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NCERT Solutions For Class 11 Chemistry chapter 6- Thermodynamics

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NCERT Solutions For Class 11 Chemistry chapter 6- Thermodynamics

NCERT Solutions for class-11 Chemistry Chapter 6 Thermodynamics is prepared by our senior and renown teachers of Physics Wallah primary focus while solving these questions of class-11 in NCERT textbook, also do read theory of this Chapter 6 Thermodynamics while going before solving the NCERT questions. Our Physics Wallah team Prepared Other Subjects NCERT Solutions for class 11.

Chapter 6 Thermodynamics

Answer the following Questions.

1. Choose the correct answer. A thermodynamic state function is a quantity

(i) used to determine heat changes

(ii) whose value is independent of path

(iii) used to determine pressure volume work

(iv) whose value depends on temperature only

Solution :

A thermodynamic state function is a quantity Whose value is independent of a path. Functions like p, V, T etc. depend only on the state of a system and not on the path.

Hence, alternative (ii) is correct.


2. For the process to occur under adiabatic conditions, the correct condition is:

(i) ∆T = 0

(ii) ∆p = 0

(iii) q = 0

(iv) w = 0

Solution : A system is said to be under adiabatic conditions if there is no exchange Of heat between the system and its surroundings. Hence, under adiabatic conditions, q = 0.

Therefore, alternative (iii) is correct,


3. The enthalpies of all elements in their standard states are:

(i) unity

(ii) zero

(iii) < 0

(iv) different for each element

Solution : The enthalpy of all elements in their standard state is zero. Therefore, alternative (ii) is correct


4. ΔU of combustion of methane is −X kJ mol −1 . The value of ΔH⊖ is

(i)=ΔU

(ii) >ΔU

(iii) <=ΔU

(iv) = 0

Solution :

SinceΔH θ =ΔU θ +Δn g RT and ΔU θ =−Xkmol −1

ΔH θ =(−X)+Δn g RT

⇒△H θ <ΔU θ

Therefore, alternative (iii) is correct.


5. The enthalpy of combustion of methane, graphite and dihydrogen at 298 K are, –890.3kJmol −1 −393.5kJmol −1 , and −285.8kJmol −1

respectively. Enthalpy of formation of CH 4 will be

(i)−74.8kJmol −1

(ii)−52.27kJmol −1

(iii)+74.8kJmol −1

(iv)+52.26kJmol −1

Solution :

According to the question,

(i)CH 4 (g)+2O 2 (g)⟶CO 2 (z)+2H 2 O(g)ΔH=−890.3kJmol −1

(ii)C(x)+O 2 (y)⟶CO 2 (g)ΔH=−393.5kJmol −1

(iii)2H 2 (g)+O 2 (z)⟶2H 2 O(g)

ΔH=−285.8kJmol −1

Thus, the desired equation is the one that represents the formation of CH 4 (g) i.e..,

pw

= [-395.5 + 2(-285.8) - (-890.3)] kJ Mol -1

= -74.8 kJ Mol -1

∴ Enthalpy of formation of CH 4 (g)=−74.8kJmol −1 Hence, alternative (i) is correct.

6. A reaction, A + B → C + D + q is found to have a positive entropy change. The reaction will be
(i) possible at high temperature
(ii) possible only at low temperature
(iii) not possible at any temperature
(iv) possible at any temperature

Solution :
For a reaction to be spontaneous, ΔG should be negative.
ΔG = ΔH – TΔS
According to the question, for the given reaction,
ΔS = positive
ΔH = negative (since heat is evolved)
⇒ ΔG = negative
Therefore, the reaction is spontaneous at any temperature.
Hence, alternative (iv) is correct.


7. In a process, 701 J of heat is absorbed by a system and 394 J of work is done by the system. What is the change in internal energy for the process?

Solution :

According to the first law of thermodynamics,
ΔU = q + W    (i)
Where,
ΔU = change in internal energy for a process
q = heat
W = work
Given,
q = + 701 J (Since heat is absorbed)
W = –394 J (Since work is done by the system)
Substituting the values in expression (i), we get
ΔU = 701 J + (–394 J)
ΔU = 307 J
Hence, the change in internal energy for the given process is 307 J.


