The ICE table is as follows: H 2 I 2 HI 601
The ICE table is as follows: H 2 I 2 HI 602
The ICE table is as follows: H 2 I 2 HI – y – y y 603
The ICE table is as follows: H 2 I 2 HI – y – y y 604
Now think about any possible simplification. 605
Now think about any possible simplification. There is none! 606
Math Aside: The quadratic equation 607
Math Aside: The quadratic equation A quadratic equations looks like: 608
Math Aside: The quadratic equation A quadratic equations looks like: 609
Math Aside: The quadratic equation A quadratic equations looks like: The solutions (there are two of them) take the form 610
Math Aside: The quadratic equation A quadratic equations looks like: The solutions (there are two of them) take the form 611
Math Aside: The quadratic equation A quadratic equations looks like: The solutions (there are two of them) take the form Note that in an equilibrium problem, only one of the solutions will generate a physically acceptable solution to the problem. 612
We now need to solve 613
We now need to solve 614
We now need to solve 615
We now need to solve 616
We now need to solve Now solve the quadratic equation using with a = 50.3, b = , and c = 8.99x
618
y = M or y = M. 619
y = M or y = M. The first answer is physically impossible. 620
y = M or y = M. The first answer is physically impossible. Why? 621
y = M or y = M. The first answer is physically impossible. Why? The concentration of I 2 = – y = M which is physically impossible. We cannot have a negative concentration. 622
y = M or y = M. The first answer is physically impossible. Why? The concentration of I 2 = – y = M which is physically impossible. We cannot have a negative concentration. So the solution we seek is y = M. 623
At equilibrium: 624
At equilibrium: [H 2 ] = – = M 625
At equilibrium: [H 2 ] = – = M [I 2 ] = – = M 626
At equilibrium: [H 2 ] = – = M [I 2 ] = – = M [HI] = x = M 627
At equilibrium: [H 2 ] = – = M [I 2 ] = – = M [HI] = x = M Check: 628
At equilibrium: [H 2 ] = – = M [I 2 ] = – = M [HI] = x = M Check: 629
There is a simple way to tell which way the reaction will proceed to equilibrium. 630
There is a simple way to tell which way the reaction will proceed to equilibrium. Consider H 2(g) + I 2(g) 2 HI (g) and suppose all three gases are present at the start of the reaction. 631
There is a simple way to tell which way the reaction will proceed to equilibrium. Consider H 2(g) + I 2(g) 2 HI (g) and suppose all three gases are present at the start of the reaction. The reaction quotient is where the initial concentrations are employed. 632
There is a simple way to tell which way the reaction will proceed to equilibrium. Consider H 2(g) + I 2(g) 2 HI (g) and suppose all three gases are present at the start of the reaction. The reaction quotient is where the initial concentrations are employed. If Q c > K c there must be too much HI in the mixture for equilibrium to exist. Consequently, the reaction will proceed from right to left, until Q c becomes equal to K c. 633
There is a simple way to tell which way the reaction will proceed to equilibrium. Consider H 2(g) + I 2(g) 2 HI (g) and suppose all three gases are present at the start of the reaction. The reaction quotient is where the initial concentrations are employed. If Q c > K c there must be too much HI in the mixture for equilibrium to exist. Consequently, the reaction will proceed from right to left, until Q c becomes equal to K c. If Q c < K c, the reaction will proceed left to right. 634
In many equilibrium problems, the equilibrium constant is very small. This allows a simplification of the mathematics, so that the general quadratic equation does not have to be solved. 635
In many equilibrium problems, the equilibrium constant is very small. This allows a simplification of the mathematics, so that the general quadratic equation does not have to be solved. Example 3: 1.00 moles of N 2 is placed in a 1.00 liter vessel along with 1.10 moles of O 2 at 25 o C. Calculate the amount of NO formed at 25 o C. K c = 4.8 x at 25 o C for the reaction N 2(g) + O 2(g) 2 NO (g). 636
The ICE table is as follows: N 2 O 2 NO 637
The ICE table is as follows: N 2 O 2 NO 638
The ICE table is as follows: N 2 O 2 NO 639
The ICE table is as follows: N 2 O 2 NO 1.00 – y 1.10 – y 2y 640
The ICE table is as follows: N 2 O 2 NO 1.00 – y 1.10 – y 2y 641
Now 642
Now At this point, always stop and look for any possible simplifications. 643
Now At this point, always stop and look for any possible simplifications. Notice that we do not have a perfect square on the right-hand side. 644
Now At this point, always stop and look for any possible simplifications. Notice that we do not have a perfect square on the right-hand side. In this case there is a mathematical simplification on the right-hand side of the equation – 645
Now At this point, always stop and look for any possible simplifications. Notice that we do not have a perfect square on the right-hand side. In this case there is a mathematical simplification on the right-hand side of the equation – what is it? 646
Now At this point, always stop and look for any possible simplifications. Notice that we do not have a perfect square on the right-hand side. In this case there is a mathematical simplification on the right-hand side of the equation – what is it? Notice that K c is very small, which means very little product will be formed. 647
Since y is very small, we try the approximations: 1.00 – y – y
Since y is very small, we try the approximations: 1.00 – y – y 1.10 We will check momentarily the quality of these approximations. The equilibrium constant expression simplifies to 649
Since y is very small, we try the approximations: 1.00 – y – y 1.10 We will check momentarily the quality of these approximations. The equilibrium constant expression simplifies to K c 650
Since y is very small, we try the approximations: 1.00 – y – y 1.10 We will check momentarily the quality of these approximations. The equilibrium constant expression simplifies to K c 651
Since y is very small, we try the approximations: 1.00 – y – y 1.10 We will check momentarily the quality of these approximations. The equilibrium constant expression simplifies to K c So y = 3.6 x M. 652
Since y = 3.6 x M the approximations 1.00 – y – y 1.10 are justified. At equilibrium: [NO] = 2 y = 7.2 x M 653
When can approximations be made to simplify equilibrium constant expressions? 654
When can approximations be made to simplify equilibrium constant expressions? The only places where approximations can be made are (where A and B are concentrations): 655
When can approximations be made to simplify equilibrium constant expressions? The only places where approximations can be made are (where A and B are concentrations): (A – y) A where A >> y 656
When can approximations be made to simplify equilibrium constant expressions? The only places where approximations can be made are (where A and B are concentrations): (A – y) A where A >> y and (B + y) B where B >> y 657
When can approximations be made to simplify equilibrium constant expressions? The only places where approximations can be made are (where A and B are concentrations): (A – y) A where A >> y and (B + y) B where B >> y Never in places like y (A – y) or 658
Le Châtelier’s Principle 659
Le Châtelier’s Principle We will examine the effect of the following on the equilibrium constant. 660