Answer:
A. ΔG° = 132.5 kJ
B. ΔG° = 13.69 kJ
C. ΔG° = -58.59 kJ
Explanation:
Let's consider the following reaction.
CaCO₃(s) → CaO(s) + CO₂(g)
We can calculate the standard enthalpy of the reaction (ΔH°) using the following expression.
ΔH° = ∑np . ΔH°f(p) - ∑nr . ΔH°f(r)
where,
n: moles
ΔH°f: standard enthalpy of formation
ΔH° = 1 mol × ΔH°f(CaO(s)) + 1 mol × ΔH°f(CO₂(g)) - 1 mol × ΔH°f(CaCO₃(s))
ΔH° = 1 mol × (-635.1 kJ/mol) + 1 mol × (-393.5 kJ/mol) - 1 mol × (-1206.9 kJ/mol)
ΔH° = 178.3 kJ
We can calculate the standard entropy of the reaction (ΔS°) using the following expression.
ΔS° = ∑np . S°p - ∑nr . S°r
where,
S: standard entropy
ΔS° = 1 mol × S°(CaO(s)) + 1 mol × S°(CO₂(g)) - 1 mol × S°(CaCO₃(s))
ΔS° = 1 mol × (39.75 J/K.mol) + 1 mol × (213.74 J/K.mol) - 1 mol × (92.9 J/K.mol)
ΔS° = 160.6 J/K. = 0.1606 kJ/K.
We can calculate the standard Gibbs free energy of the reaction (ΔG°) using the following expression.
ΔG° = ΔH° - T.ΔS°
where,
T: absolute temperature
<h3>A. 285 K</h3>
ΔG° = ΔH° - T.ΔS°
ΔG° = 178.3 kJ - 285K × 0.1606 kJ/K = 132.5 kJ
<h3>B. 1025 K</h3>
ΔG° = ΔH° - T.ΔS°
ΔG° = 178.3 kJ - 1025K × 0.1606 kJ/K = 13.69 kJ
<h3>C. 1475 K</h3>
ΔG° = ΔH° - T.ΔS°
ΔG° = 178.3 kJ - 1475K × 0.1606 kJ/K = -58.59 kJ
Answer:
A
Explanation:
its a because that is the first thing you do
Answer:
Mass of original sample = 100 g
Explanation:
Half life of cesium-137 = 30.17 years
Where, k is rate constant
So,
The rate constant, k = 0.02297 year⁻¹
Time = 90.6 years
Using integrated rate law for first order kinetics as:
Where,
is the concentration at time t
is the initial concentration
Initial concentration
= ?
Final concentration
= 12.5 grams
Applying in the above equation, we get that:-
![[A_0]=\frac{12.5}{e^{-0.02297\times 90.6}}\ g=100\ g](https://tex.z-dn.net/?f=%5BA_0%5D%3D%5Cfrac%7B12.5%7D%7Be%5E%7B-0.02297%5Ctimes%2090.6%7D%7D%5C%20g%3D100%5C%20g)
<u>Mass of original sample = 100 g</u>
To find the mole of a substance, you take the mass divided by the molar mass of that substance~