8. The reaction of cyanamide,NH 2 CN(s) with dioxygen was carried out in a bomb calorimeter, and ∆U was found to be –742.7kJmol −1 at 298 K. Calculate enthalpy change for the reaction at 298 K.

NH 2 CN(g) + 3/2O 2 (g)→N 2 (g)+CO 2 (g)+H 2 O(l)

Solution :

Enthalpy change for a reaction (ΔH) is given by the expression,
ΔH = ΔU + Δn g RT
Where,
ΔU = change in internal energy
Δn g = change in number of moles
For the given reaction,
Δng = ∑n g (products) – ∑n g (reactants)
= (2 – 1.5) moles
Δn g = 0.5 moles
And,
ΔU = –742.7 kJ mol –1
T = 298 K
R = 8.314 × 10 –3 kJ mol –1 K –1
Substituting the values in the expression of ΔH:
ΔH = (–742.7 kJ mol –1 ) + (0.5 mol) (298 K) (8.314 × 10 –3 kJ mol –1 K –1 )
= –742.7 + 1.2
ΔH = –741.5 kJ mol –1


9. Calculate the number of kJ of heat necessary to raise the temperature of 60.0 g of aluminium from 35°C to 55°C. Molar heat capacity of Al is 24 Jmol −1 K −1 .

Solution :

From the expression of heat (q) q=m⋅ c. ΔT

Where,

c= molar heat capacity

m= mass of substance

ΔT= change in temperature

Substituting the values in the expression of q:

q=(60/27mol)(24Jmol −1 K −1 )(20K)

q=1066.7J

q=1.07k


10. Calculate the enthalpy change on freezing of 1.0 mol of water at10.0°C to ice at

–10.0°C.ΔfusH=6.03kJmol−1 at 0 C

C p [H 2 O(I)]=75.3Jmol −1 K−1

C ρ [H 2 O(s)]=36.8Jmol −1 K −1

Solution :

Total enthalpy change involved in the transformation is the of the following changes:

(a) Energy change involved in the transformation of 1 mol of water at 10 C to 1 mol of water at 0 C.

(b) Energy change involved in the transformation of 1 mol of water at 0∘  to 1 mol of ice at 0 C

(c) Energy change involved in the transformation of 1 mol of ice at0∘C to 1 mol of ice at−10 C.

ΔH= C p [ H 2 OCl]ΔT+ ΔH fivering + C ρ [H 2 O (s) ]ΔT

=(75.3] mol −1 K −1 )(0−10)K + (−6.03 × 10 3 Jmol −1 )+(36.8] mol −1 K −1 )(−10 −0)K

=−7533 mol −1 − 6030Jmol −1 − 368Jmol −1

=−7151J mol −1

=−7.151kJmol −1

Hence, the enthalpy change involved in the transformation is−7.151kJmol −1 .


11. Enthalpy of combustion of carbon to CO 2 is –393.5−7.151kJmol −1 . Calculate the heat released upon formation of 35.2 g ofCO 2 from carbon and dioxygen gas.

Solution :

Formation of CO 2 from carbon and dioxygen gas can be represented as:

C(s) + O 2 (g)⟶CO 2 (g)

Δ f H=−393.5kJmol −1

(1 mole =44g) Heat released on formation of 44gCO 2 =−393.5kJmol−1

∴ Heat released on formation of 35.2gCO 2

=−314.8kJmol −1


12. Enthalpies of formation of CO(g), CO 2 (g), N 2 O(g) and N 2 O 4 (g) are −110,−393,81 and 9.7kJmol −1 respectively.

Find the value of ∆H for the reaction:

N 2 O 4 (g)+3CO(g)→N 2 O(g+3CO 2 (g]

Solution :

Δ r H for a reaction is defined as the difference between ΔH value of products and ΔH value of reactants.

Δ,H=∑Δ,H( products )−∑Δ f H( reactants )

For the given reaction,

N 2 O 4(g) + 3CO (g) ⟶ N 2 O (g) + 3CO 2 (g)

Δ r H=[ {ΔfH(N 2 O)+3ΔJH(CO 2 )}−{ΔfH (N 2 O 4 ) + 3ΔjH(CO)} ]

Substituting the values ofΔH for N 2 O,CO 2 ,N 2 O 4 , and CO

From the question, we get:

Δ r H=[ { 81kJmol −1 + 3(−393)kJmol −1 } − {9.7kJmol −1 +3(−110) kJmol −1 }]

Δ r H=−7777kJmol −1

Hence, the value ofΔ r H

for the reaction is −777.7 kJmol −1 .


