1. The temperature at which the given reaction is in equilibrium is:
\(\mathrm{X_{(g)} +3Y_{(g)} \rightleftharpoons 2Z_{(g)} ; \Delta H= -40~ kJ ~mol^{-1}}~\)
(The standard entropies of X, Y, and Z are 60, 40, and 50 J K–1 mol–1, respectively.)
1. 273 K
2. 600 K
3. 500 K
4. 400 K
2. Which one of the following reactions obeys ∆H ≠ ∆E?
| 1. |
H 2 (g) + I 2 (g) ⇌ 2 HI (g) |
| 2. |
HCl (aq) + NaOH (aq)→ NaCl (aq) + H2O (l) |
| 3. |
C (s) + O2 (g) ⇌ CO2 (g) |
| 4. |
N2 (g) + 3H2 (g) → 2NH3 (g) |
3. Match the items given in Column I with those given in Column II:
|
Column I |
|
Column II |
| A. |
Temperature |
i. |
Path function |
| B. |
Free energy |
ii. |
State function |
| C. |
Heat |
|
|
| D. |
Work |
|
|
| Options |
(A) |
(B) |
(C) |
(D) |
| 1. |
i |
ii |
ii |
i |
| 2. |
ii |
ii |
i |
i |
| 3. |
i |
i |
ii |
i |
| 4. |
ii |
ii |
ii |
i |
4. Which of the following options correctly represents the relationship between \(C_p \text { and } C_V\) for one mole of an ideal gas?
| 1. |
\(C_P=R C_V \) |
2. |
\(C_V=RC_P \) |
| 3. |
\(C_P+C_V=R \) |
4. |
\(C_{{P}}-{C}_{{V}}={R}\) |
5.
| Assertion (A) |
Absolute values of the internal energy of substances cannot be determined. |
| Reason (R) |
It is impossible to determine the exact values of constituent energies of the substances. |
| 1. |
Both (A) and (R) are True and (R) is the correct explanation of (A). |
| 2. |
Both (A) and (R) are True but (R) is not the correct explanation of (A). |
| 3. |
(A) is True but (R) is False. |
| 4. |
Both (A) and (R) are False. |
6. The enthalpy of a system increases by 50 kJ when its internal energy is increased by 113 kJ. What is the pressure in kNm-2 of the system if the volume of gas is reduced by 10 m3 at constant pressure?
[Given: 1 J = 1Nm]
1. 16.13
2. 6.30
3. 5.00
4. 30.30
7.
Five moles of an ideal gas at 1 bar and 298 K undergo free expansion (expansion into vacuum) such that its volume becomes double. Calculate the work done during the process:
1.
\( \mathrm{C}_{\mathrm{V}}\left(\mathrm{T}_2-\mathrm{T}_1\right)\)
2.
\( \text {-RT }\left(\mathrm{V}_2-\mathrm{V}_1\right) \)
3.
\( \text {-RT } \ln \mathrm({V}_1 / \mathrm{V}_2 )\)
4. Zero
8. What is the enthalpy change (ΔH) for the following reaction?
\(\mathrm {H}_2 \mathrm{C} = \mathrm {CH}_2 \text {(g)}+\mathrm{H}_2 \text {(g)} \rightarrow\mathrm {H}_3 \mathrm {C} - \mathrm {CH}_3 \text {(g)}\)
(Use the following bond energy data:
H-C: 413 kJ/mole
H-H: 436 kJ/mole
C=C: 614 kJ/mole
C-C: 348 kJ/ mole )
1. -656 kJ/mole
2. -343 kJ/mole
3. -289 kJ/mole
4. -124 kJ/mole
9. For a given chemical reaction A ⇌ B at \(\text 300 ~ \text K\), the free energy change is \(– 49.4~\mathrm{kJ ~mol^{–1}}\) and the enthalpy of reaction is \(51.4~\mathrm{kJ~ mol^{–1} }\). The entropy change of the reaction is:
1. \(140 ~\mathrm{JK^{–1} mol^{–1}}\)
2. \(671~\mathrm{JK^{–1} mol^{–1}}\)
3. \(336~\mathrm{JK^{–1} mol^{–1}}\)
4. \(390 ~\mathrm{JK^{–1} mol^{–1}}\)
10. What is the entropy change for the vaporization of water, if the molar heat of vaporization of water is \( +43.9~\text{kJ}\ mol^{-1}\) ?
1. \(8.49 \mathrm{~J} \mathrm{~mol}^{-1} \mathrm{~K}^{-1}\)
2. \(4.184 \mathrm{~J} \mathrm{~mol}^{-1} \mathrm{~K}^{-1}\)
3. \(2.78 \mathrm{~J} \mathrm{~mol}^{-1} \mathrm{~K}^{-1}\)
4. \(118 \mathrm{~J} \mathrm{~mol}^{-1} \mathrm{~K}^{-1}\)
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