Advertisements
Advertisements
प्रश्न
Answer the following question.
State Hess’s law of constant heat summation. Illustrate with an example. State its applications.
Advertisements
उत्तर
1. Hess’s law of constant heat summation:
Hess’s law of constant heat summation states that “Overall the enthalpy change for a reaction is equal to the sum of enthalpy changes of individual steps in the reaction”.
2. Illustration:
- The enthalpy change for a chemical reaction is the same regardless of the path by which the reaction occurs. Hess’s law is a direct consequence of the fact that enthalpy is a state function. The enthalpy change of a reaction depends only on the initial and final states and not on the path by which the reaction occurs.
- To determine the overall equation of the reaction, reactants and products in the individual steps are added or subtracted like algebraic entities.
- Consider the synthesis of NH3,
- \[\ce{2H_{2(g)} + N_{2(g)} → N2H_{4(g)}, Δ_r H^0_1 = + 95.4 kJ}\]
- \[\ce{N2H_{4(g)} + H_{2(g)} → 2NH_{3(g)}, Δ_r H^0_2 = -187.6 kJ}\]
\[\ce{H_{2(g)} + N_{2(g)} → 2NH_{3(g)}, Δ_rH^0 = - 92.2 kJ}\]
The sum of the enthalpy changes for steps (1) and (2) is equal to the enthalpy change for the overall reaction.
3. Application of Hess’s law:
The Hess's law has been useful to calculate the enthalpy changes for the reactions with their enthalpies being not known experimentally. To calculate heat of formation, combustion, neutralization, ionization, etc.
संबंधित प्रश्न
Answer the following question.
Calculate ΔrH° for the following reaction at 298 K:
1) 2H3BO3(aq) → B2O3(s) + 3H2O(l), ΔrH° = + 14.4 kJ
2) H3BO3(aq) → HBO2(aq) + H2O(l), ΔrH° = - 0.02 kJ
3) H2B4O7(s) → 2B2O3(s) + H2O(l), ΔrH° = + 17.3 kJ
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.
Calculate the standard enthalpy of combustion of CH4(g) if ΔfH°(CH4) = – 74.8 kJ mol–1, ΔfH°(CO2) = – 393.5 kJ mol–1 and ΔfH°(H2O) = – 285.8 kJ mol–1.
Define the Enthalpy of ionisation.
Write an application of Hess’s law.
Classify the following into intensive and extensive properties.
Pressure, volume, mass, temperature.
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 ____________.
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)?
The heat of formations of CO(g) and CO2(g) are −26.4 kcal and −94.0 kcal respectively. The heat of combustion of carbon monoxide will be ____________.
Daily requirement of energy of a person is 'x' kJ. If heat of combustion of food material (Molecular mass = 100 g) is 'y' kJ, his daily consumption of the food in gram would be ____________.
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 ____________.
\[\ce{2NO2_{(g)} ⇌ N2O4_{(g)}}\]
The enthalpy change accompanying a reaction in which 1 mole of the substance in the standard state reacts completely with oxygen or is completely burnt is called as ____________.
\[\ce{S + 3/2O2 -> SO3 +2{x} kcal}\] .........(i)
\[\ce{SO2 + 1/2O2 -> SO3 + {y} kcal}\] .......(ii)
The heat of formation of SO2 is ____________.
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.
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 ________.
Heat of formation of water is - 272 kJ mol-1. What quantity of water is converted to H2 and O2 by 750 kJ of heat?
Which of the following equations has ΔfH° and ΔH° same?
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 ______.
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 the amount of water formed by the combustion of 1.6 g methane?
When the enthalpy of combustion of carbon to carbon dioxide is - 360 kJ mol-1, then the enthalpy change for the formation of 18 g of CO2 from carbon and dioxygen at the same temperature in kJ will be ______.
The enthalpy change that accompanies a reaction in which 1 mole of its standard state is formed from its elements in their standard states
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
For the reaction, H2 + I2 ⇌ 2HI; ΔH = 12.4 kcal. The heat of formation of HI, ΔHf = ______.
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.
Calculate heat evolved for combustion of 13 gm of acetylene (C2H2).
Given: \[\ce{C2H2_{(g)} + 5/2O_{2(g)}-> 2CO_{2(g)} + H2O_{(l)} \Delta_{(c)}H^{0} = - 1300 kJ}\]
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.