13. Given

N 2 (g) + 3H 2 (g) ⟶ 2NH 3 (y);

Δ r Hθ=−92.4kJmol −1

What is the standard enthalpy of formation ofNH 3 gas?

Solution : Standard of formation of a compound is the charge in enthalpy that takes place during the formation of 1 mole Of a substance in its standard form from its constituent elements in their standard state.

Re-writing the given equation for 1 mole of NH 3(g).

1/2N 2 (g)+3/2H 2 (g)⟶NH 3(g)

∴ Standard enthalpy of formation of NH 3(g)

=1/2 Δ r Hθ = 1/2(−92.4 kJmol −1 )= −46.2kJmol −1


14. Calculate the standard enthalpy of formation ofCH 3 OH(l)  from the following data:

CH 3 OH(l)+3/2O 2 (g]→CO 2 (g)+2H 2 O(l): Δ,H∘=−726kJmol −1

C(graphite) +O 2 (g)→CO2(g]: ΔeH=−393kJmol −1

H 2 (g)+1/2O 2 (g)→H 2 O(1); Δ,H=−286kJmol −1

Solution :

The reaction that takes place during the formation ofCH 3 OH(l) can be written as:

C(s) + 2H 2 O(g) + 1/2O 2 (G), ⟶ CH 3 OH( η) (1)

The reaction (I) can be obtained from the given reactions by following the algebraic calculations as:

Equation (ii) + 2 × equation (iii) – equation (i)
Δ f Hθ [CH 3 OH(l)] = ΔcH θ + 2Δ f H θ [H 2 O(l)] – Δ r H θ
= (–393 kJ mol –1 ) + 2(–286 kJ mol –1 ) – (–726 kJ mol –1 )
= (–393 – 572 + 726) kJ mol –1
Δ f H θ [CH 3 OH(l)] = –239 kJ mol –1


15. Calculate the enthalpy change for the process CCl 4 (g)→C(g)+4Cl(g) and calculated bond enthalpy of C−Cl in CCl 4 (g)

Δ va pH θ (CC|4) = 30.5kJmol −1 Δ f H θ (CCl4) =−135.5kJmol−1

Δ a H θ (C) = 715.0kJmol −1 , where Δ a H θ is enthalpy of atomisation

Δ 2 H θ (Cl 2 ) = 242kJmol −1

Solution :

The chemical equations implying to the given values of enthalpies” are:
(1) CCl 4(l) à CCl 4(g) ; ΔvapH Θ = 30.5 kJmol −1
(2) C (s) à C (g) ΔaH Θ = 715 kJmol −1
(3) Cl2 (g) à 2Cl (g) ; Δ a H Θ = 242 kJmol −1
(4) C (g) + 4Cl (g) à CCl 4(g) ; ΔfH Θ

= -135.5 kJmol −1 ΔH for the process CCl 4(g) à C (g) + 4Cl (g) can be measured as:
ΔH=Δ a H Θ (C) + 2ΔaH Θ (Cl 2 ) – Δ vap H Θ –ΔfH
= (715kJmol −1 ) + 2(kJmol −1 ) – (30.5kJmol −1 ) – (-135.5kJmol −1 )
Therefore, H= 1304kJmol −1
The value of bond enthalpy for C-Cl in CCl 4 (g)
= 1304/4kJmol −1
= 326 kJmol −1


16. For an isolated system, ∆U = 0, what will be ∆S ?

Solution :
ΔS will be positive i.e., greater than zero
Since ΔU = 0, ΔS will be positive and the reaction will be spontaneous.


17. For the reaction at 298 K,

2A + B → C

∆H = 400kJmol −1

and ∆S = 0.2kJmol −1

At what temperature will the reaction become spontaneous considering ∆H and ∆S to be constant over the temperature range.

