A buffer is prepared by dissolving 0.0250 mol of sodium nitrate in 250.0 ml of 0.0410 M of nitrous acid HNO2. Assume no volume change after HNO2 is dissolved. Calculate the ph of this buffer.
The pKa is equal to the negative logarithm to the base 10 of Ka it's basically the measure of the acid dissociation constant. do you kinda get what i'm saying?
here's a little more info to your question Determine molarity of acid and conjugate base 1) acid = 0.0410M 2) conj. base = 0.025/0.25 = 0.10M pKa HNO2 = 3.40
it's hard for me to explain because this is backwards but here lets start off with the Henderson–Hasselbalch equation: pH = pKa + log( [base] / [acid] ) where [base] is the concentration of the conjugate base of the weak acid, and [acid] is the concentration of the weak acid itself. So if the problem states that you have n times as much base as you have acid, you will solve for pKa: pKa = pH - log( n ) pKa ≈ pH midway, because [acid] = [base] and log( 1 ) = 0.
pH = pKa + log (0.1/0.041)
so you don't understand kPa right? but the rest you do understand?
Yes
pKa = pH - log( n ) this is the equation to find pKa but we are missing our pH so thats what we need to figure out
yes
pH = pKa + log( [base] / [acid] ) this is how you find out pH so what is the base? and what is the acid? those are the two easiest right now im going to delete my previous answers they are a bit confusing
this is what we are dealing with
I did the negative log of 1.4 E ^-4.
I got 3.85 I dont know if Im heade in the right direction.
Chemistry: Principles And Reactions : A Core Text
is this your text?
your not doing it right
1) acid = 0.0410M 2) conj. base = 0.025/0.25 = 0.10M pKa HNO2 = 3.40 From the Henderson - Hasselbalch equation: pH = pKa + log ([salt]/[acid]) pH = 3.4 + log ( 0.1/0.041) pH = 3.4 + log ( 2.439) pH = 3.4 + 0.39 pH = 3.79 pKa = pH - log( n ) lets work backwards lets just assume the gave as the ph okay? so solve pKa
I looked in the book it says that pka = -log, -pka= log of ka, and 10^-pka and =10^logka=ka.
that works too lets do that then
I took the negative log of 1.4 E -4. I got 3.85.Then I took 3.85 and raised it to 10^-3.85 and got 1.41E -4 again.
okay just keep on doing what your doing what do you think you have to do after that? are you unsure
I'm sorry I'm not able to explain this well
Its fine
do you know the heylman equation?
http://en.wikipedia.org/wiki/Acid_dissociation_constant http://en.wikipedia.org/wiki/Henderson%E2%80%93Hasselbalch_equation http://en.wikipedia.org/wiki/PH http://answers.yahoo.com/question/index?qid=20100717115344AA8ugwr If you have a buffer solution that is midway to the equivalence point of a titration, pH ≈ pKa (for the titration of a weak acid with a strong base). If you are not midway, but you are still working with a buffer solution, you can use the Henderson–Hasselbalch equation: pH = pKa + log( [base] / [acid] ) where [base] is the concentration of the conjugate base of the weak acid, and [acid] is the concentration of the weak acid itself. So if the problem states that you have n times as much base as you have acid, you will solve for pKa: pKa = pH - log( n ) pKa ≈ pH midway, because [acid] = [base] and log( 1 ) = 0. Determine molarity of acid and conjugate base 1) acid = 0.0410M 2) conj. base = 0.025/0.25 = 0.10M pKa HNO2 = 3.40 From the Henderson - Hasselbalch equation: pH = pKa + log ([salt]/[acid]) pH = 3.40 + log ( 0.1/0.041) pH = 3.4 + log ( 2.439) pH = 3.40 + 0.39 pH = 3.79 I have to leave I have work but I'll help you out later heres some links and pretty much everything you need to know check out the yahoo answers like i think it will be helpful i'm so so sorry i couldn't explain this to you well bye~ also really read the wikipedia ones they have all the equations and how to solve them reply to your message is correct continue and do that!
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