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1701.

Consider the following reactions: `C(s)+O_(2)(g)toCO_(2)(g)+x " kJ"` `CO(g)+(1)/(2)O_(2)(g)toCO_(2)(g)+y" kJ"` The heat formation of CO(g) is :A. `-(x+y)` kJ/molB. `(x-y)` kJ/molC. `(y-x)` kJ/molD. None of these

Answer» Correct Answer - C
`C(s)+O_(2)(g)rarrCO_(2)(g),`
`Delta_(r )H_(1)=-x" kJ"//"mol .....(1)"`
`CO(g)+1//2O_(2)(g)rarrCO_(2)(g)`
`Delta_(r ) H_(2)=-y " kJ"//"mol .....(2)"`
Equation (1) - (2)
`C(s)+(1)/(2)O_(2)(g)rarrCO(g)`
`Delta_(f)H=(y-x)" kJ"//"mol"`
1702.

The reversible expansion of an ideal gas under adiabatic and isothermal conditions is shown in the figure. Which of the following statement(s) is (are) correct? A. `T_(1)=T_(2)`B. `T_(3)gtT_(1)`C. `w_("isothermal")gtw_("adiabatic")`D. `DeltaU_("isothermal")gtDeltaU_("adiabatic")`

Answer» Correct Answer - A::D
For isothermal expansion, `DeltaT=`constant i.e. `T_(1)=T_(2)`
at const temperature, internal energy `(DeltaU)` of the system remains constant i.e.,
`DeltaU_("isothermal")=0`
Reversible expansion work=`-2.303nRT"log"(V_(2))/(V_(1))`
In adiabatic expansion, no heat is allowed to enter `w` is leave the system, hence `q = 0`
`DeltaE=q+w. :. q = 0`
`DeltaE=w`
In expansion, work is doen by the system, hence `w` is negative, accordingly, `DeltaE=-ve`, i.e.,
Internal energy decrease and therefore the temperature of the system falls.
Thus, `T_(3) lt T_(1)`
Thus, `DeltaU_("adiabatic")=-ve`
Thus, `DeltaU_("Isothermal") gt DeltaU_("adiabatic")`
`w_("adiabatic")=R/((gamma-1))(T_(2)-T_(1))`
Thus, Including sign,
`w_("isothermal") lt w_("adiabatic")`
1703.

State the thermodynamic conditions of spontaneous occurence of a process.

Answer» For spontaneous occurrence,`DeltaG` of the process mustbe `( lt 0 , i.e., -ve`. .This can be so under the following conditions `:` (i) `DeltaH ` is negative and`DeltaS` is positive( at any temperature).
(ii) If `DeltaH` and`DeltaS` both are positive , then T should be so high that`TDelta S gt Delta H`.
(iii) If both `Delta H ` and`DeltaS` are negative, then T should be solow that `T Delta lt DeltaH `
1704.

If `Delta_(f)H^(@)(C_(2)H_(4))` and `Delta_(f)H^(@)(C_(2)H_(6))` are `x_(1)` and `x_(2)` kcal `mol^(-1)`, then heat of hydrogenation of `C_(2)H_(4)` is :A. `x_(1)+x_(2)`B. `x_(1)-x_(2)`C. `x_(2)-x_(1)`D. `x_(1)+2x_(2)`

Answer» Correct Answer - C
1705.

Assertion (A): The thermodynamic factor which determines the spontaneity of a process is the free energy. For a process to be spontaneous the free energy must be-ve. Reason (R ) : The change in free energy is related to the change in a process must always be positive if its is spontaneous.A. If both (A) and (R ) are correct, and (R ) is the correct explanation for (A).B. If the both (A) and (R ) are correct, but(R ) is not a correct explanation for (A).C. If (A) is correct, but (R ) is incorrect.D. If (A) is incorrect, but (R ) is correct.

Answer» For a spontaneous process, `DeltaG` must be negative.
1706.

