Home
Class 12
CHEMISTRY
The difference between DeltaH and Delta...

The difference between `DeltaH and DeltaU (DeltaH - DeltaU)`, when the combustion of one mole of heptane (l ) is carried out at a temperature T, is equal to: `–xRT`. The value of x is_____.

A

`-4 RT`

B

`4 RT`

C

`-3 RT`

D

`3 RT`

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem, we need to find the value of \( x \) in the equation \( \Delta H - \Delta U = -xRT \) for the combustion of one mole of heptane. ### Step-by-Step Solution: 1. **Understand the Definitions**: - \( \Delta H \) is the change in enthalpy (heat content) at constant pressure. - \( \Delta U \) is the change in internal energy at constant volume. 2. **Use the Relationship Between \( \Delta H \) and \( \Delta U \)**: - The relationship is given by the formula: \[ \Delta H = \Delta U + \Delta N_g RT \] - Here, \( \Delta N_g \) is the change in the number of moles of gas during the reaction, \( R \) is the universal gas constant, and \( T \) is the temperature in Kelvin. 3. **Write the Combustion Reaction for Heptane**: - The combustion of heptane (\( C_7H_{16} \)) can be represented as: \[ C_7H_{16} + 11 O_2 \rightarrow 7 CO_2 + 8 H_2O \] - In this reaction, 1 mole of heptane reacts with 11 moles of oxygen to produce 7 moles of carbon dioxide and 8 moles of water. 4. **Calculate \( \Delta N_g \)**: - Count the number of moles of gaseous reactants and products: - Reactants: \( 11 \) moles of \( O_2 \) (since \( C_7H_{16} \) is a liquid and does not contribute to \( \Delta N_g \)). - Products: \( 7 \) moles of \( CO_2 \) (water is in liquid form and does not contribute). - Therefore: \[ \Delta N_g = \text{moles of gaseous products} - \text{moles of gaseous reactants} = 7 - 11 = -4 \] 5. **Substitute \( \Delta N_g \) into the Relationship**: - Now, substitute \( \Delta N_g \) into the equation: \[ \Delta H - \Delta U = \Delta N_g RT = -4RT \] 6. **Identify the Value of \( x \)**: - From the equation \( \Delta H - \Delta U = -xRT \), we can see that: \[ -xRT = -4RT \] - Thus, we find that: \[ x = 4 \] ### Final Answer: The value of \( x \) is **4**.

To solve the problem, we need to find the value of \( x \) in the equation \( \Delta H - \Delta U = -xRT \) for the combustion of one mole of heptane. ### Step-by-Step Solution: 1. **Understand the Definitions**: - \( \Delta H \) is the change in enthalpy (heat content) at constant pressure. - \( \Delta U \) is the change in internal energy at constant volume. ...
Promotional Banner

Topper's Solved these Questions

  • THERMOCHEMISTRY

    VMC MODULES ENGLISH|Exercise JEE ADVANCED (ARCHIVE)|31 Videos
  • THERMOCHEMISTRY

    VMC MODULES ENGLISH|Exercise LEVEL-2|65 Videos
  • THEORY OF SOLUTIONS

    VMC MODULES ENGLISH|Exercise JEE Advanced (Archive)|31 Videos
  • THERMODYNAMICS

    VMC MODULES ENGLISH|Exercise JEE ADVANCED (ARCHIVE)|44 Videos

Similar Questions

Explore conceptually related problems

What is the value of DeltaH-DeltaU for the combustion of Heptane (l) ?

