Home
Class 12
CHEMISTRY
DeltaU^(@) of combustoin of methane is -...

`DeltaU^(@)` of combustoin of methane is `-XKJ mol ^(-1)` The value
of `DeltaH^(@)` is :-

A

`-X-596R`

B

`-X+596R`

C

`X+596R`

D

`X-596R`

Text Solution

AI Generated Solution

The correct Answer is:
To find the standard enthalpy change (ΔH°) for the combustion of methane given the standard internal energy change (ΔU°) is -X kJ/mol, we can follow these steps: ### Step 1: Understand the relationship between ΔH° and ΔU° The relationship between the standard enthalpy change (ΔH°) and the standard internal energy change (ΔU°) is given by the equation: \[ \Delta H^\circ = \Delta U^\circ + \Delta N_g R T \] where: - ΔN_g = change in the number of moles of gas - R = universal gas constant (8.314 J/(mol·K)) - T = temperature in Kelvin (298 K for standard conditions) ### Step 2: Write the combustion reaction of methane The balanced chemical equation for the combustion of methane (CH₄) is: \[ \text{CH}_4(g) + 2\text{O}_2(g) \rightarrow \text{CO}_2(g) + 2\text{H}_2\text{O}(l) \] ### Step 3: Calculate ΔN_g ΔN_g is calculated as: \[ \Delta N_g = \text{moles of gaseous products} - \text{moles of gaseous reactants} \] From the reaction: - Moles of gaseous products = 1 (from CO₂) - Moles of gaseous reactants = 1 (from CH₄) + 2 (from O₂) = 3 Thus, \[ \Delta N_g = 1 - 3 = -2 \] ### Step 4: Substitute values into the equation Now we can substitute ΔU°, ΔN_g, R, and T into the equation: \[ \Delta H^\circ = \Delta U^\circ + \Delta N_g R T \] Substituting the known values: \[ \Delta H^\circ = -X + (-2)(8.314 \, \text{J/(mol·K)})(298 \, \text{K}) \] ### Step 5: Convert R to kJ Since ΔU° is given in kJ, we need to convert R from J to kJ: \[ R = 8.314 \, \text{J/(mol·K)} = 0.008314 \, \text{kJ/(mol·K)} \] ### Step 6: Calculate ΔH° Now substituting R in kJ: \[ \Delta H^\circ = -X - 2(0.008314)(298) \] Calculating the second term: \[ \Delta H^\circ = -X - 4.964 \, \text{kJ} \] ### Final Answer Thus, the final expression for ΔH° is: \[ \Delta H^\circ = -X - 4.964 \, \text{kJ/mol} \]

To find the standard enthalpy change (ΔH°) for the combustion of methane given the standard internal energy change (ΔU°) is -X kJ/mol, we can follow these steps: ### Step 1: Understand the relationship between ΔH° and ΔU° The relationship between the standard enthalpy change (ΔH°) and the standard internal energy change (ΔU°) is given by the equation: \[ \Delta H^\circ = \Delta U^\circ + \Delta N_g R T \] where: ...
Promotional Banner

Topper's Solved these Questions

  • CHEMISTRY AT A GLANCE

    ALLEN|Exercise INORGANIC CHEMISTRY|300 Videos
  • CHEMISTRY AT A GLANCE

    ALLEN|Exercise ORGANIC CHEMISTRY|472 Videos
  • Chemical Equilibrium

    ALLEN|Exercise All Questions|30 Videos
  • ELECTROCHEMISTRY

    ALLEN|Exercise EXERCISE -05 [B]|38 Videos

Similar Questions

Explore conceptually related problems

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

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

Change in enthalpy and change in internal energy are state functions. The value of DeltaH, DeltaU can be determined by using Kirchoff's equation. Calculate the heat of formation of methane, given that heat of formation of water = -286kJ mol^(-1) , heat of combustion of methane = -890kJ mol^(-1) heat of combustion of carbon = -393.5 kJ mol^(-1)

The value of DeltaH^(@) for the reaction Cu^(+)(g)+I^(-)(g)toCuI(g) is -446kJ mol^(-1) . If the ionisation energy of Cu(g) is 745 kJ mol^(-1) and the electron affinity of I(g) is -295 kJ mol^(-1) , then the value of DeltaH^(@) for the formation of one mole of CuI(g) from Cu(g) and I(g) is:

The DeltaH_(f)^(0)(KF,s) is -563 kJ mol^(-1) . The ionization enthalpy of K(g) is 419 kJ mol^(-1) . and the enthalpy of sublimation of potassium is 88 kJ mol^(-1) . The electron affinity of F(g) is 322 kJ mol^(-1) and F-F bond enthalpy is 158 kJ mol^(_1) . Calculate the lattice enthalpy of KF(s) . The given data are as follows: (i) K(s)+1//2F_(2)(g)rarrKF(s)" "DeltaH_(f)^(0)= -563 kJ mol^(-1) (ii) K(g)rarrK^(+)(g)+e^(-)" "Delta_("Ioniz")^(0)=419 kJ mol^(-1) (iii) K(s)rarrK(g)" "DeltaH_("sub")^(0)=88kJ mol^(-1) (iv) F(g)+e^(-)rarrF^(-)(g)" "DeltaH_(eg)^(0)= -322 kJ mol^(-1) (v) F_(2)(g)rarr2F(s)" "DeltaH_("diss")^(0)= 158 kJ mol^(-1) (vi) K^(+)(g)+F^(-)(g)rarrKF(s)" " DeltaH_(L)^(0)=?

The first (DeltaH_(1)) and second (DeltaH_(2)) ionisation enthalpies (in kJ mol^(-1)) and the (DeltaH_(eg)) electron gain enthalpy (in kJ mol^(-1)) of a elements are given below: Based on the above information match the following columns.

For a gaseous reaction, A(g)+3B(g)to3C(g)+3D(g),DeltaU is 17 kcal at 27^(@)C . Assuming R=2cal" "K^(-1)mol^(-1) , the value of DeltaH for the above reaction is:

Given C_(2)H_(2)(g)+H_(2)(g)rarrC_(2)H_(4)(g): DeltaH^(@)=-175 " kJ mol"^(-1) DeltaH_(f(C_(2)H_(4),g))^(@)=50 " kJ mol"^(-1), DeltaH_(f(H_(2)O,l))^(@)=-280 " kJ mol"^(-1), DeltaH_(f(CO_(2)g))^(@)=-390 " kJ mol"^(-1) If DeltaH^(@) is enthalpy of combustion (in kJ "mol"^(-1) ) of C_(2)H_(2) (g), then calculate the value of |(DeltaH^(@))/(257)|

Calculate the heat of formation of methane in kcalmol^(-1) using the following thermo chemical reactions C(s)+O_(2)toCO_(2)(g) , DeltaH=-94.2 kcal mol^(-1) H_(2)(g)+1/2O_(2)(g)toH_(2)O(l) , DeltaH=-68.3 kcal mol^(-1) CH_(4)(g)+2O_(2)(g)toCO_(2)(g)+2H_(2)O(l) , DeltaH=-210.8 kcal mol^(-1)

Standard enthalpy of vapourisation DeltaH^(@) forwater is 40.66 KJ mol^(-1) .The internal energy of vapourisation of water for its 2 mol will be :-