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प्रश्न
Represent the potential energy/enthalpy change in the following processes graphically.
(a) Throwing a stone from the ground to roof.
(b) \[\ce{1/2 H2(g) + 1/2 Cl2 (g) ⇌ HCl (g) Δ_rH^Θ = - 92.32 kJ mol^{-1}}\]
In which of the processes potential energy/enthalpy change is contributing factor to the spontaneity?
उत्तर
(a) Throwing a stone from ground to roof
(b) The reaction involved is a process where the energy decreases after the reaction. It can be represented as:
In process (b), potential energy/enthalpy change is a contributing factor to the spontaneity.
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संबंधित प्रश्न
For an ideal gas, the work of reversible expansion under isothermal condition can be calculated by using the expression w = `- nRT` In `V_f/V_i`. A sample containing 1.0 mol of an ideal gas is expanded isothermally and reversibly to ten times of its original volume, in two separate experiments. The expansion is carried out at 300 K and at 600 K respectively.
(i) Work done at 600 K is 20 times the work done at 300 K.
(ii) Work done at 300 K is twice the work done at 600 K.
(iii) Work done at 600 K is twice the work done at 300 K.
(iv) ∆U = 0 in both cases.
A sample of 1.0 mol of a monoatomic ideal gas is taken through a cyclic process of expansion and compression as shown in figure 6.1. What will be the value of ∆H for the cycle as a whole?
Expansion of a gas in vacuum is called free expansion. Calculate the work done and the change in internal energy when 1 litre of ideal gas expands isothermally into vacuum until its total volume is 5 litre?
What will be the work done on an ideal gas enclosed in a cylinder, when it is compressed by a constant external pressure, pext in a single step as shown in figure. Explain graphically.
An ideal gas is allowed to expand against a constant pressure of 2 bar from 10 L to 50 L in one step. Calculate the amount of work done by the gas. If the same expansion were carried out reversibly, will the work done be higher or lower than the earlier case? (Given that 1 L bar = 100 J)
Match the following :
A | B |
(i) Adiabatic process | (a) Heat |
(ii) Isolated system | (b) At constant volume |
(iii) Isothermal change | (c) First law of thermodynamics |
(iv) Path function | (d) No exchange of energy and matter |
(v) State function | (e) No transfer of heat |
(vi) ΔU = q | (f) Constant temperature |
(vii) Law of conservation of energy | (g) Internal energy |
(viii) Reversible process | (h) Pext = o |
(ix) Free expansion | (i) At constant pressure |
(x) ΔH = q | (j) Infinitely slow process which proceeds through a series of equilibrium states. |
(xi) Intensive property | (k) Entropy |
(xii) Extensive property | (l) Pressure |
(m) Specific heat |
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