DeltaU^(@) of combustion of CH_(4(g)) at certain temperature is -"393 kJ mol"^(-1) . The value of DeltaH^(@) is

Free energy, G=H-TS, is a state function that includes whether a reaction is spontaneous or non-spontaneous. If you think of TS as the part of the system's energy that is disordered already, then (H-TS) is the part of the system's energy that is still ordered and therefore free to cause spontaneous change by becoming disordered. Also, DeltaG=DeltaH-TDeltaS To see what this equation for free energy change has to do with spontaneity let us return to relationship. DeltaS_("total")=DeltaS_("sys")+DeltaS_("surr") = DeltaS + DeltaS_("surr") (It is generally understood that symbols without subscript refer to the system not the surroundings.) DeltaS_("surr")=-(DeltaH)/T , where DeltaH is the heat gained by then system at constant pressure. DeltaS_("total") = DeltaS -(DeltaH)/T rArr TDeltaH_("total")=DeltaH-TDeltaS rArr -TDeltaS_("total") =DeltaH-TDeltaS i.e. DeltaG=-TDeltaS_("total") From second law of thermodynamics, a reaction is spontaneous if DeltaS_("total") is positive, non-spontanous if DeltaS_("total") is negative and at equilibrium if DeltaS_("total") is zero. Since, -TDeltaS=DeltaG and since DeltaG and DeltaS have opposite signs, we can restate the thermodynamic criterion for the spontaneity of a reaction carried out at constant temperature and pressure. If DeltaG lt 0 , the reaction is spontaneous. If DeltaG gt 0 , the reaction is non-spontanous. If DeltaG=0 , the reaction is at equilibrium. In the equation, DeltaG=DeltaH-TDeltaS , temperature is a weighting factor that determine the relative importance of enthalpy contribution to DeltaG . Read the above paragraph carefully and answer the following questions based on above comprehension: One mole of ice is converted to liquid at 273 K, H_(2)O(s) and H_(2)O(l) have entropies 38.20 and 60.03 J "mol"^(-1) K^(-1) . Enthalpy change in the conversion will be:

Free energy, G=H-TS, is a state function that includes whether a reaction is spontaneous or non-spontaneous. If you think of TS as the part of the system's energy that is disordered already, then (H-TS) is the part of the system's energy that is still ordered and therefore free to cause spontaneous change by becoming disordered. Also, DeltaG=DeltaH-TDeltaS To see what this equation for free energy change has to do with spontaneity let us return to relationship. DeltaS_("total")=DeltaS_("sys")+DeltaS_("surr") = DeltaS + DeltaS_("surr") (It is generally understood that symbols without subscript refer to the system not the surroundings.) DeltaS_("surr")=-(DeltaH)/T , where DeltaH is the heat gained by then system at constant pressure. DeltaS_("total") = DeltaS -(DeltaH)/T rArr TDeltaH_("total")=DeltaH-TDeltaS rArr -TDeltaS_("total") =DeltaH-TDeltaS i.e. DeltaG=-TDeltaS_("total") From second law of thermodynamics, a reaction is spontaneous if DeltaS_("total") is positive, non-spontanous if DeltaS_("total") is negative and at equilibrium if DeltaS_("total") is zero. Since, -TDeltaS=DeltaG and since DeltaG and DeltaS have opposite signs, we can restate the thermodynamic criterion for the spontaneity of a reaction carried out at constant temperature and pressure. If DeltaG lt 0 , the reaction is spontaneous. If DeltaG gt 0 , the reaction is non-spontanous. If DeltaG=0 , the reaction is at equilibrium. In the equation, DeltaG=DeltaH-TDeltaS , temperature is a weighting factor that determine the relative importance of enthalpy contribution to DeltaG . Read the above paragraph carefully and answer the following questions based on above comprehension: A particular reaction has a negative value for the free energy change. Then at ordinary temperature.