Which of the following thermodynamic condition at constant pressure and temperature is necessary for the spontaneity of a process?A. `d(E-TS+PV) gt0`B. `d(E-TS+PV) lt0`C. `d(E-TS+PV) =0`D. `d(E+TS+PV) lt 0`

Answer» Correct Answer - B
1707.

The bond dissociation energies of gaseous `H_(2),C1_(2)`, and `HC1` are `100, 50`, and `100 kcal mol^(-1)`, respectively. Calculate the enthalpy of formation of `HC1(g)`.

Answer» The required equation is
`(1)/(2)H_(2)(g) +(1)/(2)C1_(2)(g) rarr HC1(g), DeltaH^(Theta) = ?`
`DeltaH^(Theta) =[(1)/(2)DeltaH_(H-H) +(1)/(2)DeltaH_(C1-C1)] =[DeltaH_(H-CI)^(Theta)]`
`= (1)/(2) xx 100 +(1)/(2) xx 50 - 100`
`=- 25 kcal mol^(-1)`
1708.

Which of the following are not state functions? (I) `q+w` (II)`q` (III) `w` (IV) `H-TS`A. (I),(II) and (III)B. (II) and (III)C. (I) and (IV)D. (II), (III) and (IV)

Answer» Correct Answer - B
1709.

Find the work done by the gas in the process `ABC`. A. `3/2 P_(0)V_(0)`B. `5/2P_(0)V_(0)`C. `7/2 P_(0)V_(0)`D. `4P_(0)V_(0)`

Answer» Correct Answer - C
1710.

Assertion : The entropy of the solids is the highest Reason : Atoms of the solids are arranged in orderly manner.A. If both assertion and reason are true and the reason is the correct explanation of the assertion.B. If both assertion and reason are true but reason is not the correct explanation of t he assertion.C. If assertion is true but reason is false.D. If the assertion and reason both are false

Answer» Correct Answer - A
1711.

Assertion : Efficiency of a Carnot engine increase on reducing the temperature of sink. Reason : The efficiency of a Carnot engine is defined as ratio of net mechanical work done per cycle by the gas to the amount of heat energy absorbed per cycle from the source.A. If both assertion and reason are true and the reason is the correct explanation of the assertion.B. If both assertion and reason are true but reason is not the correct explanation of t he assertion.C. If assertion is true but reason is false.D. If the assertion and reason both are false

Answer» Correct Answer - B
1712.

If for hydrogen `C_(P) - C_(V) = m` and for nitrogen `C_(P) - C_(V) = n`, where `C_(P)` and `C_(V)` refer to specific heats per unit mass respectively at constant pressure and constant volume, the relation between `m` and `n` is (molecular weight of hydrogen = 2 and molecular weight or nitrogen = 14)A. `n=14m`B. `n=7m`C. `m=7n`D. `m=14n`

Answer» Correct Answer - D
`C_(P)-C_(V)=mM("for", H_(2)),C_(P)-C_(V)=nM("for" , N_(2))`
1713.

Two moles of an ideal gas undergoes Isothermal expansion when heat is supplied to It. If the gas is at room temperature (298K) and the final volume is thrice the Initial volume, find the total heat supplied.

Answer»

No of moles, n = 2

temperature, T = 298K

let initial volume = Vi

∴ final volume, Vf = 3Vi

The work done for isothermal process is given by,

W = 2.303 nRT log10 \((\frac{v_2}{v_1})\) 

where V2 is the final volume and V1 is the initial volume.

Here \(\frac{v_2}{v_1}\) = \(\frac{v_f}{v_i}\) = 3

∴ W = 2.303 × 2 × 8.314 × 298 × \({log^3_{10}}\)

W = 5.44kJ

Since, for isothermal process, Heat supplied is equal to work done by the gas, the total heat supplied is 5.44 kJ.

1714.

Give some examples of adiabatic process.

