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Figure 1 shows an incomplete Born-Haber cycle for the formation of caesium iodide - AQA - A-Level Chemistry - Question 1 - 2019 - Paper 1

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Figure 1 shows an incomplete Born-Haber cycle for the formation of caesium iodide. The diagram is not to scale. Cs(g) + rac{1}{2} I_2(g) Csl(s) Table 1 gives val... show full transcript

Worked Solution & Example Answer:Figure 1 shows an incomplete Born-Haber cycle for the formation of caesium iodide - AQA - A-Level Chemistry - Question 1 - 2019 - Paper 1

Step 1

Complete Figure 1 by writing the formulas, including state symbols, of the appropriate species on each of the two blank lines.

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Answer

Top line: Cs(g) + rac{1}{2} I_2(g) Lower line: CsI(s)

Step 2

Use Figure 1 and the data in Table 1 to calculate the standard enthalpy of atomisation of iodine.

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Answer

Using Hess’s law, we can write the following equation:

ΔH° = ΔH(a) + 376 + (-314) + (-585) + 337

Substituting the values from the table:

ΔH° = ΔH(a) + 376 - 314 - 585 + 337 = ΔH(a) + 107 kJ/mol

Given that the standard enthalpy change for the entire reaction when forming caesium iodide is approximately zero, the value for the enthalpy of atomisation of iodine calculates to:

ΔH(a) = -107 kJ/mol.

Step 3

The enthalpy of lattice formation for caesium iodide in Table 1 is a value obtained by experiment. Deduced what these values indicate about the bonding in caesium iodide.

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Answer

The calculated lattice formation value of -582 kJ/mol suggests a strong ionic character in the bonding of caesium iodide. On the other hand, the experimental value of -585 kJ/mol indicates the real-world stability and strong interaction between Cs extsuperscript{+} and I extsuperscript{-}, showing that the bonding is almost entirely ionic, rather than having significant covalent character.

Step 4

Use data from Table 2 to show that this reaction is not feasible at 298 K.

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Answer

To determine whether the reaction is feasible at 298 K, we can calculate the change in Gibbs free energy (ΔG):

ΔG = ΔH - TΔS

From Table 2:

ext{ΔS} = ((82.8 + 117) - 130) = 69.8 	ext{ J K}^{-1} 	ext{ mol}^{-1}

Converting this to kJ:

ΔS = 0.0698 ext{ kJ K}^{-1} ext{ mol}^{-1}

Calculating ΔG:

ΔG = 337 kJ/mol - (298 K × 0.0698 kJ K⁻¹ mol⁻¹) ΔG = 337 kJ/mol - 20.8 kJ/mol = 316.2 kJ/mol

Since ΔG > 0, the reaction is not feasible at 298 K.

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