N 2(g) +
O 2(g) NO (g),
NO (g) +
O 2(g) NO 2(g) ,
---------------------------------------------------
N 2(g) + O 2(g) NO 2(g)
So, for the reverse reaction which is the desired one the value of K will be reciprocal of this value. i.e. K =
N 2(g) +
O 2(g) NO (g),
NO (g) +
O 2(g) NO 2(g) ,
---------------------------------------------------
N 2(g) + O 2(g) NO 2(g)
So, for the reverse reaction which is the desired one the value of K will be reciprocal of this value. i.e. K =
X 2(g) + 4Y 2(g) 2XY 4(g)
n g = -ve and
H = -ve As
H < 0 i.e., the given reaction is exothermic.
According to Le-Chatelier principle, for exothermic reaction, forward reaction is favoured when temperature becomes low.
Also, there are 5 gaseous moles on reactant side and 2 gaseous moles on products side.
So, forward reaction is favoured when pressure of the reaction mixture becomes high.
The reason is that at high pressure reaction tends to more in direction where there is lessee number of gaseous moles.
<table class=tg> <tbody><tr> <th class=tg-c3ow></th> <th class=tg-9wq8>2A(g)</th> <th class=tg-9wq8>+</th> <th class=tg-c3ow>B(g)</th> <th class=tg-baqh>⇌</th> <th class=tg-baqh>3C(g)</th> <th class=tg-c3ow>+</th> <th class=tg-c3ow>D(g)</th> </tr> <tr> <td class=tg-c3ow>Initial mole</td> <td class=tg-9wq8>1</td> <td class=tg-9wq8></td> <td class=tg-c3ow>1</td> <td class=tg-baqh></td> <td class=tg-baqh>0</td> <td class=tg-c3ow></td> <td class=tg-c3ow>0</td> </tr> <tr> <td class=tg-baqh>At equilibrium</td> <td class=tg-baqh>1 - (2 0.25)<br>= 0.5</td> <td class=tg-baqh></td> <td class=tg-baqh>1 - 0.25<br>= 0.75</td> <td class=tg-baqh></td> <td class=tg-baqh>3 0.25<br>= 0.75</td> <td class=tg-baqh></td> <td class=tg-baqh>0.25</td> </tr> </tbody></table> <br><br>Equilibrium constant, K =
<br><br> K =
As we know, K p = K c × (RT)
n g So, for reaction having same number of gaseous moles on reactants and products side will have same value of Kc and Kp otherwise their values are different.
For reaction, 2NO (g) N 2(g) + O 2(g)
n g = 2 – 2 = 0 K p = K c × (RT) 0 K p = K c For reaction, SO 2(g) + NO 2(g) SO 3(g) + NO (g)
n g = 2 – 2 = 0 K p = K c × (RT) 0 K p = K c For reaction, H 2(g) + I 2(g) 2HI (g)
n g = 2 – 2 = 0 K p = K c × (RT) 0 K p = K c For reaction, H 2(g) + I 2(g) 2HI (g)
n g = 2 – 2 = 0 K p = K c × (RT) 0 K p = K c For reaction, 2C (s) + O 2(g) 2CO 2(g)
n g = 2 – 3 = -1 K p = K c × (RT) -1 K p K c
CH 3 COOH CH 3 COO – + H + , K 1 = 1.5 10 5 K 1 =
= 1.5 10 5 HCN CN – + H + , K 2 = 4.5 × 10 –10 K 2 =
= 4.5 × 10 –10 CN + CH 3 COOH HCN + CH 3 COO K =
K =
=
= 3.33 × 10 4
3.0 × 10 4
Given <br><br>X Y + Z . . . .(i) <br><br>A 2B . . . .(ii) <br><br>Let the total pressure for reaction (i) and (ii) be P<sub>1</sub> and P<sub>2</sub> respectively, then <br><br>
<br><br> <table class=tg> <tbody><tr> <th class=tg-c3ow></th> <th class=tg-9wq8>X</th> <th class=tg-c3ow>⇌ </th> <th class=tg-c3ow>Y</th> <th class=tg-c3ow>+</th> <th class=tg-c3ow>Z</th> </tr> <tr> <td class=tg-c3ow>Initial mole</td> <td class=tg-9wq8>1</td> <td class=tg-c3ow></td> <td class=tg-c3ow>0</td> <td class=tg-c3ow></td> <td class=tg-c3ow>0</td> </tr> <tr> <td class=tg-c3ow>At equilibrium</td> <td class=tg-c3ow>1 - </td> <td class=tg-c3ow></td> <td class=tg-c3ow></td> <td class=tg-c3ow></td> <td class=tg-c3ow></td> </tr> </tbody></table> <br><br>Total number of moles at equilibrium <br><br>= 1 - + + = 1 + <br><br> K<sub>P<sub>1</sub></sub> =
=
<br><br> <table class=tg> <tbody><tr> <th class=tg-c3ow></th> <th class=tg-9wq8>A</th> <th class=tg-c3ow>⇌</th> <th class=tg-c3ow>2B</th> </tr> <tr> <td class=tg-c3ow>Initial mole</td> <td class=tg-9wq8>1</td> <td class=tg-c3ow></td> <td class=tg-c3ow>0</td> </tr> <tr> <td class=tg-c3ow>At equilibrium</td> <td class=tg-c3ow>1 - </td> <td class=tg-c3ow></td> <td class=tg-c3ow>2</td> </tr> </tbody></table> <br><br>Total number of moles at equilibrium <br><br>= 1 - + 2 = 1 + <br><br> K<sub>P<sub>2</sub></sub> =
=
<br><br>
<br><br>
<br><br>
HI (g)
H 2(g) +
I 2(g) , For this reaction, K = 8.0 Reversing the equation,
H 2(g) +
I 2(g) HI (g) ......(1) For this reaction, K 1 =
H 2(g) + I 2(g) 2HI (g) We get this equation by multiplying equation (1) by 2, For this reaction, K 2 =
=
<table class=tg> <tbody><tr> <th class=tg-c3ow></th> <th class=tg-9wq8>2AB2(g)</th> <th class=tg-c3ow>⇌</th> <th class=tg-c3ow>2AB(g)</th> <th class=tg-c3ow>+</th> <th class=tg-c3ow>B2(g)</th> </tr> <tr> <td class=tg-c3ow>Initial mole</td> <td class=tg-9wq8>2</td> <td class=tg-c3ow></td> <td class=tg-c3ow>0</td> <td class=tg-c3ow></td> <td class=tg-c3ow>0</td> </tr> <tr> <td class=tg-c3ow>At equilibrium</td> <td class=tg-c3ow>2(1 - x)</td> <td class=tg-c3ow></td> <td class=tg-c3ow>2x</td> <td class=tg-c3ow></td> <td class=tg-c3ow>x</td> </tr> </tbody></table> <br><br>Amount of moles at equilibrium = 2(1 – x) + 2x + x = 2 + x <br><br>
<br><br>=
<br><br>=
<br><br> K<sub>p</sub> =
<br><br>( 1 – x ≈ 1 and 2 + x ≈ 2) <br><br> x =
<br><br> x =
Fe(OH) 3(s) Fe 3+ (aq) + 3OH (aq) Equilibrium constant, K c =
We know, equilibrium constant remains same at constant temperature.
Now, let the increase in concentration of Fe 3+ be x times.
K c =
=
K c =
K c
= 1 x = 64
2NH 3 N 2 + 3H 2 ;
N 2 + O 2 2NO ; K 2 3H 2 +
O 2 3H 2 O; (K 3 ) 3 By adding all equations, we get 2NH 3 +
O 2 2NO + 3H 2 O K =