Answer»

(i) Sudden bursting of the tube of bicycle tyre. 

(ii) Propagation of sound waves in air and other gases.

1715.

Which one of the following statements about state funcitons is correct?A. Internal enegy enthalpy, heat and work are all thermodynamic state functions.B. A state function depends both on the past history of a system and on it present condition.C. The state function describing a system of equilibrium chnage with time.D. The difference in a state function for any process depends only on the intial and final states.

Answer» State functions does not depend upon the path of the process.
1716.

A quantity of an ideal gas at `17^(@)C` is compressed adiabatically to `1/8th of its initial volume. Calculate the final temp. if the gas in monoatomic.

Answer» Here, `T_(1)= 17^(@)C= 17+273= 290K`
`V_(2)= 1/8V_(1), T_(2)=?`
For monoatomic gas `gamma = 5//3`
As the process is adiabatic, therefore,
`T_(2)V_(2)^(gamma-1)=T_(1)V_(1)^(gamma-1)`
`T_(2)= T_(1)((V_(1))/(V_(2)))^(gamma-1)`
`= 290(8)^(5//3-1)=(290)xx(8)^(2//3)`
`= 290xx4= 1160K`
1717.

The rapid depletion of fossil fuels has inspired extensive research in the area of alternative and renewale energy sources. Of these, hydroden is the most Contemplated fuel of the future . Howevercost effective production and hazard free storage are major issuses is using `H_(2)` (Note : use the data in table-1 given at the end of partA, whenever necessary.) Assuming complete combustion, calculate heat of combustion when (i)1 g of hydrogen and (ii) 1 g of carbon are burnt.

Answer» Correct Answer - `i) DeltaH =- 143 KJ g^(-1)` of hydrogen
`ii) DeltaH=-32.8 KJ g^(-1)` of carbon
1718.

The rapid depletion of fossil fuels has inspired extensive research in the area of alternative and renewale energy sources. Of these, hydroden is the most Contemplated fuel of the future . Howevercost effective production and hazard free storage are major issuses is using `H_(2)` (Note : use the data in table-1 given at the end of partA, whenever necessary.) 1kg of hydrogen is burnt with oxgyen at `25^(@)C` and the heat energy is used for different purpose . Using this heat calculate (i) the maximum theoretical work. (ii) work that can be produced by a heat engine working between `25^(@)C` to `300^(@)` C. (The efficiency of a heat engine =work done /heat absorbed =`[1-9T_("low")//T_("high")]` where T is in K)

Answer» Correct Answer - (i) `DeltaG` is the max work`=-1.2 xx 10^(5)KJ`
(ii) Heat engine `=-6.9 xx 10^(4) KJ`
1719.

One method to produce hydrogen on an industrial on an industrial scale is the reaction of methane with overheated water vapour at 1100 K to form hydrogen and carbon monoxide . The reaction is known as steam reforming Write the balanced equations for the steam reforming of methane .

Answer» Correct Answer - `CH_(4)(g) + H_(2)O(g) rarr CO(g) + 3H_(2)(g)`
1720.

Given the enthalpy of formation of `CO_(2)(g)` is -94.0 KJ, of CaO(s) is -152 KJ, and the enthalpy of the reaction `CaCO_(3)(s) rarr CaO(s)+CO_(2)(g)` is 42KJ, the enthalpy of formation of `CaCO_(3) (s)` isA. `-42` KJB. `-202` KJC. `+202` KJD. `-288` KJ

Answer» Correct Answer - D
`CaCO_(3(s))rarr CaO_((s))+CO_(2(g)) , Delta H=42 kJ`
`Delta H=Sigma (Delta E_(f))_(P)-Sigma (Delta E_(f))_(R )`
`42=[-152)+(-94)]-Delta H_(f)(CaCO_(3))`
`therefore H_(f)(CaCO_(3))=-246-42 =-288 kJ`
1721.

