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ocr a f325 revision thread

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Reply 1660
Original post by drplease
Do we have to know the indicators?? It says on the spec guess I will have to cram it...


nope we dont where one spec does it say that?
Reply 1661
Original post by DudeBoy
June 2010
7b.
You times by 34 as that is the Ar of H2O2
2(1)+2(16)


thanks don't know why I didnt find that lol

Original post by DudeBoy
Jan 2011
7ai. Use CV/1000 to get S2O3(2-) used.
=2.46x10^-5

Look at the equations, 2 moles of S2O3 form 2 moles of I(-)
So I(-) = 2.46x10^-5
2 mole of I(-) reacts 2 moles of Mn(OH)3 so =2.46x10^-5.
4 moles of Mn(OH)3 is formed by 1 mole of O2, so O2 moles = mole of O2 = 2.46x10^-5/4.
=6.15x10^-6

Use CV/100 to get conc of O2.


This method doesn't work because
If I go to OH- instead of Mn(OH)3, this is what happens:
2 mole of I(-) reacts 2 moles of OH- so =2.46x10^-5.
8 moles of OH- is formed by 1 mole of O2, so O2 moles = mole of O2 = 2.46x10^-5/8.
=3.08x10^-6

Different answer.
Reply 1662
Original post by Namod
nope we dont where one spec does it say that?


'(p) for acid–base titration pH curves for strong
and weak acids and bases:
(i) interpret, or sketch, their shapes,
(ii) explain the choice of suitable indicators
for acid–base titrations, '

In case they may not give you indicators, hence you may need to name one closest to equivalence point
Reply 1663
Original post by drplease
'(p) for acid–base titration pH curves for strong
and weak acids and bases:
(i) interpret, or sketch, their shapes,
(ii) explain the choice of suitable indicators
for acid–base titrations, '

In case they may not give you indicators, hence you may need to name one closest to equivalence point


"explain the choice" "State the indicator that must be used"
Big difference mate.

GL :biggrin:
(edited 10 years ago)
after in depth revision, began ppq... i got a low b at first mark, a B it still is lool... definitely more area for improvements...hws it going?
Original post by MathsNerd1
What challenging questions could actually be asked on transition metals/elements as I'm struggling to see where they become challenging :redface: Same with all the calculation questions too.


Try jan 13 last q.
Original post by DudeBoy
It is D. AgOH⇌Ag(+) + OH(-)
If Ag(+) is added it reacts with OH(-) thus decreasing the Kc value.
pH may also decrease, but I am not sure because there will be less OH(-) ions.


Thats wrong. chiggy guy is right. kc not affected by changesa in conc
Original post by Gulzar
But I just looked in the book and they carried out a enthalpy of neutralisation calculation pg 156...using degrees C and not Kelvin :s-smilie:



Original post by Better
Go in the internet and search SI Units. Degrees C, is not an SI Unit.

The Examples in the book are just Examples. All of these Papers I have done work on Kelvin.

If you convert to Degrees C AFTER you've done the calculation they will give you a mark but you will get it wrong if you do it before, as you will use the wrong number.

Change temp for neutralisation so wouldnt matter k or c
Original post by MedMed12
YAAAY really? :O I hope I get that now :tongue: means I can get a B in unit 4 -_-
I doubt we'll get papers like the old ones though :frown: heard they are toughening up!
the boundaries are nice for this paper! :smile:
my friend had a theory that everyone should enter for all exams (only work for 4 subjects they are sitting) and everyone else in the room who doesn't need/study chem should just sleep and get Us and it'll lower the grade boundaries for chem-takers! Clever thing huh? :tongue:


Waste of money..
(edited 10 years ago)
Reply 1669
Original post by Theafricanlegend
Thats wrong. chiggy guy is right. kc not affected by changesa in conc


if the concentration changes, the equilibrium shift to decease the effects, so Kc will remain constant, only thing that change the Kc is change in temperature

if reaction exothermic= *increase the temp-> equilibrium shifts to left hence Kc decrease
*decrease the temp -> equilibrium shifts to right, hence Kc increases

if reaction endothermic= *increase the temp-> equilibrium shifts to the right, Kc increases
*decrease the temp -> equilibrium shifts to the left, Kc decrease

Kc=[products]/[reactants]
Reply 1670
Original post by Theafricanlegend
Try jan 13 last q.


Hi, do you have F325 jan 13, can you please give me the link, or upload it here, many thanks :smile:
Original post by amin666
Hi, do you have F325 jan 13, can you please give me the link, or upload it here, many thanks :smile:


Here ya go
Reply 1672
For a standard hydrogen electrode. What is the actual electrode, is it Platinum wire? or is it Platinum foil at the bottem of the gas imput thingy
Original post by amin666
if the concentration changes, the equilibrium shift to decease the effects, so Kc will remain constant, only thing that change the Kc is change in temperature

if reaction exothermic= *increase the temp-> equilibrium shifts to left hence Kc decrease
*decrease the temp -> equilibrium shifts to right, hence Kc increases

if reaction endothermic= *increase the temp-> equilibrium shifts to the right, Kc increases
*decrease the temp -> equilibrium shifts to the left, Kc decrease

Kc=[products]/[reactants]

i know that.
You didnt need to write it.
Original post by Theafricanlegend
i know that.
You didnt need to write it.


no need to be rude!
Reply 1675
Hi, doing some extra questions but surely this answer that it says on the mark scheme is wrong?

This is the question: Calculate the pH of a buffer solution that is 0.100 mol dm–3 with respect to sodium methanoate and 0.200 mol dm–3 with respect to methanoic acid. The Ka of methanoic acid is 1.8 × 10–4 mol dm–3.

I did Ka x Acid/Salt and then -log10 of the H+ conc to give me a pH of 3.44 from a H+ of 3.6 x10-4


However, the mark scheme says this:

[HCOOH(aq)]eqm 0.100 mol dm–3 and [HCOO–(aq)]eqm 0.200 mol dm–3
Ka = [HCOO–(aq)]eqm[H+(aq)]
[HCOOH(aq)]eqm
So [H+(aq)] = 9.0 × 10–5 mol dm–3
pH = 4.05

^^ is this not wrong? If not can someone explain where I am wrong please. Thank you.
Does ionisation constant mean the same as Ka?
Original post by ofudge
Hi, doing some extra questions but surely this answer that it says on the mark scheme is wrong?

This is the question: Calculate the pH of a buffer solution that is 0.100 mol dm–3 with respect to sodium methanoate and 0.200 mol dm–3 with respect to methanoic acid. The Ka of methanoic acid is 1.8 × 10–4 mol dm–3.

I did Ka x Acid/Salt and then -log10 of the H+ conc to give me a pH of 3.44 from a H+ of 3.6 x10-4


However, the mark scheme says this:

[HCOOH(aq)]eqm 0.100 mol dm–3 and [HCOO–(aq)]eqm 0.200 mol dm–3
Ka = [HCOO–(aq)]eqm[H+(aq)]
[HCOOH(aq)]eqm
So [H+(aq)] = 9.0 × 10–5 mol dm–3
pH = 4.05

^^ is this not wrong? If not can someone explain where I am wrong please. Thank you.


u're right. where is this q from/?
Reply 1678
Original post by otrivine
Does ionisation constant mean the same as Ka?


You talking about the ionic product of water?

If you are, it's similar. ka= [OH-][H+]/[h2O]
As H2O is constant, they move it to other side and KAx[H2O]=Kw=[OH-][H+]
Original post by otrivine
Does ionisation constant mean the same as Ka?


http://lmgtfy.com/?q=ionisation+constant

heehee

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