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Answer the following question. State Hess’s law of constant heat summation. Illustrate with an example. State its applications. - Chemistry

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प्रश्न

Answer the following question.

State Hess’s law of constant heat summation. Illustrate with an example. State its applications.

थोडक्यात उत्तर
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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,
  1. \[\ce{2H_{2(g)} + N_{2(g)} → N2H_{4(g)}, Δ_r H^0_1 = + 95.4 kJ}\]
  2. \[\ce{N2H_{4(g)} + H_{2(g)} → 2NH_{3(g)}, Δ_r H^0_2 = -187.6 kJ}\]
                                                                                              
    \[\ce{H_{2(g)} + N_{2(g)} → 2NH_{3(g)}, Δ_rH^0 = - 92.2 kJ}\]

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.

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Thermochemistry
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पाठ 4: Chemical Thermodynamics - Exercises [पृष्ठ ८८]

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बालभारती Chemistry [English] Standard 12 Maharashtra State Board
पाठ 4 Chemical Thermodynamics
Exercises | Q 4.03 | पृष्ठ ८८

संबंधित प्रश्‍न

Select the most appropriate option.

Which of the following reactions is exothermic?


Answer the following in one or two sentences.

What is standard state of a substance?


Answer in brief.

How will you calculate reaction enthalpy from data on bond enthalpies?


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 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 Bond enthalpy.


Define the Enthalpy of ionisation.


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)?


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 ____________.

\[\ce{2NO2_{(g)} ⇌ N2O4_{(g)}}\]


\[\ce{S + 3/2O2 -> SO3 +2{x} kcal}\] .........(i)

\[\ce{SO2 + 1/2O2 -> SO3 + {y} kcal}\] .......(ii)

The heat of formation of SO2 is ____________.


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\[\ce{C6H6 + 7 1/2O2 -> 6CO2_{(g)} + 3H2O_{(l)}}\]; ΔH = −3264.6 kJ

Which of the following quantities of heat energy will be evolved when 39 g C6H6 are burnt?


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\[\ce{CH2O_{(g)} + O2_{(g)} -> CO2_{(g)} + H2O_{(g)}}\] ΔH = −527 kJ

How much heat will be evolved in the formation of 60 g of CO2?


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Which of the following equations has ΔfH° and ΔH° same?


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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:

\[\begin{array}{cc}
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{...................}\ce{H}\phantom{...}\ce{H}\phantom{....}\\
\phantom{.}|\phantom{....}|\phantom{....................}|\phantom{....}|\phantom{.....}\\
\ce{C = C + H - H -> H - C - C - H}\\
\phantom{.}|\phantom{....}|\phantom{....................}|\phantom{....}|\phantom{.....}\\
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{...................}\ce{H}\phantom{...}\ce{H}\phantom{....}
\end{array}\]


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\[\ce{H2O_{(l)}-> H2O_{(g)},}\] ΔVapH = 45.07 kJ mol−1.


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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.


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