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प्रश्न
Define the Standard enthalpy of combustion.
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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.
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संबंधित प्रश्न
Calculate the total heat required
a) to melt 180 g of ice at 0 °C
b) heat it to 100 °C and then
c) vapourise it at that temperature.
[Given: ΔfusH° (ice) = 6.01 kJ mol-1 at 0 °C, ΔvapH° (H2O) = 40.7 kJ mol-1 at 100 °C, Specific heat of water is 4.18 J g-1 K-1]
The standard enthalpy of formation of water is - 286 kJ mol-1. Calculate the enthalpy change for the formation of 0.018 kg of water.
The enthalpy change of the following reaction:
\[\ce{CH_{4(g)} + Cl_{2(g)} -> CH3Cl_{(g)} + HCl_{(g)}ΔH^0 = –104 kJ}\]
Calculate C – Cl bond enthalpy. The bond enthalpies are:
| Bond | C − H | Cl − Cl | H − Cl |
| ∆H°/kJ mol−1 | 414 | 243 | 431 |
Define standard enthalpy of formation.
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 |
Define the Enthalpy of ionisation.
When 2 moles of C2H6(g) are completely burnt, 3129 kJ of heat is liberated. If ∆Hf for CO2(g) and H2O(l) are −395 and −286 kJ per mole respectively, the heat combustion of C2H6(g) is ____________.
A compound that has a high negative heat of formation is normally ____________.
The volume of oxygen required for complete combustion of 0.25 mole of methane at STP is ______.
The standard heats of formation in kcal mol−1 of NO2(g) and N2O4(g) are 8.0 and 2.0 respectively. The heat of dimerization of NO2 in kcal is ____________.
\[\ce{2NO2_{(g)} ⇌ N2O4_{(g)}}\]
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:
\[\ce{S + 3/2O2 -> SO3 +2{x} kcal}\] .........(i)
\[\ce{SO2 + 1/2O2 -> SO3 + {y} kcal}\] .......(ii)
The heat of formation of SO2 is ____________.
The heat evolved in the combustion of benzene is given by
\[\ce{C6H6 + 7 1/2O2 -> 6CO2_{(g)} + 3H2O_{(l)}}\]; ΔH = −3264.6 kJ
Which of the following quantities of heat energy will be evolved when 39 g C6H6 are burnt?
Calculate the enthalpy of hydrogenation of C2H4(g), given that the enthalpy of formation of ethane and ethylene are −30.2 kcal and +12.5 kcal respectively.
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 ________.
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)?
Heat of formation of ethane, ethylene acetylene and carbon dioxide are - 136, - 66, - 228 and - 395 (all in kJ) respectively, most stable among them is ______.
Calculate the standard enthalpy of formation of CH3OH(l) from the following data:
- \[\ce{CH3OH_{(l)} + 3/2 O2_{(g)} -> CO2_{(g)} + 2H2O_{(l)}ΔH^° = - 726 kJ mol^{-1}}\]
- \[\ce{C_{(s)} + O2_{(g)} → CO2_{(g)}Δ_cH^° = – 393 kJ mol^{-1}}\]
- \[\ce{H2_{(g)} + 1/2 O2_{(g)} -> H2O_{(l)}Δ_fH^° = - 286 kJ mol^{-1}}\]
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:
\[\begin{array}{cc}
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{...................}\ce{H}\phantom{...}\ce{H}\phantom{....}\\
\phantom{.}|\phantom{....}|\phantom{....................}|\phantom{....}|\phantom{.....}\\
\ce{C = C + H - H -> H - C - C - H}\\
\phantom{.}|\phantom{....}|\phantom{....................}|\phantom{....}|\phantom{.....}\\
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{...................}\ce{H}\phantom{...}\ce{H}\phantom{....}
\end{array}\]
What is enthalpy of formation of NH3 if bond enthalpies as (N ≡ N) = - 941 kJ/mol.
\[\ce{(H - H)}\] = 436 kJ/mol and \[\ce{(N - H)}\] = 389 kJ/mol?
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)
The heat evolved in the combustion of 6.022 x 1021 carbon particles is 3.94 kJ. The heat of combustion of carbon is ______.
Calculate heat evolved for combustion of 13 gm of acetylene (C2H2).
Given: \[\ce{C2H2_{(g)} + 5/2O_{2(g)}-> 2CO_{2(g)} + H2O_{(l)} \Delta_{(c)}H^{0} = - 1300 kJ}\]
Heat of combustion of CH4(g) is -890 kJ/mole. What is the value of Δc H of 8gm of methane?
Calculate the standard enthalpy of combustion of methane if the standard enthalpy of formation of methane, carbon dioxide and water are −74.8, −393.5 and −285.8 kJmol−1 respectively.