Free energy, G=H-TS, is a state function that includes whether a reaction is spontaneous or non-spontaneous. If you think of TS as the part of the system's energy that is disordered already, then (H-TS) is the part of the system's energy that is still ordered and therefore free to cause spontaneous change by becoming disordered. Also, DeltaG=DeltaH-TDeltaS To see what this equation for free energy change has to do with spontaneity let us return to relationship. DeltaS_("total")=DeltaS_("sys")+DeltaS_("surr") = DeltaS + DeltaS_("surr") (It is generally understood that symbols without subscript refer to the system not the surroundings.) DeltaS_("surr")=-(DeltaH)/T , where DeltaH is the heat gained by then system at constant pressure. DeltaS_("total") = DeltaS -(DeltaH)/T rArr TDeltaH_("total")=DeltaH-TDeltaS rArr -TDeltaS_("total") =DeltaH-TDeltaS i.e. DeltaG=-TDeltaS_("total") From second law of thermodynamics, a reaction is spontaneous if DeltaS_("total") is positive, non-spontanous if DeltaS_("total") is negative and at equilibrium if DeltaS_("total") is zero. Since, -TDeltaS=DeltaG and since DeltaG and DeltaS have opposite signs, we can restate the thermodynamic criterion for the spontaneity of a reaction carried out at constant temperature and pressure. If DeltaG lt 0 , the reaction is spontaneous. If DeltaG gt 0 , the reaction is non-spontanous. If DeltaG=0 , the reaction is at equilibrium. In the equation, DeltaG=DeltaH-TDeltaS , temperature is a weighting factor that determine the relative importance of enthalpy contribution to DeltaG . Read the above paragraph carefully and answer the following questions based on above comprehension: Which of the following is true for the reaction? H_(2)O(l) H_(2)O(g) at 100^(@) C and 1 atmosphere?

Free energy, G=H-TS, is a state function that includes whether a reaction is spontaneous or non-spontaneous. If you think of TS as the part of the system's energy that is disordered already, then (H-TS) is the part of the system's energy that is still ordered and therefore free to cause spontaneous change by becoming disordered. Also, DeltaG=DeltaH-TDeltaS To see what this equation for free energy change has to do with spontaneity let us return to relationship. DeltaS_("total")=DeltaS_("sys")+DeltaS_("surr") = DeltaS + DeltaS_("surr") (It is generally understood that symbols without subscript refer to the system not the surroundings.) DeltaS_("surr")=-(DeltaH)/T , where DeltaH is the heat gained by then system at constant pressure. DeltaS_("total") = DeltaS -(DeltaH)/T rArr TDeltaH_("total")=DeltaH-TDeltaS rArr -TDeltaS_("total") =DeltaH-TDeltaS i.e. DeltaG=-TDeltaS_("total") From second law of thermodynamics, a reaction is spontaneous if DeltaS_("total") is positive, non-spontanous if DeltaS_("total") is negative and at equilibrium if DeltaS_("total") is zero. Since, -TDeltaS=DeltaG and since DeltaG and DeltaS have opposite signs, we can restate the thermodynamic criterion for the spontaneity of a reaction carried out at constant temperature and pressure. If DeltaG lt 0 , the reaction is spontaneous. If DeltaG gt 0 , the reaction is non-spontanous. If DeltaG=0 , the reaction is at equilibrium. In the equation, DeltaG=DeltaH-TDeltaS , temperature is a weighting factor that determine the relative importance of enthalpy contribution to DeltaG . Read the above paragraph carefully and answer the following questions based on above comprehension: For the spontaneity of a reaction, which statement is true?

Free energy, G=H-TS, is a state function that includes whether a reaction is spontaneous or non-spontaneous. If you think of TS as the part of the system's energy that is disordered already, then (H-TS) is the part of the system's energy that is still ordered and therefore free to cause spontaneous change by becoming disordered. Also, DeltaG=DeltaH-TDeltaS To see what this equation for free energy change has to do with spontaneity let us return to relationship. DeltaS_("total")=DeltaS_("sys")+DeltaS_("surr") = DeltaS + DeltaS_("surr") (It is generally understood that symbols without subscript refer to the system not the surroundings.) DeltaS_("surr")=-(DeltaH)/T , where DeltaH is the heat gained by then system at constant pressure. DeltaS_("total") = DeltaS -(DeltaH)/T rArr TDeltaH_("total")=DeltaH-TDeltaS rArr -TDeltaS_("total") =DeltaH-TDeltaS i.e. DeltaG=-TDeltaS_("total") From second law of thermodynamics, a reaction is spontaneous if DeltaS_("total") is positive, non-spontanous if DeltaS_("total") is negative and at equilibrium if DeltaS_("total") is zero. Since, -TDeltaS=DeltaG and since DeltaG and DeltaS have opposite signs, we can restate the thermodynamic criterion for the spontaneity of a reaction carried out at constant temperature and pressure. If DeltaG lt 0 , the reaction is spontaneous. If DeltaG gt 0 , the reaction is non-spontanous. If DeltaG=0 , the reaction is at equilibrium. In the equation, DeltaG=DeltaH-TDeltaS , temperature is a weighting factor that determine the relative importance of enthalpy contribution to DeltaG . Read the above paragraph carefully and answer the following questions based on above comprehension: If an endothermic reaction is non-spontaneous at freezing point of water and becomes feasible at its boiling point, then