For `CaCO_(3)(s)rarr CaO(s)+CO_(2)(g)` at `977^(@)C, Delta H = 174` KJ/mol , then `Delta E` is :-A. 160 KJB. 163.6 KJC. 186.4 KJD. 180 KJ

Answer» Correct Answer - B
1722.

The standard enthalpy of decomposition of the yellow complex `H_(3)NSO_(2)` into `NH_(3)` and `SO_(2)` is `+40 kJ mol^(-1)`. Calculate the standard enthalpy of formation of `H_(3)NSO_(3).DeltaH_(f)^(0)(NH_(3))= -46.17 kJ mol^(-1), DeltaH_(f)^(0)(SO)_(2)= -296.83`

Answer» Correct Answer - `-383 kJ mol^(-1)`
1723.

The dissociation pressure of `CaCO_(3)(s) overset(Delta) rarr CaO(s) +CO_(2)` gets doubled over a tempertaure range of `60` degree around the mean tempertaure of `837^(@)C`. Calculate the enthalpy of dissociation in kcal `mol^(-1)`.

Answer» `((T_(1)+T_(2)))/(2) = 837^(@)C`
`T_(1) -T_(2) = 60^(@)C`
`T_(1)T_(2) = 1140 xx1030`
Solve `T_(1) = 867^(@)C = 1140 K`
`T_(2) = 807^(@)C = 1080 K`
`"log"(K_(2))/(K_(1)) = "log"(P_(2))/(P_(1)) = (DeltaH)/(2.303R) [(60)/(1140 xx1080)]`
`log2 = (DeltaH)/(2.303 xx 2xx 10^(-3)) xx (60)/(1140 xx 1080)`
`DeltaH = 28.44 kcal mol^(-1)`
1724.

The state of a mole of an ideal gas changed from state `A` at pressure `2P` and volume `V` follows four different processes and finally returns to initial state `A` reversibly as shown below in the graph. By interpreting the graph, answer the following questions. what would the be total done by the gas?A. `-PV`B. `PV`C. `0`D. None of these

Answer» Work done `= - P DeltaV`
or `-P (2V -V) =- PV`
1725.

The state of a mole of an ideal gas changed from state `A` at pressure `2P` and volume `V` follows four different processes and finally returns to initial state `A` reversibly as shown below in the graph. By interpreting the graph, answer the following questions. What would be the work done in state `B to C`?A. `-PV`B. `PV`C. `2PV`D. Zero

Answer» In conversion from `B` to `C`, volume does not change or `DeltaV = 0`, therefore `w = 0`
1726.

The state of a mole of an ideal gas changed from state `A` at pressure `2P` and volume `V` follows four different processes and finally returns to initial state `A` reversibly as shown below in the graph. By interpreting the graph, answer the following questions. What would be the heat obsorbed by the system in this cyclic process?A. `-2PV`B. ZeroC. `2PV`D. `PV`

Answer» `q =- w`
`:. Q = PV`
1727.

The state of a mole of an ideal gas changed from state `A` at pressure `2P` and volume `V` follows four different processes and finally returns to initial state `A` reversibly as shown below in the graph. By interpreting the graph, answer the following questions. In state `D` to state `A`, what kind of process is followed?A. Isobaric expansionB. Isobaric compressionC. Isochoric processD. Isothermal compression

Answer» Expansion from state `D` to state `A` occurs at constant volume (isochoric process) `=V`
1728.

The state of a mole of an ideal gas changed from state `A` at pressure `2P` and volume `V` follows four different processes and finally returns to initial state `A` reversibly as shown below in the graph. By interpreting the graph, answer the following questions. Which is the kind of process followed from state `A` to state, `B`?A. Isochoric expansionB. Isobaric expansionC. Isothermal reversible expansionD. Isothermal irreversible compression

Answer» Expansion from state `A` to state `B` occurs at constant pressure (isobaric expansion ) `=2P`
1729.

