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- Acid-base definitions
- Chemistry of buffers and buffers in our blood
- Ka and acid strength
- Autoionization of water
- Definition of pH
- Strong acid solutions
- Strong base solutions
- Weak acid equilibrium
- Weak base equilibrium
- Relationship between Ka and Kb
- Acid–base properties of salts
- pH of salt solutions
- Common ion effect and buffers
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Weak base equilibrium
Quick overview of Kb and pKb. Examples of calculating the pH of a weak base solution.
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- By finding the ph of ammonia, shouldn't we technically be solving for the pOH since ammonia is a base. It makes no sense to me that the pH is a larger number than the pOH. I would expect the pH to be 2.52 and pOH to be 11.48(0 votes)
- Keep in mind that a pH >7 is classified as a base and a pH < 7 is considered acidic .
We know that ammonia is a base so we expect the pH to be above 7.
Remember that pH + pOH = 14
This can be rearranged to pH = 14 - pOH
If the pOH was larger than the pH then the solution would have to be acidic.(12 votes)
- Why do we say that the concentration of pure liquids and solids is one? Is it molarity? If it is, are we saying that there is always one mole of the solid/liquid in every litre of the solid/liquid?(3 votes)
- It is the activity of the liquids and solids that equals 1.
The concentration of water is 55.5 mol/L. The typical concentration of a solute in a reaction
is 0.1 mol/L to 1 mol/L.
Even if the water is a reactant in the reaction, its concentration stays almost constant.
We can consider that its constant is incorporated into the equilibrium constants K_a, K_b. and K_w.(5 votes)
- I don't understand why we assume that .003 is for the OH. Couldn't it be for the NH4+ also since they are both set to x?!(3 votes)
- You are correct,
xrepresents both the [OH¯] and [NH₄⁺].
Why do you think that is a problem?
Remember the goal was to work out the pH, so [OH¯] matters while [NH₄⁺] does not ...(5 votes)
- how come we can assume that x<< 0.500 or x<< 1 in the two examples discussed above?(4 votes)
- let us consider the case of NH3. x in the above example is the concentration of NH4+ and OH- formed ( also called degree of ionization), and we know that NH3 is a weak base. Since Weak bases ( or acids) only disassociate by a very small amount, the conc. of NH4+ and OH- ( which is x) is very small. Hence we ignore it to simplify our calculations, and assume that 0.5 - x is almost the same as 0.5. Hope this helped :)(1 vote)
- At 0.05, why does the water donate proton and ammonia don't?Why ammonia can't act as acid? How to figure out which one donates proton and which one not?(2 votes)
- That is because NH2 (it's apparently written as H2N- and called azanide) is a better base than water. So for that reason NH3 will have to be the Bronsted-Lowry Acid here. You'd usually know which way it goes by practicing and seeing questions after all the range of compounds you will be given will be limited and you'd normally instantly be knowing the answer.(1 vote)
- for example at0:45(as with previous videos), why is the B-L definition of a base used when the Lewis definition is more inclusive?(3 votes)
- The B-L definition touches more on bases having one less proton (H+) that acids, relating more on the Arrhenius definition.(1 vote)
- why did you mention concentration as I and not C?(1 vote)
- I stands for initial concentration
C stands for change in concentration
E stands for equilibrium concentration(4 votes)
- Does Pka for bases exists and can we predict ionization strenth of the same(2 votes)
- We can only make these mathematical assumptions with weak acids or bases, correct?(1 vote)
- You only need to do so with weak acids and bases yes(2 votes)
- that number the Ka and Kb are they indicating m/liter? or some kind of proportion?(1 vote)
- K values are dimensionless in terms of units.
You could think of it as the ratio of the number of molecules of products to the number of molecules of reactants.(2 votes)
- Ammonia is a weak base, and if ammonia reacts with water water is gonna function as a Brønsted–Lowry acid. Water is going to donate a proton to ammonia, and ammonia is going to accept the proton. It's going to be a Brønsted–Lowry base. Lone pair of electrons in the nitrogen pick up this proton which leaves these electrons behind on the oxygen. If you protonate ammonia you form ammonium, the ammonium ion which is NH4 plus. Let's show those electrons. These electrons, these lone pair of electrons here on the nitrogen pick up this proton and form this bond right here. We form NH4 plus, and these electrons in blue come off on to the oxygen. The oxygen had two lone pairs of electrons around it. And the electrons in blue are now around it which give it a negative 1 formal charge here. We form the ammonium ion, NH4 plus, and the hydroxide ion, OH minus. If ammonia functioned as a Brønsted–Lowry base over here would be the conjugate acid. Ammonium is the conjugate acid to NH3. Water functioned as a Brønsted–Lowry acid. Over here would be the conjugate base, the hydroxide anion. Instead of using ammonia let's just do a generic base. Here I have B written. Some generic base reacts with water. It takes a proton from water to form BH plus. If you take a proton away from H2O you would form OH minus. Once this comes to equilibrium we could write an equilibrium expression. We're gonna write Kb here. Instead of Ka we're now writing Kb because we're talking about a base. Kb can be called, you can call this the base ionization constant. Let me write base ionization constant here. Or you could call this the base dissociation constant, so base dissociation constant. When you're writing an equilibrium expression remember it's the concentration of your products over your reactants. Over here we have the concentration of BH plus times the concentration of OH minus. That's all going to be over the concentration of your reactants, so we leave out water so we have only the concentration of our