258 \mathrm{kJ} \mathrm{mol}^{-1} \end{array}$$ Use the data above to calculate \(\Delta S_{\text {hydr. }}^{\circ}\) values for the hydration process. Explain the trend in the \(\Delta S_{\text {hydr. }}^{\circ}\) values.
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