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 in brief.
What is the standard enthalpy of combustion? Give an example.
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.
Define the Standard enthalpy of combustion.
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 |
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 Bond enthalpy.
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 for CCl4(g), H2O(g), CO2(g), and HCl(g) are −25.5, −57.8, −94.1 and −22.1 kcal mol−1, respectively.
∆H for the reaction
\[\ce{CCl4_{(g)} + 2H2O_{(g)} -> CO2_{(g)} + 4HCl_{(g)}}\] at 298 K
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:
Enthalpy of formation of two compounds x and y are −84 kJ and −156 kJ respectively. Which of the following statements is CORRECT?
Given the reaction,
\[\ce{CH2O_{(g)} + O2_{(g)} -> CO2_{(g)} + H2O_{(g)}}\] ΔH = −527 kJ
How much heat will be evolved in the formation of 60 g of CO2?
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.
Combustion of glucose takes place as
\[\ce{C6H12O6_{(s)} + 6O2_{(g)} -> 6CO2_{(g)} + 6H2O_{(g)}}\]; ΔH = −72 kcal mol−1
The energy needed for the production of 1.8 g of glucose by photosynthesis will be ___________.
The enthalpy of formation of nitrogen dioxide is +33.2 kJ mol−1. The enthalpy of the reaction \[\ce{2N2_{(g)} + 4O2_{(g)} -> 4NO2_{(g)}}\]; is ____________.
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 ________.
\[\ce{A -> B}\], ∆H = −10 kJ mol−1, Ea(f) = 50 kJ mol−1, then Ea of \[\ce{B -> A}\] will be ______.
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)
Define and explain the term, enthalpy of reaction.
Standard enthalpy of combustion of a substance is given. Then Write thermochemical equation.
ΔcH0[CH3CHO(l)] = - 1166 kJ mol-1
Draw energy profile diagram and show:
- activated complex
- energy of activation for forward and backward reactions
- enthalpy of reaction
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 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.