When `12.0g` of carbon (graphite)reacted with oxygen to form `CO` and `CO_(2)` at `25^(@)C` and constant pressure, `252 kJ` of heat was released and no carbon remained. If `Delta H_(f)^(0)(CO,g)= -110.5 kJ mol^(-1)` and `Delta H_(f)^(0)(CO_(2),g)= -393.5 kJ mol^(-1)`,calculate the mass of oxygen consumed.

Answer» Correct Answer - `24 g`
We have
Amount of carbon `=(12.0g)/(12.0g mol^(-1))=1 mol`
The equation to be considered are
`C("graphite")=(1)/(2)O_(2)(g)rarrCO(g)DeltaH^(0)= -110.5 kJ mol^(-1)`
`C("graphite")+O_(2)(g)rarrCO_(2)(g)DeltaH^(0)= -393.5 kJ mol^(-1)`
Let the amount `x` of carbon be converted into `CO` and the remaining `(i.e. 1.0 mol-x)` into `CO_(2)`. we will have `[(x(-110.5)+(1.0 mol-x)(-393.5)]kJ mol^(-1) = -313.8 kJ`
Which gives `x=(252+393.5)/(393.5-110.5)mol=0.5 mol`
Amount of oxygen needed `=[(0.5)/(2)+(1.0-0.5)]mol=0.75 mol`
Mass of oxygen needed `=(0.75 mol)(32 g mol^(-1))=24 g`
1730.

When `12.0g` of `C` reacted with oxygen to form `CO` and `CO_(2)` at `25^(@)C` at constant pressure, `313.8 kJ` of heat was released and no carbon remained. Calculate the mass of oxygen which reacted. `Delta_(f)H^(Theta) (CO,g) =- 110.5 kJ mol^(-1)` and `Delta_(r)H^(Theta) (CO,g) =- 393.5 kJ mol^(-1)`

Answer» `{:(C + (1)/(2)O_(2) rarr CO ,,DeltaH =- 110.5),(C+O_(2)rarrCO_(2),,DeltaH =- 393.5):}`
Let `x mol` of `C` is converted into `CO` and `(1-x)` mol into `CO_(2)`.
`:.x (-110.5) +(1-x)(-393.5) =- 313.8`
`x = 0.2816 mol`
Amount of `O_(2)` needed `= (0.2816)/(2) +(1-0.2816)`
`= 0.8592 mol = 0.8592 xx 32`
`= 27.5 g`
1731.

When `12.0g` of `C` reacted with a limited quantity of oxygen, `57.5 kcal `of heat was produced. Calculate the number of `CO` and number of moles of `CO_(2)` produced. Given `C +O_(2) rarr CO_(2), Delta_(f)H = - 94.05 kcal` `C +1//2O_(2) rarr CO, Delta_(f)H =- 26.41 kcal `

Answer» `C = (12)/(12) = 1 mol`
`{:(C+,O_(2)rarr,CO_(2),DeltaH_(1)=-94.05kcal),(x,x,),(C+,(1)/(2)O_(2)rarr,CO,DeltaH_(2) =- 26.41 kcal),((1-x),,(1-x)):}`
`:.x (-94.05) +(1-x)(-26.41) =- 57.5`
`x = 0.46 mol of CO_(2)`
`1 -x = 0.54 mol of CO`
1732.

Calculate the standard enthalpy of formation of acetylene from the following data `:` `C_((g))+O_(2(g))rarr CO_(2(g)),DeltaH^(@)=-393kJ mol^(-1)` `H_(2(g))+(1)/(2)O_(2(g)) rarr H_(2)O_((l)),DeltaH^(@)=-285.8kJ mol^(-1)` `2C_(2)H_(2(g))+5O_(2(g))rarr 4CO_(2(g))+2H_(2)O_((l)),DeltaH^(@)=-2598.8kJ mol^(-1)`.

