Choose the substance with the larger positional probability in each case. a. 1 mole of \(\mathrm{H}_{2}\) (at \(\mathrm{STP} )\) or 1 mole of $\mathrm{H}_{2}\left(\text { at } 100^{\circ} \mathrm{C}, 0.5 \mathrm{atm}\right)$ b. 1 mole of \(\mathrm{N}_{2}(\text { at } \mathrm{STP})\) or 1 mole of \(\mathrm{N}_{2}(\text { at } 100 \mathrm{K}, 2.0 \mathrm{atm})\) c. 1 mole of \(\mathrm{H}_{2} \mathrm{O}(s)\) (at \(0^{\circ} \mathrm{C} )\) or 1 \(\mathrm{mole}\) of $\mathrm{H}_{2} \mathrm{O}(l)\left(\mathrm{at} 20^{\circ} \mathrm{C}\right)$

Short Answer

Expert verified
a. 1 mole of \(\mathrm{H}_{2}\) at 100°C and 0.5 atm has a larger positional probability. b. 1 mole of \(\mathrm{N}_{2}\) at STP has a larger positional probability. c. 1 mole of \(\mathrm{H}_{2} \mathrm{O}(l)\) at 20°C has a larger positional probability.

Step by step solution

01

Case a: Comparing \(\mathrm{H}_{2}\) at STP and at 100°C, 0.5 atm

In this case, we need to compare 1 mole of \(\mathrm{H}_{2}\) at STP to 1 mole of \(\mathrm{H}_{2}\) at 100°C and 0.5 atm. Since higher temperatures and lower pressures lead to higher positional probabilities, let's compare both the conditions: 1. Temperature: At STP, the temperature is 0°C, while in the second case, it is 100°C. The second case has a higher temperature, which leads to higher positional probability. 2. Pressure: At STP, the pressure is 1 atm, while in the second case, it is 0.5 atm. The second case has lower pressure, which leads to higher positional probability. As both the temperature and pressure lead to higher positional probability in the second case, we can conclude that 1 mole of \(\mathrm{H}_{2}\) at 100°C and 0.5 atm has a larger positional probability than at STP.
02

Case b: Comparing \(\mathrm{N}_{2}\) at STP and at 100 K, 2.0 atm

Now, we need to compare 1 mole of \(\mathrm{N}_{2}\) at STP to 1 mole of \(\mathrm{N}_{2}\) at 100 K and 2.0 atm: 1. Temperature: At STP, the temperature is 273.15 K, while in the second case, it is 100 K. The first case has a higher temperature, which leads to higher positional probability. 2. Pressure: At STP, the pressure is 1 atm, while in the second case, it is 2.0 atm. The first case has lower pressure, which leads to higher positional probability. Since both the temperature and pressure lead to higher positional probability in the first case, we can conclude that 1 mole of \(\mathrm{N}_{2}\) at STP has a larger positional probability than at 100 K and 2.0 atm.
03

Case c: Comparing \(\mathrm{H}_{2} \mathrm{O}(s)\) at 0°C and \(\mathrm{H}_{2} \mathrm{O}(l)\) at 20°C

Finally, we need to compare 1 mole of \(\mathrm{H}_{2} \mathrm{O}(s)\) at 0°C to 1 mole of \(\mathrm{H}_{2} \mathrm{O}(l)\) at 20°C. In this case, we are comparing solid water (ice) to liquid water. It is important to note that the positional probability of particles in a liquid is higher than that of particles in a solid due to the increased freedom of movement in the liquid state. Since liquid water has a higher positional probability than solid water, we can conclude that 1 mole of \(\mathrm{H}_{2} \mathrm{O}(l)\) at 20°C has a larger positional probability than 1 mole of \(\mathrm{H}_{2} \mathrm{O}(s)\) at 0°C.

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Most popular questions from this chapter

In the text, the equation $$\Delta G=\Delta G^{\circ}+R T \ln (Q)$$ was derived for gaseous reactions where the quantities in \(Q\) were expressed in units of pressure. We also can use units of mol/L for the quantities in \(Q\)specifically for aqueous reactions. With this in mind, consider the reaction $$\mathrm{HF}(a q) \rightleftharpoons \mathrm{H}^{+}(a q)+\mathrm{F}^{-}(a q)$$ for which \(K_{\mathrm{a}}=7.2 \times 10^{-4}\) at \(25^{\circ} \mathrm{C}\) . Calculate \(\Delta G\) for the reaction under the following conditions at \(25^{\circ} \mathrm{C} .\) a. $[\mathrm{HF}]=\left[\mathrm{H}^{+}\right]=\left[\mathrm{F}^{-}\right]=1.0 \mathrm{M}$ b. $[\mathrm{HF}]=0.98 M,\left[\mathrm{H}^{+}\right]=\left[\mathrm{F}^{-}\right]=2.7 \times 10^{-2} M$ c. $[\mathrm{HF}]=\left[\mathrm{H}^{+}\right]=\left[\mathrm{F}^{-}\right]=1.0 \times 10^{-5} \mathrm{M}$ d. $[\mathrm{HF}]=\left[\mathrm{F}^{-}\right]=0.27 M,\left[\mathrm{H}^{+}\right]=7.2 \times 10^{-4} M$ e. $[\mathrm{HF}]=0.52 M,\left[\mathrm{F}^{-}\right]=0.67 M,\left[\mathrm{H}^{+}\right]=1.0 \times 10^{-3} \mathrm{M}$ Based on the calculated DG values, in what direction will the reaction shift to reach equilibrium for each of the five sets of conditions?

The deciding factor on why HF is a weak acid and not a strong acid like the other hydrogen halides is entropy. What occurs when HF dissociates in water as compared to the other hydrogen halides?

Which of the following reactions (or processes) are expected to have a negative value for \(\Delta S^{\circ} ?\) a. $\mathrm{SiF}_{6}(a q)+\mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{HF}(g)+\mathrm{SiF}_{4}(g)$ b. $4 \mathrm{Al}(s)+3 \mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{Al}_{2} \mathrm{O}_{3}(s)$ c. \(\mathrm{CO}(g)+\mathrm{Cl}_{2}(g) \longrightarrow \mathrm{COCl}_{2}(g)\) d. $\mathrm{C}_{2} \mathrm{H}_{4}(g)+\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(l)$ e. \(\mathrm{H}_{2} \mathrm{O}(s) \longrightarrow \mathrm{H}_{2} \mathrm{O}(l)\)

What information can be determined from \(\Delta G\) for a reaction? Does one get the same information from \(\Delta G^{\circ},\) the standard free energy change? \(\Delta G^{\circ}\) allows determination of the equilibrium constant \(K\) for a reaction. How? How can one estimate the value of \(K\) at temperatures other than \(25^{\circ} \mathrm{C}\) for a reaction? How can one estimate the temperature where \(K=1\) for a reaction? Do all reactions have a specific temperature where \(K=1 ?\)

It is quite common for a solid to change from one structure to another at a temperature below its melting point. For example, sulfur undergoes a phase change from the rhombic crystal structure to the monoclinic crystal form at temperatures above \(95^{\circ} \mathrm{C}\) a. Predict the signs of \(\Delta H\) and \(\Delta S\) for the process $\mathrm{S}_{\text { rhombic}}(s)\longrightarrow \mathrm{S}_{\text { monoclinic }}(s)$ b. Which form of sulfur has the more ordered crystalline structure (has the smaller positional probability)?

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