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Sunday, September 17, 2023

Titration of Weak acid Vs Strong base:

 (II):  Titration of Weak acid Vs Strong base:

Titration of a weak acid by strong base is a bit more complex than both acid and base are strong this is because we have consideration the equilibrium involving the weak acid and its conjugate base.

Titration Table and curve:

S.N

 Acid (0.1M)  

Base (0.1M )   

pH

Nature

 Case

1

 

0  ml

2.85

WA

pH=1/2(Pka –logC)

2

Volume

5 ml

4.22

ABS

pH=(Pka +log [S]/[A]

3

Taken

10 ml

4.7

ABS

pH=Pka Best Buffer

4

20.0 ml

15 ml

5.17

ABS

pH=(Pka +log [S]/[A]

5

Ka for

19 ml

5.98

ABS

pH=(Pka +log [S]/[A]

**6

CH3COOH

20 ml

8.7

SH

pH=7+1/2(Pka+logC)

7

2* 10^-10

21 ml

11.39

SB

NbVb - NaVa=NrVr

8

 

25 ml

12.04

SB

[OH-]= Nr

9

 

30 ml

12.3

SB

Strong base

10

 

 

 

 

Remains present

 



In titration of any weak acid with strong base, The pH at equivalent point will be greater than “7”

TITRATIONS OF DIPROTIC ACID WITH STRONG BASE:

Sunday, September 10, 2023

The thermodynamics equilibrium constant Kp for the homogeneous gaseous reaction is 10^-3. The standard Gibb's free energy change ∆G° for the reaction at 27°C. (Use R= 2 cal K ^−1 mol ^−1) is :

Calculate the pH of 1.0×10^−3 M sodium phenolate NaOC6​H5​ . Ka​ for C6​H5​OH is 1×10^−10 .

ΔG^ o at 25^°C for the reaction 1/2N2(g) + 3/2H2(g) ⇋ 2NH3(g) is -11.392 kj mole^-1. Hence thermodynamics equilibrium constant is : he equilibrium constant for reaction is 10. (Use R=8.3 JK ^−1 mol ^−1)

Answer key : 10^2

The dissociation equilibrium of a gas AB2 can be represented as : 2AB2(g) ⇋ 2AB(g) + B2(g) The degree of dissociation is "x" and is small compared to 1. The expression relating the degree of dissociation (x) with equilibrium constant Kp and total pressure P is.

(A) (2KP/P)^1/2  
(B) (KP/P) 
(C) (2KP/P) 
(D) (2KP/P)^1/3

Saturday, September 2, 2023

Gibb's free energy (∆G) and Equilibrium constant (Kc):

The part f energy which is converted into usefull work called Gibb's free energy or Gibb's function.
 
Energy (H) = Useful work (G) + Non useful (TS)

We van not calculate absolute value of 'G' so we calculate change in Gibb's free energy. 

             ∆G = ∆H -∆TS
       ∆G = ∆H - (∆TS + T∆S). ......(1)

Standard Gibb's energy (∆G°) change at  standard condition is 1 bar  and 298 K

             ∆G° = ∆H° -∆TS°  .......(2) 

Relation between ∆G° and Equilibrium constant (K):




Factor's Affecting Equilibrium Constant

(1) Le-Chetelier'e principle
(i) Effect of change in  temperature
(ii) Effect of change in  concentration 
(iii) Effect of change of volume of container at equilibrium
(iv) Effect of change in pressure
(v) Effect of Catalyst at equilibrium
(vi) Effect of Addition of Inert gas
(a) At constant volume
(b) At constant pressure 

          [End of Chapter = ∆∆∆]

Application of Equilibrium Constant (K):

(1) Predicting extent of reactions
(2) Predicting of stability of reactants and products
(3) Predicting direction of reactions at any instant of reaction (Qc)
(4) Predicting concentration of reactants and products at equilibrium.
(5) Degree of dissociation and Kp and Kc in term of DOD.
(6) Degree of dissociation and Vapour density.