Preparation Of Oxalate Complexes Of Iron Biology Essay

Preparation Of Oxalate Complexes Of Iron Biology EssayTo take a crap two oxalate knottyes of urge namely, thousand Trioxalatoferrate Trihydrate and Iron Oxalate and to analyse the harvest-tides for beseech and oxalate respectively. one and only(a) of the properties known to be characterised by spiritual rebirth coats such as iron is colonial ion take a hopation since they are able to form stable complexes. In this experiment, two complex of iron are be organize with the oxalate ion existence the common ligand in both. green Trioxalatoferrate (III) Trihydrate and Iron (II) Oxalate are the two complexes being formed and are represented by the following chemical structures experience 1 Chemical structures of super C Trioxalatoferrate (III) Trihydrate and Iron (II) Oxalate respectively.The oxalate ion, a let out from play acting as a Lewis base keep be referred to as a bidentate ligand since an oxalate ion croup donates two pairs of electrons (one from each oxygen) to the iron (III) or Iron (II) cation acting as a Lewis venereal disease from two oxygen atoms as can be seen in figure 1 preceding(prenominal).Iron can form a variety of complexes with most of them having an octahedral geometry. In this experiment, the Iron (II) oxalate formed is characterised by an Fe2+ as the central metal cation. This is so oxidate to Fe3+ in establish to synthesise the kelvin Trioxalatoferrate (III) Trihydrate complex characterised by an Fe3+ as the central metal cation.Certain complexes such as the Potassium Trioxalatoferrate (III) Trihydrate complex are tottering to light and therefore they are said to be p live(a)osensitive. For this reason, it is a must to store such a complexes under sulky conditions in stray to forestall the reduction of the Fe3+ ion back to the Fe2+ ion.The amount of oxalate within a complex can be determined using titrimetric analysis. Potassium permanganate is titrated with the oxalate ion and the amount of oxalate can be deter mined through this oxidoreduction titration. No index finger is needed in such a titration due to the situation that the blockpoint is characterised by a listless pick apart colour resulting from the fact that at the end point, excess un fight backed permanganate ions are present in the theme since all the oxalate ions would get to been consumed.The amount of iron in a complex on the separate hand can be analysed following the addition of zinc to the complex solution followed by rut. Once this is carried out, the resulting solutions can be treat with kB permanganate in a redox titration as described previously above and hence, the amount of iron in a complex can be determined.In this experiment, heating is involved in the redox titrations due to the fact that since the opposeion is rather slow at room temperature, in tell for one to observe a quick colour change at the end point, the solution needs to be heated to around 60oC. modeChemicals usedferrous ammonium ion sulphate hydrogen peroxidesulphuric social diseaseEthanolOxalic acid coatFerrous oxalatePotassium permanganatePotassium oxalateApparatus usedBuchner funnelHeating mantleBurette weigh boatThermometerFilter paperMagnetic stirrerGlass sheepskinAnalytical balanceMeasuring cylinderProcedure position a Preparation of Iron (II) oxalate15g of ferrous ammonium sulphate were decided in 50mL warm water which had been acidified with 1mL 2M sulphuric acid.To this, a solution of 10% 75mL oxalic acid was added with rapid stirring. The pastiche was gently heated until its boiling point was reached and the lily-livered precipitant of ferrous oxalate formed was allowed to settle.The precipitate was outside by filtration on a Buchner funnel and washed thourally with hot water followed by acetone.The resultion was allowed to dry on a funnel under suction and was then weighed.Part B Preparation of Potassium Trioxalatoferrate (III) Trihydrate.3.25g of ferrous oxalate was suspended in a warm s olution of (5g in 15mL water) potassium oxalate.To this, 15mL 20 vol. Hydrogen peroxide was added from a burette whilst the solution was stirred continuously and the temperature was maintain at 40oC.The solution contained a precipitate of ferric hydroxide and this was removed by heating the solution to its boiling point and adding 10mL 10% oxalic acid. encourage small amounts of oxalic acid was added drop wise until the precipitate just turn.The hot solution was filtered and 15mL ethanol was added to the filtrate in shape to re pick any crystals that formed by gentle heating.The solution was identifyd in a dark cupboard to crystallize since the product formed was photosensitive.The