Answer» `{:(,Delta_(r )H^(@)),(4xx(a)4C("graphite")+4O_(2)(g)rarr4CO_(2)(g),bar(4(-393.5 kJ mol^(-1)))),(2xx(b)2H_(2)(g)+O_(2)rarr2H_(2)O(l),2(-285.8 kJ mol^(-1))),((-c)4CO_(2)(g)+2H_(2)O(l)rarr2C_(2)H_(2)(g)+5O_(2)(g)+,2598.8 kJ mol^(-1)):}/{:(4C("graphite")+2H_(2)(g)rarr2C_(2)H_(2)(g),Delta_(r )H^(@)=+453.2 kJ mol^(-1)),(or 2C("graphite")+H_(2)(g)rarrC_(2)H_(2)(g),Delta_(r )H^(@)=+226.6 kJ mol^(-1)):}`
Since the above thermochemical equation represents the synthesis of `C_(2)H_(2)` from its elements, we have `Delta_(r )H^(@)(C_(2)H_(2))=+226.6 kJ mol^(-1)`.
1733.

`Delta_(f)U^(c-)` of formation of `CH_(4)(g)` at certain temperature is`-393kJ mol^(-1)` . Thevalue of `Delta_(f)H^(c-)` isA. zeroB. ` lt Delta_(f)U^(c-)`C. `gt Delta_(f)U^(c-)`D. equalto `Delta_(f)U^(c-)`

Answer» Correct Answer - b
`CH_(4)(g) + 2O_(2)(g) rarr CO_(2)(g) + 2H_(2)O(l)`
`Deltan_(g) = ( n_(p)-n_(r))_(g)=1-3= -2`
`Delta_(f)H^(@) =Delta_(f)U^(@) + Deltan_(g) RT`
As `Deltan_(g) = - 2 , Delta_(f)H^(@) lt Delta_(f) U^(@)` .
1734.

Can a gas be liquefied at any temperature by the increase of pressure alone?

Answer»

A gas can be liquid by pressure alone, only when its temperature is below its critical temperature.

1735.

Can a gas be liquefied at any temperature by increase of pressure alone?

Answer»

No, a gas can be liquefied by pressure alone, only when temperature of gas is below its critical temperature.

1736.

State zeroth law of thermodynamics?

Answer»

Acc. to this, when the thermodynamic system A and B are separately in thermal equilibrium with a third thermodynamic system C, then the system A and B are in thermal equilibrium with each other also. 

1737.

Comment on the thermodynamic stability of NO(g), given 1/2N2(g) + 1/2O2(g) → NO(g); ΔrHθ = 90 kJ mol-1NO(g) + 1/2O2(g) → NO2(g); ΔgHθ = -74 kJ mol-1

Answer»

For NO(g); ΔrHθ = +ve : unstable in nature

For NO2(g); ΔrHθ = -ve : stable in nature.

1738.

The equilibrium constant for a reaction is 10. What will be the value of ΔG°? R = 8.314 JK-1 mol-1, T = 300 K

Answer»

ΔG° = -2.303 RT log Kc

= -2.303 x (8.314 mol-1 K-1) x 300 K log 10

= -2.303 x 8.314 x 300 x 1

= -5527 J mol-1

= -5.527 kJ mol-1

1739.

Justify the following statements : (a) Reaction with ΔG° < 0 always have an equilibrium constant greater than. (b) Many thermodynamically feasible reaction do not occur under ordinary conditions. (c) At low temperatures enthalpy change dominates the AG expression and at high temperature, it is the entropy which dominates the value of AG.

Answer»

(a) ΔG° = -2.303 RT logK If K > 1, ΔG° will be less than zero because products formed are more than that of reactants, i.e., process is spontaneous in forward direction. 

(b) It is because heat energy is required to overcome activation energy. 

(c) ΔG = ΔH - TΔS, At low temperatures ΔH > TΔS whereas at high temperature TΔS >ΔH 

∴ ΔG decreases, i.e., becomes negative.

