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KMnO4
formula for potassium permanganate
potassium manganate VII
alternative name for potassium permanganate
purple coloured solid
how does potassium permanganate come in the lab
cannot be obtained in a highly pure state, decomposes in sunlight, decomposes in heat
why is potassium permanganate not a primary standard
Mno4- + 8H+ +5e- = Mn2+ + 4H2O
formula for potassium permanganate acting as an oxidising agent in an acidic solution. it gains 5 e-
+7 purple to +2 colourless
how does the oxidation state of potassium permanganate change in the half reaction as well as colour.
sulfuric acid
what is added to supply KMnO4 with h+ ions so it can undergo redox reaction
the KMnO4 would oxidise it to Cl2
why cant HCL be used instead of H2SO4
brown due to the formation of manganese dioxide MnO2
what colour does the manganese ion change to in a neutral or basic solution
+7 to +4
what oxidation state change occurs to Mn in a basic or neutral solution
self indicating
why dont you need an indicator with KMnO4
read top of meniscus
weird practice with KMnO4
intense colour, low solubility, effective oxidising agent
why do we use dilute potassium permanganate
titrate against Fe2+ ions
how do we determine the concentration of KMnO4
5
how many e- can a MnO4- accept when reacted with Fe2+ ions
1
how many e- can Fe2+ lose to MnO4-
1:5
ratio of KMnO4:Fe2+
not a primary standard (crystals slightly oxidised by air, efflorescent)
why cant Fe2+ be obtained from FeSO4’7H2O
efflorescence
the spontaneous loss of water of crystallisation to the air
ammonium iron II sulfate
where dow e get the Fe2+ ions
(NH4)2’FeSO4’6H20
formula of ammonium iron ii sulfate
well stabilised and isnt efflorescent
why can we use ammonium iron ii sulfate despite it being hydrated
392
relative molecular mass of ammonium iron ii sulfate
prevent Fe2+ from oxidising to Fe3+ by oxygen in the air
why must ammonium iron ii sulfate be dissolved in water containing diluted sulfuric acid
KMnO4
what goes in the burette when standardising a solution of a solution of KMnO4 against ammonium iron ii sulfate
ensure sufficient supply of h+ ions, so all MnO4- are reduced to Mn2+
why is excess sulfuric acid added to the conical flask of ammonium iron ii sulfate when standardising KMnO4 against it
brown precipitate
what happens if no or insufficient sulfuric acid is added to the conical flask for KMnO4 against ammonium iron ii sulfate
purple to clear to pink
colour change seen in the conical flask in the standardising of KMnO4 against ammonium iron ii sulfate m(3, including one excess drop)
KMnO4 again
what goes in the burette when titrating KMnO4 against iron tablets comboed with H2SO4 (sulfuric acid)
yes
is an excess of sulfuric acid added to the iron tablet experiment
purple to clear to pink 2
colour change in iron tablet experiment
Na2S203
sodium thiosulfate formula
colourless crystalline solid hydrated
typical way we find sodium thiosulfate
S2O3 2-
thiosulfate ion formula
I2 + 2S203 2- = S4O6 2- + 2I-
formula for the reaction between iodine and sodium thiosulfate to get a tretrathionate ion
S4O6 2-
tetrathionate ion formula
cant be obtained in a highly pure state, efflorescent
why isnt sodium thiosulfate a primary standard
titrate it against a standard solution of iodine
how do we find out the concentration of sodium thiosulfate
sublimes
why cant a standard solution of iodine be made up by weighing it directly
titrate KMnO4 against excess potassium iodide solution
how do we standardise a solution of iodine
2MnO4- + 10I- + 16h+ = 2Mn2+ + 5I2 + 8H2O
equations between mno4- ion and iodide ion, with the multiplication of 5 and 2
need 5 in other equation
why do we have to multiply the 2I- by 5
we need 2 in the other equation
why do we multiply the mno4- by 2
2:5
ratio of KMnO4 to iodine formed
reddish brown to pale yellow to colourless
colour change in an iodine/thiosulfate titration
pale yellow
when do we add starch to iodine/thiosulfate
blue black to colourless
colour change of starch
will absorb the iodine earlier
why dowe add starch only at colourless