Solution :

From the expression

ΔG= ΔH−TΔS

Assuming the reaction at equilibrium,δ

T for the reaction would be:

T=(ΔH−ΔG)1/ΔS=ΔH/ΔS(ΔG=0 at equilibrium)

=400kJmol −1 0.2 kJK −1 mol −1 T=2000K

For the reaction to be spontaneous,ΔG must be negative. Hence, for the given reaction to be spontaneous, T should be greater than 2000 K.


18. For the reaction,2Cl(g)→Cl 2 (g) , what are the signs of ∆H and ∆S ?

Solution :

∆H and ∆S are negative

The given reaction represents the formation of chlorine molecule from chlorine atoms. Here, bond formation is taking place. Therefore, energy Is being released. Hence ∆H is negative.

Also, two moles of atoms have more randomness than one mole of a molecule. Since spontaneity is decreased, ∆S is negative for the given reaction.


19. For the reaction

2A(g)+B(g)→2D(g)ΔUe=−10.5kJ and ΔS∘=−44.1JK −1

Calculate ΔG for the reaction, and predict whether the reaction may occur spontaneously

Solution :

For the given reaction,

2A(g)+B(g)→2D(g)Δηg=2−(3)=−1 mole

Substituting the value of ΔU θ

in the expression of ΔH:

ΔH θ =ΔU θ +Δn g RT

=(−10.5kJ)−(−1)(8.314×10 −3 kJK−1 mol −1 ) (298K) = −10.5kJ −2 .48kJΔH =−12.98kJ

Substituting the values ofΔH and ΔS in the expression of ΔG

ΔG θ = △H θ −TΔS θ

=−12.98kJ − ( 298K) (−44.1JK −1 ) = −12.98kJ + 13.14 kJ ΔG =+0.16kJ

SinceΔG θ for the reaction is positive, the reaction will not occur spontaneously.


20. The equilibrium constant for a reaction is 10. What will be the value of ∆G ? R = 8.314JK −1 mol −1

T = 300 K.

Solution :

From the expression, ΔG θ = −2.303 RT logk eq

ΔG θ for the reaction,

=(2.303) (8.314JK −1 mol −1 ) (300K) log10=−5744.14Jmol −1

=−5.744kkmol −1


21. Comment on the thermodynamic stability of NO(g) , given

12N 2(g) +12O 2(g) →NO (g) ;

Δ r H = 90kJmol −1 NO (g) + 12O 2(g) →NO 2 (g):

Δ r H e = −74kJmol −1

Solution :

The positive value of Δ r H indicates that heat is absorbed during the formation of NO(g), j. This means that NO(g) has higher than the reactants(N2 and O2) .

Hence, NO (g) is unstable.  The negative value o f Δ r H

H indicates that heat is evolved during the formation ofNO 2(g) from NO (g) and O 2(g)

. The product,NO 2(g) is stabilized with minimum energy.

Hence, unstableNO (g) changes to unstableNO 2(g).


22. Calculate the entropy change in surroundings when 1.00 mol ofH 2 O(l) is formed under standard conditions.ΔH θ =−286kJ mol −1

Solution :

It is given that 286 kJmol −1 of heat is evolved the formation of 1 mol ofH 2 O(l).

Thus, an equal amount of heat will be absorbed by the surroundings.

q surr = +286 kJmol −1

Entropy change(ΔS surr )  for the surroundings = q surr / 7

=286kJmol −1 / 298k

∴ΔS surt =959.73 Jmol −1 K −1

NCERT Solutions For Class 11 Chemistry Chapter Wise.

  1. Chapter 1 Some Basic Concepts of Chemistry

  2. Chapter 2 Structure of Atom

  3. Chapter 3 Classification of Elements and Periodicity in Properties

  4. Chapter 4 Chemical Bonding and Molecular Structure

  5. Chapter 5 States of Matter

  6. Chapter 6 Thermodynamics

  7. Chapter 7 Equilibrium

  8. Chapter 8 Reodx Reactions

  9. Chapter 9 Hydrogen

  10. Chapter 10 S-Block Elements

  11. Chapter 11 P-Block Elements

  12. Chapter 12 Some Basics Principles and Techniques

  13. Chapter 13 Hydrocarbons

  14. Chapter 14 Environmental Chemistry

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