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(A) For adsorption DeltaG, DeltaS, and D...

(A) For adsorption `DeltaG`, `DeltaS`, and `DeltaH` all have negative value.
(R) Adsorption is a spontanous process accompained by decrease in randomness.

A

If both (A) and (R) are true and (R) is the correct explanation of (A).

B

If both (A) and (R) are true but (R) is not the correct explanation of (A).

C

If (A) is correct but (R) is incorrect.

D

If (A) and (R) are both incorrect.

Text Solution

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The correct Answer is:
A
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Assertion : For adsorption DeltaG, DeltaH, DeltaS all have –ve values Reason : Adsorption is a spontaneous exothermic process in which randomness decreases due to force of attraction between adsorbent and adsorbate.

Assertion : During adsorption, DeltaG, DeltaH and DeltaS decrease i.e., their values become negative. Reason : Adsorption is a spontaneous process. Randomness ofr disorder decreases during adsorption.

each question constain STATEMENT-1(Assertion ) and STATEMENT - 2 (reason). examine the statement carefully and work the correct answer accoridng to the instructions given below : STATEMEN1: For Adsorption DeltaG,DeltaH,DeltaS all have -ve values. STATEMENT-2: Adsoption is a exothermic process in which randomness decreases due to force of attraction between adsorbent and adsorbate.

When Delta H and TDeltaS both are negative , then for spontaneous process which option is true?

The adsorption of vapours on a clean surface is a spontaneous process because

Which of the following is true during adsorption? a. DeltaG , DeltaH , and DeltaS all are negative. b. DeltaG is negative, but DeltaH and DeltaS is positive. c. DeltaG and DeltaH are negative, but DeltaS is positive. d. DeltaG and DeltaS are negative, but DeltaH is positive.

For a process top be spontaneous, at constant temperature and pressure, there must be decreases in free energy of the system in the direction of the process, i.e. DeltaG_(P.T.)lt0.Delta_(P.T.)=0 implies the equilibrium condition and DeltaG_(P.T.)gt0 corresponding to non-spontaneity. Gibb's Helmholtz equation relates the free energy change to the enthalpy and entropy change of the process as : DeltaG_(P.T.)=DeltaH-TDeltaS ......(i) The magnitude of Delta H does not change much with the change in temperature but the entropy factor TDeltaS changes appreciably. Thus, spontaneity of a process depends very much on temperature. For edothermic proces, both DeltaH "and " DeltaS are positive. The energy factor,the first factor of equation, opposes the spontaneity whereas entropy factor favours it . At low temperature, the favourable factor TDeltaS will be small and may be less than Delta H, DeltaG will have positive value indicating the non-spontaneity of the process. On raising temperature, the factor TDeltaS increases appreciably and when it exceeds DeltaH,DeltaG would become negative and the process would be spontaneous. For an exothermic process, both DeltaH " and " DeltaS would be negative. In this case, the first factor of equation(i) favours the spontaneity whereas the second factor opposes it. At high temperature, when TDeltaSgt DeltaH, DeltaG will have positive value, showing thereby the non-spontaneity of the process. However, on decreasing temperature, the factore TDeltaSlt DeltaH,DeltaG becomes negative and the process occurs spontaneously. Thus, an exothermic process may be spontaneous at low temperature and non-spontaneous at high temperature. A reaction has a value of DeltaH =-40 kcal at 400K . Above 400K, the reaction is spontaneous, below this temperature, it is not. The value of DeltaG " and "DeltaS at 400K are respectively:

For a process top be spontaneous, at constant temperature and pressure, there must be decreases in free energy of the system in the direction of the process, i.e. DeltaG_(P.T.)lt0.Delta_(P.T.)=0 implies the equilibrium condition and DeltaG_(P.T.)gt0 corresponding to non-spontaneity. Gibb's Helmholtz equation relates the free energy change to the enthalpy and entropy change of the process as : DeltaG_(P.T.)=DeltaH-TDeltaS ......(i) The magnitude of Delta H does not change much with the change in temperature but the entropy factor TDeltaS changes appreciably. Thus, spontaneity of a process depends very much on temperature. For edothermic proces, both DeltaH "and " DeltaS are positive. The energy factor,the first factor of equation, opposes the spontaneity whereas entropy factor favours it . At low temperature, the favourable factor TDeltaS will be small and may be less than Delta H, DeltaG will have positive value indicating the non-spontaneity of the process. On raising temperature, the factor TDeltaS increases appreciably and when it exceeds DeltaH,DeltaG would become negative and the process would be spontaneous. For an exothermic process, both DeltaH " and " DeltaS would be negative. In this case, the first factor of equation(i) favours the spontaneity whereas the second factor opposes it. At high temperature, when TDeltaSgt DeltaH, DeltaG will have positive value, showing thereby the non-spontaneity of the process. However, on decreasing temperature, the factore TDeltaSlt DeltaH,DeltaG becomes negative and the process occurs spontaneously. Thus, an exothermic process may be spontaneous at low temperature and non-spontaneous at high temperature. For the reaction at 298K, 2A+B toC" " Delta H =100 kcal and DeltaS= 0.050 kcal K^(-1) . If DeltaH " and " DeltaS are assumed to be constant over the temperature range, just above what temperature will be reaction become spontaneous?

For a process top be spontaneous, at constant temperature and pressure, there must be decreases in free energy of the system in the direction of the process, i.e. DeltaG_(P.T.)lt0.Delta_(P.T.)=0 implies the equilibrium condition and DeltaG_(P.T.)gt0 corresponding to non-spontaneity. Gibb's Helmholtz equation relates the free energy change to the enthalpy and entropy change of the process as : DeltaG_(P.T.)=DeltaH-TDeltaS ......(i) The magnitude of Delta H does not change much with the change in temperature but the entropy factor TDeltaS changes appreciably. Thus, spontaneity of a process depends very much on temperature. For edothermic proces, both DeltaH "and " DeltaS are positive. The energy factor,the first factor of equation, opposes the spontaneity whereas entropy factor favours it . At low temperature, the favourable factor TDeltaS will be small and may be less than Delta H, DeltaG will have positive value indicating the non-spontaneity of the process. On raising temperature, the factor TDeltaS increases appreciably and when it exceeds DeltaH,DeltaG would become negative and the process would be spontaneous. For an exothermic process, both DeltaH " and " DeltaS would be negative. In this case, the first factor of equation(i) favours the spontaneity whereas the second factor opposes it. At high temperature, when TDeltaSgt DeltaH, DeltaG will have positive value, showing thereby the non-spontaneity of the process. However, on decreasing temperature, the factore TDeltaSlt DeltaH,DeltaG becomes negative and the process occurs spontaneously. Thus, an exothermic process may be spontaneous at low temperature and non-spontaneous at high temperature. The enthalpy change for a certain reaction at 300K is -15.0 k cal mol^(-1) . The entropy change under these conditions is -7.2 cal K^(-1) mol ^(-1) . The free energy change for the reaction and its spontaneous/non-spontaneous character will be :

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