Answer:
(a) Cgas = 0.125 kJ/k
(b) cgas = 0.25kJ/kg.K
(c) cm(gas) = 0.021kJ/mol.K
Explanation:
18.9 kJ is equal to the sum of the heat absorbed by the gas and the heat absorbed by the calorimeter.
Qcal + Qgas = 18.9 kJ [1]
We can calculate the heat absorbed using the following expression.
Q = C . ΔT
where,
C is the heat capacity
ΔT is the change in the temperature
<em>(a) What is the heat capacity of the sample?</em>
From [1],
Ccal . ΔT + Cgas . ΔT = 18.9 kJ
(2.22kJ/K) × 8.06 K + Cgas × 8.06 K = 18.9 kJ
Cgas = 0.125 kJ/k
<em>(b) If the sample has a mass of 0.5 kilograms, what is the specific heat capacity of the substance?</em>
We can calculate the specific heat capacity (c) using the following expression:

<em>(c) If the sample is Krypton, what is the molar heat capacity at constant volume of Krypton? The molar mass of Krypton is 83.8 grams/mole.</em>
The molar heat capacity is:

Yes the particles are larger than 10,000 Angstroms which allow it to be separated by filtration
Answer:
A i. Internal energy ΔU = -4.3 J ii. Internal energy ΔU = -6.0 J B. The second system is lower in energy.
Explanation:
A. We know that the internal energy,ΔU = q + w where q = quantity of heat and w = work done on system.
1. In the above q = -7.9 J (the negative indicating heat loss by the system). w = 3.6 J (It is positive because work is done on the system). So, the internal energy for this system is ΔU₁ = q + w = -7.9J + 3.6J = -4.3 J
ii. From the question q = +1.5 J (the positive indicating heat into the system). w = -7.5 J (It is negative because work is done by the system). So, the internal energy for this system is ΔU₂ = q + w = +1.5J + (-7.5J) = +1.5J - 7.5J = - 6.0J
B. We know that ΔU = U₂ - U₁ where U₁ and U₂ are the initial and final internal energies of the system. Since for the systems above, the initial internal energies U₁ are the same, then we say U₁ = U. Let U₁ and U₂ now represent the final energies of both systems in A i and A ii above. So, we write ΔU₁ = U₁ - U and ΔU₂ = U₂ - U where ΔU₁ and ΔU₂ are the internal energy changes in A i and A ii respectively. Now from ΔU₁ = U₁ - U, U₁ = ΔU₁ + U and U₂ = ΔU₂ + U. Subtracting both equations U₁ - U₂ = ΔU₁ - ΔU₂
= -4.3J -(-6.0 J)= 1.7 J. Since U₁ - U₂ > 0 , U₂ < U₁ , so the second system's internal energy increase less and is lower in energy and is more stable.
I think it’s hydroxybutanal
Answer:
- Add AgNO₃ solution to both unlabeled flasks: based on solubility rules, you can predict that when you add AgNO₃ to the NaCl solution, you will obtain AgCl precipitate, while no precipitate will be formed from the NaClO₃ solution.
Explanation:
<u>1. Adding AgNO₃ to NaCl solution:</u>
- AgNO₃ (aq) + NaCl (aq) → AgCl (s) + NaNO₃ (aq)
<u>2. Adding AgNO₃ to NaClO₃ solution</u>
- AgNO₃ (aq) + NaClO₃ (aq) → AgClO₃ (aq) + NaNO₃ (aq)
<u />
<u>3. Relevant solubility rules for the problem.</u>
- Although most salts containing Cl⁻ are soluble, AgCl is a remarkable exception and is insoluble.
- All chlorates are soluble, so AgClO₃ is soluble.
- Salts containing nitrate ion (NO₃⁻) are generally soluble and NaNO₃ is not an exception to this rule. In fact, NaNO₃ is very well known to be soluble.
Hence, when you add AgNO₃ to the NaCl solution the AgCl formed will precipitate, and when you add the same salt (AgNO₃) to the AgClO₃ solution both formed salts AgClO₃ and NaNO₃ are soluble.
Then, the precipiate will permit to conclude which flask contains AgCl.