Assertion : The difference between DeltaH and DeltaU is not significant for systems consisting of only solids and/or liquids. Reason : Solids and liquids do not suffer any significant volume changes upon heating.

A vessel contains 1 mole of O_(2) gas (molar mass 32 ) at a temperature T . The pressure of the gas is P . An identical vessel containing one mole of He gas (molar mass 4 ) at a temperature 2T has a pressure of xP . Find the value of x.

DeltaU^@ of combustion of methane is -X kJ mol^(-1) . The value of DeltaH^@ is

VMC MODULES ENGLISH-THERMOCHEMISTRY-JEE MAIN (ARCHIVE)
  1. For the reaction, C+O(2) rarr CO(2),DeltaH=-393 J 2Zn + O(2) rarr...

    Text Solution

    |

  2. The heats of combustion of carbon and carbon monoxide are -393.5 and ...

    Text Solution

    |

  3. The standard enthalpy of formation (Delta(f)H^(@)) at 298K for methan...

    Text Solution

    |

  4. The enthaplpy changes state for the following processes are listed bel...

    Text Solution

    |

  5. Standard entropies of X(2), Y(2) and XY(3) are 60, 40 and 50 JK^(–1) m...

    Text Solution

    |

  6. In a fuel cell methanol is used as fuel and oxygen gas is used as an o...

    Text Solution

    |

  7. On the basis of the following thermochemical data : (Delta(f)G^(@)H((a...

    Text Solution

    |

  8. The standard enthalpy of formation of NH3 is -46.0 kJ mol^(-1). If the...

    Text Solution

    |

  9. The value of enthalpy change (DeltaH) for the reaction C2H5OH(l) + 3...

    Text Solution

    |

  10. Consider the reaction, 4NO(2)(g)+O(2)(g)rarr2N(2)O(5)(g),Delta(r )H=...

    Text Solution

    |

  11. For complete combustion of ethanol, C(2)H(5)OH(l) + 3O(2)(g) rarr 2CO(...

    Text Solution

    |

  12. The combustion of benzene(/) gives CO2(g) and H2O(l) Given that heat o...

    Text Solution

    |

  13. For which of the following reactions, DeltaH is equal to DeltaU ?

    Text Solution

    |

  14. Given (i) 2Fe(2)O(3)(s) rarr 4Fe(s)+3O(2)(g), DeltaG^(@)=+1487.0 ...

    Text Solution

    |

  15. For which of the following processes is DeltaS negative?

    Text Solution

    |

  16. Given C(("graphite"))+O(2)(g)toCO(2)(g), Delta(r)H^(0)=-393.5kJ" "mo...

    Text Solution

    |

  17. The difference between DeltaH and DeltaU (DeltaH - DeltaU), when th...

    Text Solution

    |

  18. Enthalpy of sublimation of iodine is "24 cal g"^(-1)" at " 200^(@)C. ...

    Text Solution

    |

  19. The standard heat of formation (Delta(f)H(298)^(0)) of ethane (in kJ/m...

    Text Solution

    |

  20. If enthalpy of atomisatio for Br((2(l))) is xKJ//mol, the relation bet...

    Text Solution

    |