generic base, B. You could think about Kb the same way we thought about Ka. The higher the value for Kb the stronger the base because the more of your products you are going to make here. Let me go ahead and write that. The stronger the base the larger the value for large for Kb. Let's talk about two weak bases here. We've already mentioned ammonia, and we're going to compare ammonia to aniline. NH3 is ammonia, and the Kb for ammonia is 1.8 times 10 to the negative 5. Aniline is C6H5NH2. Notice it has a lower value for the Kb, 4.3 times 10 to the negative 10 is a much smaller number, a much smaller value than 1.8 times 10 to the negative 5. Ammonia has a higher value for the Kb, and therefore it's a stronger base than aniline. Once again, both of them are weak bases but ammonia is the stronger of the two. Remember when we talked about Ka we also talked about pKa. We're gonna do the same thing here. We've talked about Kb, and so now let's talk about calculating the pKb. The pKb is equal to the negative log of the Kb. Let's say we wanted to find the pKb for ammonia. All we'd have to do is plug in the Kb value. The pKb would be equal to the negative log of 1.8 times 10 to the negative 5. Let's get out the calculator here and do the problem. Negative log of 1.8 times 10 to the negative 5. We get 4.74 here. The pKb for ammonia is 4.74. You could do the same calculation for aniline and plug in this Kb, and you would get a pKb of 9.37. Comparing two weak bases, ammonia and aniline, ammonia is the stronger of the two because it has a higher value for the Kb. And notice that the pKb is a lower value, so once again analogous to what we talked about for pKa. Next we do a calculation for a solution of ammonia. Our problem asks us to calculate the pH of a 0.500 molar solution of aqueous ammonia. We have ammonia in water. We have NH3 plus H2O. Ammonia is going to accept a proton from water and turn it into NH4 plus, ammonium. If water loses a proton H2O turns into OH minus. Let's go ahead and write our initial concentration here. For ammonia we have 0.500 molars. We write 0.500 molar here. And we're pretending like nothing has happened, so the concentration of our products is 0. Nothing has happened yet so the concentration of ammonium is 0, and the concentration of hydroxide is also 0. Next let's think about the change. Since ammonia, since NH3 turns into NH4 plus, the concentration of ammonia that's lost is the same concentration as ammonium that is gained. If we represent that concentration using X, if we lose a certain concentration of ammonia that's the same concentration of ammonium that we gain. This would be plus X over here for ammonium. It'd be the same thing for hydroxide. This would be a plus X here for the hydroxide anion. Therefore at equilibrium, for ammonia, the concentration of ammonia at equilibrium we would have 0.500 minus X. For ammonium we would have X, and for hydroxide we would also have X. Next we write our equilibrium expressions, so we write Kb here is equal to the concentration of our products, so that's NH4 plus, so I write NH4 plus here, times the concentration of hydroxide. That's all over the concentration of ammonia. We leave water out, so this all over the concentration of ammonia here. Let's plug in what we know. At equilibrium the concentration of ammonium is X. Let's write in an X here for the concentration of ammonium. And it's the same thing for the concentration for hydroxide. For hydroxide, the concentration at equlibrium is also X. We write an X right here. This is all over the concentration of ammonia and that would be the concentration of ammonia at equilibrium is 0.500 minus X. We put in 0.500 minus X here. This is all equal to the base ionization constant for ammonia. Let's go back up to our table above to remind ourselves of what it is. Ammonia has a Kb of 1.8 times 10 to the negative 5. We're gonna plug that value in for Kb here. This is equal to 1.8 times 10 to the negative 5. Once again we're going to assume that X is much, much smaller than 0.500 molar because that makes our life easy for the math. We don't have to do the quadratic formula if we do that. If we make this assumption that 0.500 minus X, if X is extremely small, this is pretty much the same thing as 0.500. We're going to leave that out. Let's rewrite what we have here. We have 1.8 times 10 to the negative 5 is equal to, this would be X squared over 0.500. All we have to do now is solve for X. We would have X squared is equal to, let's see, 1.8 times to 10 to the negative 5, we have to multiply that by 0.5 and we would get 9.0 times 10 to the negative 6. Next we just take the square root of 9.0 times 10 to the negative 6 to solve for X. Let's go ahead and do that. Let's get out the calculator here and let's take the square root of 9.0 times 10 to the negative 6. We get 0.003. Let's go ahead and write, X is equal to 0.0030. Remember what X refers to. Let's go back up here. Let's think about what X is talking about. X is talking about a concentration and notice we have an X here for our concentration of hydroxide anions. That's what's going to allow us to eventually get the pH which is what the question asked for. X is equal to the concentration of hydroxide anions. This would be molar. This is our concentration of hydroxide anions. Our goal is, once again, to find the pH of our solution. First we could find the poH. That's one way to do it. The poH is equal to the negative log of the concentration of hydroxide ions. We could go ahead and take the negative log of 0.0030 to calculate the poH of our solution. Let's do that on our calculator. Negative log of 0.0030 is equal to 2.52. The poH is equal to 2.52. Then to find the pH all we have to do is subtract from 14 because pH plus poH is equal to 14. I believe in a previous video I forgot to put these zeros here. We're concerned about significant figures. You plug in your poH into here, so your pH plus 2.52 is equal to 14.00. You just solve for pH. pH is equal to 14 minus 2.52 which is 11.48. Finally we've calculated the pH of our solution of ammonia.