crystals were stash away by filtration on a Buchner funnel and later washed with an equivolume mixture of ethanol and water followed by acetone. The crystals were then dried and weighed.Part C The analysis of the products for Iron and OxalateFor Iron (II) oxalate0.3g of oxalate were dissolved in 25 mL 2M sulfuric acid and the solution was heated to 60oC and titrated with 0.2M standard potassium permanganate solution until the first permanganate pink colour was notice.2g of zinc pitter-patter was added and the solution was boiled for 25 minutes. The solution was filtered through glass wool and the residual zinc was washed with 2M sulfuric acid.The washings were added to the filtrate and the solution was titrated with standard potassium permanganate.The percentages of iron, oxalate and water of recrystalisation in the product were determined and hence, the observational reflexion could be derived.For Potassium trioxalatoferrate (III) trihydrate0.2g of Potassium trioxalatoferrate (III) trihydrate were dissolved in 25mL 2M sulfuric acid and titrated with 0.02M permanganate.The solution was treated with zinc dust and re-titrated with permanganate as described in the analysis of Iron (II) oxalate above.The percentages of iron and oxalate in the complex were determined and this w as compared to the theoretical value.PrecautionsIt was made sure that in the eagerness of Potassium Trioxalatoferrate (III) Trihydrate, ethanol was added to the filtrate in order to re dissolve any crystals that formed by gentle heating.It was made sure that in the set of Potassium Trioxalatoferrate (III) Trihydrate, the solution was placed in a dark cupboard to crystallize since the product formed was photosensitive.It was made sure that for the preparation of Potassium Trioxalatoferrate (III) Trihydrate, the temperature was maintained at 40oC to prevent hydrogen peroxide decomposition.ObservationsFerrous (II) oxalate had a sensationalistic precipitate and at the end a yellow powder was obtained.The endpoint of the redox titrimetric titration was marked by a faint pink colouration.Ferric hydroxide had a brown precipitate which false into a green solution upon excess oxalic acid was added.Potassium Trioxalatoferrate (III) Trihydrate formed was in the form of green crystals.3. Re sults and CalculationsResultsPart AFerrous ammonium sulphate weighed 15.042g10% oxalic acid measured 75mLMass of ferrous (II) oxalate obtained 5.586gPart BFerrous (II) oxalate used 3.269gPotassium oxalate used 5.008gMass of Potassium Trioxalatoferrate (III) Trihydrate obtained 2.205gPart CFerrous (II) oxalate used 0.320gPotassium Trioxalatoferrate (III) Trihydrate used 0.200gZinc used 2g raft of permanganate required in the redox titration amid iron (II) oxalate and permanganate 49.5mL downes of permanganate required in the redox titration between iron (II) oxalate and permanganate in the presence of zinc 15.50mLVolume of permanganate required in the redox titration between Potassium Trioxalatoferrate (III) Trihydrate and permanganate 24.50mLVolume of permanganate required in the redox titration between Potassium Trioxalatoferrate (III) Trihydrate and permanganate in the presence of zinc 4.00mLCalculationsAnalysis of products for Iron Oxalate for Iron(II) oxalateThe e quations taking place in the reaction are2MnO4- (aq) + 5C2O42- (aq) + 16H+ (aq) 2Mn2+ (aq) + 10CO2 (g) + 8 water (l)5Fe2+ + MnO4- + 8H+ 5Fe3+ + Mn2+ + H2OMoles permanganate reacting with oxalate and iron = Concentration of permanganate x Volume of permanganate requiredMoles permanganate = 0.02 x (49.50 / deoxycytidine monophosphate0)Moles permanganate = 0.00099 molesMoles permanganate reacting with iron (II) = Concentration of permanganate x Volume of permanganate requiredMoles permanganate = 0.02 x (15.5 / 1000)Moles permanganate = 0.00031 molesTherefore, moles of permanganate reacting with the oxalate ions = Total recite of moles Number of moles of permanganate reacting with iron.0.00099 0.00031= 0.00068 molesFrom the stoichiometry of the equation it is notice that 2 moles of permanganate react with 5 moles of oxalate, and soMoles of oxalate = 5/2 (0.00068) = 0.0017 molesGrams of oxalate = depend of moles x bunch of oxalateGrams of oxalate = 0.0017 x 88Grams of oxalate = 0.150 gramsTherefore % oxalate in the product(0.150 / 0.320) x 100 = 46.9 %From the stoichiometry of the equation it is detect that 1 mole of permanganate react with 5 moles of Iron, thusMoles of oxalate = 5 (0.00031) = 0.00155 molesGrams of Iron (II) = number of moles x flock of oxalateGrams of Iron (II) = 0.00155 x 56Grams of Iron (II) = 0.087 gramsTherefore % Iron in the product(0.087 / 0.320) x 100 = 27.19%The mass