1740.

Calculate the standard enthalpy of formation of CH3OH (l) from the following data:(i) CH3OH(l) + 3/2O2(g) → CO2(g) + 2H2O(l);ΔrH° = -726 kJ mol-1(ii) C(g) + O2(g) → CO2(g);ΔcH° = -393 kJ mol-1(iii) H2(g) + 1/2O2(g) → H2O(l);ΔfH° = -286 kJ mol-1

Answer»

(i) CH3OH(l) + 3/2O2(g) → CO2(g) + 2H2O(l);

ΔrH° = -726 kJ mol-1

(ii) C(g) + O2(g) → CO2(g);

ΔcH° = -393 kJ mol-1

(iii) H2(g) + 1/2O2(g) → H2O(l);

ΔfH° = -286 kJ mol-1

We aim at

C + 2H2 + 1/2 O2 → CH3OH

In order to get this thermochemical equation, multiply Eq. (ii) by 1 and Eq. (iii) by 2 and subtract Eq. (i) from their sum.

C + 2H2 + 1/2O2 → CH3OH

ΔH = (-393) + 2(-286) - (-726)

= -393 - 572 + 726

= -965 + 726 = -239 kJ mol-1

Thus, the heat of formation of CH3OH is

ΔHf = -239 kJ mol-1

1741.

Given: N2(g) + 3H2(g) → 2NH3(g);ΔrH° = -92.4 kJ mol-1What is the standard enthalpy of formation of NH3 gas?

Answer»

ΔfH° NH3(g) = {-(92.4)}/{2} = -46.2 kJ mol-1

1742.

Predict in which of the following entropy increases / decreases.(i) Temperature of a crystalline solid is raised from 0 K to 115 K. (ii) 2NaHCO3 → Na2CO3(s) +CO2 (g) + H2O(g) (iii) H2(g) → 2H(g)

Answer»

(i) When temperature is raised, disorder in molecules increases and therefore entropy increases.

(ii) Reactant is a solid and hence has low entropy. Among the products there are two gases and one solid so products represent a condition of higher entropy. 

(iii) Here 2 moles of H atoms have higher entropy than one mole of hydrogen molecule.

1743.

What is spontaneous process? Give example.

Answer»

Process which takes place itself, without any external aid under the given condition is called spontaneous process. 

Example: Flow of heat from higher to lower temperature.

1744.

Consider the reaction. A + B → C + D (i) If the reaction is endothermic and spontaneous in the direction indicated, comment on the sign of ΔG and ΔS. (ii) If the reaction is exothermic and spontaneous in the direction indicated, can you comment on the sign of G and S? (iii) If the reaction is exothermic and spontaneous only in the direction opposite to the indicated, comment on the sign of AG and AS for the direction indicated in the equation.

Answer»

(i) ΔG = -ve, ΔS = +ve 

(ii) ΔG = -ve, ΔS = -ve (if ΔH > TΔS) 

(iii) ΔG = ΔS = -ve

1745.

Classify the following processes as reversible or irreversible : (i) Dissolution of sodium chloride (ii) Evaporation of water at 373 K and 1 atm. pressure (iii) Mixing of two gases by diffusion (iv) Melting of ice without rise in temperature (b) When an ideal gas expands is vacuum, there is neither absorption nor revolutions of what? why?

Answer»

(a)(i) Irreversible, 

(ii) Irreversible, 

(iii) Irreversible, 

(iv) Reversible 

(b) It is because no work is done, 

i.e., w = 0 w = -pext × ΔV = 0 × ΔV = 0 

In ΔU = q + w 

q = 0 because gas chamber is insulated ΔU = 0 + 0 = 0

1746.

Define non-spontaneous process.

Answer»

Process which does not takes place itself or on its own but with the help of external aid under the given condition is called non-spontaneous process.

Example: Flow of heat energy from lower to higher temperatures.

1747.

