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प्रश्न
Answer in brief.
What is the standard enthalpy of combustion? Give an example.
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उत्तर
- The standard enthalpy of combustion of a substance is the standard enthalpy change accompanying a reaction in which one mole of the substance in its standard state is completely oxidised.
- Consider the reaction,
C2H2(g) + `5/2` O2(g) → 2CO2(g) + H2O(l), Δr H° = - 1300 kJ
In the above reaction, the standard enthalpy change of the oxidation reaction, –1300 kJ is the standard enthalpy of combustion of C2H2(g).
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संबंधित प्रश्न
Answer in brief.
How much heat is evolved when 12 g of CO reacts with NO2? The reaction is:
4CO(g) 2NO2(g) → 4CO2(g) + N2(g), ΔrH° = - 1200 kJ
The enthalpy change for the reaction, \[\ce{C2H4_{(g)} + H2_{(g)} -> C2H6_{(g)}}\] is −620 J when 100 mL of ethylene and 100 ml of \[\ce{H2}\] react at 1 bar pressure. Calculate the pressure volume type of work and ΔU for the reaction.
Calculate enthalpy of formation of HCl if bond enthalpies of H2, Cl2 and HCl are 434 kJ mol-1, 242 kJ mol–1 and 431 kJ mol–1 respectively.
Define the Standard enthalpy of combustion.
State and explain Hess’s law of constant heat summation.
Define standard enthalpy of formation.
Calculate the standard enthalpy of formation of liquid methanol from the following data:
- \[\ce{CH3OH_{(l)} + \frac{3}{2} O_{2(g)} -> CO_{2(g)} + 2H2O_{(l)}}\] ∆H° = – 726 kJ mol–1
- \[\ce{C_{(Graphite)} + O_{2(g)} -> CO_{2(g)}}\] ∆cH° = – 393 kJ mol–1
- \[\ce{H_{2(g)} + \frac{1}{2} O_{2(g)} -> H2O_{(l)}}\] ∆fH° = – 286 kJ mol–1
Define the Bond enthalpy.
Calculate the standard enthalpy of the reaction.
\[\ce{2Fe_{(s)} + \frac{3}{2} O_{2(g)} -> Fe2O_{3(s)}}\]
Given:
| 1. | \[\ce{2Al_{(s)} + Fe2O_{3(s)} -> 2Fe_{(s)} + Al_2O_{3(s)}}\], | ∆rH° = –847.6 kJ |
| 2. | \[\ce{2Al_{(s)} + \frac{3}{2} O_{2(g)} -> Al2O_{3(s)}}\], | ∆rH° = –1670 kJ |
Does the following reaction represent a thermochemical equation?
\[\ce{CH_{4(g)} + 2O_{2(g)} -> CO_{2(g)} + 2H2O_{(g)}}\], ∆fH° = –900 kJ mol–1
Classify the following into intensive and extensive properties.
Pressure, volume, mass, temperature.
The volume of oxygen required for complete combustion of 0.25 mole of methane at STP is ______.
When 6.0 g of graphite reacts with dihydrogen to give methane gas, 37.4 kJ of heat is liberated. What is standard enthalpy of formation of CH4 (g)?
lf, \[\ce{C_{(s)} + O2_{(g)} -> CO2_{(g)}}\], ∆H = x .........(i)
\[\ce{CO_{(g)} + 1/2O2_{(g)} -> CO2_{(g)}}\], ∆H = y .......(ii)
Then, the heat of formation of CO is:
Which of the following compounds is Not present in its standard state at 25°C and 1 atmosphere pressure?
Standard enthalpy of formation of water is - 286 kJ mol-1. When 1800 mg of water is formed from its constituent elements in their standard states the amount of energy liberated is ______.
Given that,
\[\ce{C_{(s)} + O_{2(g)} -> CO_{2(g)}}\] ΔH° = -X kJ
\[\ce{2CO_{(g)} + O_{2(g)} -> 2CO_{2(g)}}\] ΔH° = - Y kJ, then standard enthalpy of formation of carbon monoxide is ________.
An ideal gas expands isothermally and reversibly from 10 m3 to 20 m3 at 300 K performing 5 .187 kJ of work on surrounding. Calculate number of moles of gas undergoing expansion. (R = 8.314 J K-1 mol-1)
Standard entropies of N2(g), H2(g), and NH3(g) are a1, a2 and a3 J K-1 mol-1 respectively. What is value of ΔS° for formation of NH3(g)?
Calculate the standard enthalpy of:
\[\ce{N2H_{4(g)} + H_{2(g)} -> 2NH_{3(g)}}\]
If ΔH0(N – H) = 389 kJ mol–1, ΔH0(H – H) = 435 kJ mol–1, ΔH0(N – N) = 159 kJ mol–1.
From the following bond energies:
H – H bond energy: 431.37 kJ mol−1
C = C bond energy: 606.10 kJ mol−1
C – C bond energy: 336.49 kJ mol−1
C – H bond energy: 410.50 kJ mol−1
Enthalpy for the given reaction will be:
\[\begin{array}{cc}
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{...................}\ce{H}\phantom{...}\ce{H}\phantom{....}\\
\phantom{.}|\phantom{....}|\phantom{....................}|\phantom{....}|\phantom{.....}\\
\ce{C = C + H - H -> H - C - C - H}\\
\phantom{.}|\phantom{....}|\phantom{....................}|\phantom{....}|\phantom{.....}\\
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{...................}\ce{H}\phantom{...}\ce{H}\phantom{....}
\end{array}\]
When 0.5 gram of sulphur is burnt to form SO2, 4.6 kJ of heat liberated. Calculate enthalpy of formation of SO2(g). (Atomic mass : S = 32, O = 16)
Calculate the standard enthalpy of the reaction, \[\ce{SiO2_{(s)} + 3C_{(graphite)} -> SiC_{(s)} + 2CO_{(g)}}\] from the following reactions:
- \[\ce{Si_{(s)} + O2_{(g)} -> SiO2_{(s)}}\], ΔrH0 = −911 kJ
- \[\ce{2C_{(graphite)} + O2_{(g)} -> 2CO_{(g)}}\], ΔrH0 = −221 kJ
- \[\ce{Si_{(s)} + C_{(graphite)} -> SiC_{(s)}}\], ΔrH0 = −65.3 kJ
Draw energy profile diagram and show:
- activated complex
- energy of activation for forward and backward reactions
- enthalpy of reaction
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Calculate ΔsubH of the H2O from the given data:
\[\ce{H2O_{(s)}->H2O_{(l)},}\] ΔfusH = 6.01kJ mol−1
\[\ce{H2O_{(l)}-> H2O_{(g)},}\] ΔVapH = 45.07 kJ mol−1.
Heat of combustion of CH4(g) is -890 kJ/mole. What is the value of Δc H of 8gm of methane?