of water = Total mass of complex (Mass of oxalate + iron (ii))Mass of water = 0.320 (0.150 + 0.087) = 0.083gTherefore moles = grams / RMMMoles water = 0.083 / 18Moles water = 0.0046 molesTherefore % water in product(0.083 / 0.320) x 100 = 25.9%To calculate the empirical formulaIron Oxalate Water0.00155 0.0017 0.00460.00155 0.00155 0.001551 1 3Thus empirical formula is FeC2O4.3H2OAnalysis of products for Iron Oxalate for Potassium trioxalatoferrate (III) trihydrate.The equation taking place in the reaction are2MnO4- (aq) + 5C2O42- (aq) + 16H+ (aq) 2Mn2+ (aq ) + 10CO2 (g) + 8H2O (l)5Fe2+ + MnO4- + 8H+ 5Fe3+ + Mn2+ + H2OMoles permanganate reacting with oxalate = Concentration of permanganate x Volume of permanganate requiredMoles permanganate = 0.02 x (24.5 / 1000)Moles permanganate = 0.00049 molesFrom the stoichiometry of the equation it is observed that 2 moles of permanganate react with 5 moles of oxalate, thusMoles of oxalate = 5/2 (0.00049) = 0.00123 molesGrams of oxalate = number of moles x mass of oxalateGrams of oxalate = 0.00123 x 88Grams of oxalate = 0.108 gramsTherefore % oxalate in the product(0.108 / 0.200) x 100 = 54 %Moles permanganate reacting with iron (III) = Concentration of permanganate x Volume of permanganate requiredMoles permanganate = 0.02 x (4.00 / 1000)Moles permanganate = 810-5 molesFrom the stoichiometry of the equation it is observed that 1 mole of permanganate react with 5 moles of Iron, thusMoles of oxalate = 5 (810-5) = 0.0004 molesGrams of Iron = number of moles x mass of oxalateGrams of Iron = 0.0004 x 56Grams of Iron = 0.0224 gramsTherefore % Iron in the product(0.0224 / 0.200) x 100 = 11.20%DiscussionIn the first part of the experiment, ferrous ammonium sulphate, also known as Mohrs Salt was treated with warm water and sulphuric acid in order to prevent the formation of rust coloured iron hydroxides and oxides. This was followed by oxalic acid. The oxalate ions replace some or all of the sulphate ligands surrounding the Fe2+ ion and as a result, a yellow precipitate of ferrous oxalate forms. The reaction taking place is as followsH2C2O4 (aq) + Fe2+ (aq) + 2H2O (l) 3H2O+ (aq) + FeC2O4 (s)In order to oxidise the Fe2+ ion into an Fe3+ ion in ferrous oxalate, hydrogen peroxide, acting as an oxidising agent is added to a solution of ferrous oxalate and potassium oxalate. Temperature work is very crucial in this step due to the fact at high temperatures, hydrogen peroxide can decompose and thus would not be able to oxidise the iron (II) to iron (III) required to cook the Potassiu m trioxalatoferrate (III) trihydrate complex. It is important to make sure that all the iron (ii) has been oxidised to iron (iii) due to the fact that since each complex consists of a polar number of oxalate ligands, if a mixture of the two complex ions is present, the empirical formula determination would become difficult. The reaction taking place is as follows2FeC2O4 (s) + C2O42- (aq) + H2O2 (aq) + 2H3O+ (aq) 4H2O (l) + Fe2(C2O4 )3 (s)When the Fe2(C2O4 )3 precipitate was dissolved, Fe(C2O4)33- forms. This reacts with the potassium ions in solution introduced via the potassium oxalate and forms potassium trioxalatoferrate (III) which is photosensitive and thus must be stored in the dark.In the analysis of the oxalate ion, no indicator is required in the redox titration between permanganate and the oxalate ions due to the fact that at the end point, since potassium permanganate is an oxidising agent, it oxidises the oxalate ions in solution into carbon dioxide and as a result, pe rmanganate is itself reduced to Mn2+ therefore a faint pink colour is observed at the endpoint. The reactions taking place are as follows2MnO4- (aq) + 5C2O42- (aq) + 16H+ (aq) 2Mn2+ (aq) + 10CO2 (g) + 8H2O (l)In order to analyse the iron content in the complexes formed, zinc is added followed by heating the solution. Once this was complete, the solution was treated with permanganate in a redox titration comparable to the one described previously above. The reaction taking place is as follows5Fe2+ + MnO4- + 8H+ 5Fe3+ + Mn2+ + H2OConclusionThis experiment has shown that iron being a transition metal can exist as various oxidisation states. These oxidation states can then form a variety of complexes with various ligands. The complexes that are formed can then be analysed using a redox titration in order to determine the percentages of iron and oxalate in the complex.In this experiment, the empirical formula of Iron (II) oxalate was found to be FeC2O4.3H2O and consisted of 46.9 % ox alate, 27.19% Iron (II) and 25.9% water where as the Trioxalatoferrate (III) Trihydrate consisted of 54% oxalate and 11.20% iron (III)