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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

a.4

B

b.6

C

c.1

D

d.NONE OF THE ABOVE

Text Solution

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The correct Answer is:
To solve the problem, we need to find the difference between the enthalpy change (ΔH) and the internal energy change (ΔU) during the combustion of one mole of heptane (C7H16) at a temperature T. We will use the relationship between ΔH and ΔU, which is given by the equation: \[ \Delta H = \Delta U + \Delta n_g RT \] where Δn_g is the change in the number of moles of gas during the reaction, R is the gas constant, and T is the temperature. ### Step-by-Step Solution: 1. **Write the balanced combustion reaction of heptane:** The combustion of heptane can be represented as: \[ C_7H_{16(l)} + 11 O_{2(g)} \rightarrow 7 CO_{2(g)} + 8 H_2O_{(l)} \] 2. **Identify the number of moles of gaseous reactants and products:** - **Reactants:** 11 moles of \(O_2\) (gaseous) - **Products:** 7 moles of \(CO_2\) (gaseous) The water produced is in liquid form, so it does not contribute to Δn_g. 3. **Calculate Δn_g:** \[ \Delta n_g = \text{(moles of gaseous products)} - \text{(moles of gaseous reactants)} = 7 - 11 = -4 \] 4. **Substitute Δn_g into the equation for ΔH:** Now, we can substitute Δn_g into the equation: \[ \Delta H = \Delta U + (-4)RT \] Rearranging gives: \[ \Delta H - \Delta U = -4RT \] 5. **Identify the value of x:** According to the problem, we have: \[ \Delta H - \Delta U = -xRT \] Comparing both equations, we find that: \[ -xRT = -4RT \] Thus, \(x = 4\). ### Final Answer: The value of \(x\) is **4**. ---

To solve the problem, we need to find the difference between the enthalpy change (ΔH) and the internal energy change (ΔU) during the combustion of one mole of heptane (C7H16) at a temperature T. We will use the relationship between ΔH and ΔU, which is given by the equation: \[ \Delta H = \Delta U + \Delta n_g RT \] where Δn_g is the change in the number of moles of gas during the reaction, R is the gas constant, and T is the temperature. ...
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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

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