(i) What is the value ΔrH° of the following reaction: H+(aq) + OH-(aq) →H2O(l). (ii) Give an example in which enthalpy change is equal to internal energy?

Answer»

(i) ΔrH° = -57.1 kJmol-1 

(ii) H2(g) + I2(g) → 2HI(g) here ΔH = ΔU

1748.

At `25^(@)C`, buring `0.2 "mole" H_(2)` with `0.1` mole `O_(2)` to produce `H_(2)O(l)` in a bomb calorimeter (constant volume) raises the temperature of the apperaturs `0.88^(@)C`. When `0.01mol` toulene is burned in this calorimeter, the temperature is raised by `0.615^(@)C`. Calculate `DeltaH^(Theta)` combustion of toluene. `Delta_(f)H^(Theta) H_(2)O(l) =- 286 kJ mol^(-1)`.

Answer» `Delta_(f)H(H_(2)O) =- 286 kJ "mole"^(-1)`
`{:(H_(2)(g)+,(1)/(2)O_(2)(g)rarr,H_(2)O(l)),(0.2,0.1,0.2):}`
`Deltan_(g) = 0 -(3)/(2) =- (3)/(2)`
`DeltaU = DeltaH - Deltan_(g)RT`
`=- 286 -(-(3)/(2)) xx 8.314 xx 10^(-3) xx 298`
`=- 282.3 kJ mol^(-1)`
`=- 282.3 xx 0.2` (for 0.2 mole)
Heat capacity of calorimetre
`DeltaH = (ms) Deltat`
`(ms) = (DeltaH)/(DeltaT) = (282.3 xx 0.2)/(0.88) = 64.159`
`DeltaH` for `0.01ml` of Toluene
`DeltaU` (atomic constant volume) `= ms xx Deltat`
`= - 64.159 xx 0.615 kJ//0.01 mol`
`=- 39.458 kJ// 0.01 mol`
`=- 39.458 xx 100 kJ mol^(-1)`
`=- 3945.8 kJ mol^(-1)`
`=- 3945.8 kJ mol^(-1)`
`C_(7)H_(8)(l) +9O_(2)(g) rarr 7CO_(2)(g) +4H_(2)O(l)`
`Deltan_(g) = 7 - 9 = -2`
`DeltaH = DeltaU +Deltan_(g)RT`
`=- 3945.8 -2 xx 8.314 xx 10^(-3) xx 298`
`=- 3945.8 -5 =- 3950.8 kJ`mole
1749.

The conversion of gaseous atoms `K` and `F` to `K^(o+)` and `F^(ɵ)` absorbs `0.85 eV` of energy. If the `IE` and `Delta_("eg")H^(ɵ)` of `K` and `F` have magnitudes in the ratio of `7:6`, what is the electron gain enthalpy `(Delta_("eg")H^(ɵ))` of fluorine ?

Answer» Let `IE = xeV`
`E_(A) = yeV`
`:. X -y = 0.85 eV (EA` is exothermic)
`:. x//y = 7//6`
Solved for `x` and `y rArr y = 5.10 eV`
1750.

While `1mol` of ice melts at `0^(@)C` and at constant pressure of `1atm, 1440 cal` of heat are absorbed by the system. The molar volume of ice and water are `0.0196` and `0.0180L` respectively. Calculate `DeltaH` and `DeltaU`.

Answer» `DeltaH = 1440 cal`
`DeltaH = DeltaU +P(DeltaV)`
`[H_(2)O(s)] Ice rarr H_(2)O(l)`
`P DeltaV = (76 xx 13.6 xx 981)/(4.81 xx 10^(-7)) (18 -19.6) (CGS units)`
`= 0.0388cal`
Volume of ice `= 0.0196 L = 19.6 mL`
Volume of `H_(2)O = 0.0180 L = 18 mL`
`DeltaH = DeltaU + 0.0388`
`DeltaU = 1440 - 0.0388 = 1439.96 cal`