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Synthesis of Copper (II) Oxalate Complex

This document details an experiment focused on synthesizing Copper (II) Oxalate Complexes, outlining the procedures, results, and calculations involved. The experiment achieved a percentage yield of 98.25% with a final product mass of 2.817g, indicating an effective synthesis process despite some discrepancies with theoretical yields. The findings highlight the importance of transition metals in forming complex ions and the potential for errors due to reactant impurities.

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0% found this document useful (0 votes)
20 views3 pages

Synthesis of Copper (II) Oxalate Complex

This document details an experiment focused on synthesizing Copper (II) Oxalate Complexes, outlining the procedures, results, and calculations involved. The experiment achieved a percentage yield of 98.25% with a final product mass of 2.817g, indicating an effective synthesis process despite some discrepancies with theoretical yields. The findings highlight the importance of transition metals in forming complex ions and the potential for errors due to reactant impurities.

Uploaded by

parkseonghwapurr
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd

1.

0 INTRODUCTION

In this experiment, it is to understand the process of synthesizing the Copper (II)


Oxalate Complexes where in this case, we will talk about the step-by-step process for
making copper (II) oxalate complexes. We will also talk about the chemical reactions that
make them, the methods used in the experiments, and how they might be characterised.

Oxalates, derived from oxalic acid or its salts, serve as bidentate ligands capable of
forming stable complexes with metal ions. The synthesis of copper (II) oxalate complexes
typically involves the reaction between a copper salt and oxalic acid or its sodium or
potassium salts. This process leads to the precipitation of a distinctive copper (II) oxalate
compound. Oxalate complexes are coordination compounds produces by reacting oxalic
acid with a transition metal. For copper (II) oxalate K2[Cu(C2O4)2(H2O)2] complexes,
copper transition metal that acts as a Lewis acid while the oxalate ion as well as water act
as Lewis bases.

The amount of yield form can be calculated using theoretical yield which mass of
coordination compound times the molar mass of the compound.
2.0 OBJECTIVE
1. To prepare a copper (II) oxalate complex.
3.0 PROCEDURE
4.0 RESULTS AND DATA

Mass of copper (II) sulphate pentahydrate 2.024


Mass of empty petri dish (g) 31.458
Mass of petri dish + precipitate (g) 34.275
Mass of product (g) 2.817

Appearance of the product: blue-white solid (as a hemihydrate)


1. Theoretical yield of 𝐾2 [𝐶𝑢(𝐶2 𝑂4 )2(𝐻2 𝑂2 )] : 2.867 g
2. Mass of 𝐾2 [𝐶𝑢(𝐶2 𝑂4)2(𝐻2 𝑂2 )] obtained. : 2.817 g
3. Percentage yield of 𝐾2 [𝐶𝑢(𝐶2 𝑂4 )2(𝐻2 𝑂2 )] : 98.25%
CALCULATION
A complete balance reaction:
𝐶𝑢𝑆𝑂4 . 5𝐻2 𝑂 + 2𝐾2 𝐶2 𝑂4 . 𝐻2 𝑂 → 𝐾2 [𝐶𝑢(𝐶2 𝑂4 )2]. 𝐾2 𝑆𝑂4 + 5𝐻2 𝑂
a. To find the limiting reactant:

Experimental mass of 𝐶𝑢𝑆𝑂4 . 5𝐻2 𝑂 : 2.024 g

1 𝑚𝑜𝑙𝑒 𝐶𝑢𝑆𝑂 .5𝐻 𝑂 [𝐶𝑢(𝐶 𝑂 )2]


2.024 g 𝐶𝑢𝑆𝑂4 . 5𝐻2 𝑂 x 249.72 𝑔 𝐶𝑢𝑆𝑂4.5𝐻2𝑂0 x 1 𝑚𝑜𝑙𝑒2 𝑜𝑓4 𝐾 : 0.008105 mol
4 2 2

Experimental mass of 𝐾2 𝐶2 𝑂4 . 𝐻2 𝑂 : 6.235 g

1 𝑚𝑜𝑙𝑒 𝐾 𝐶 𝑂4 .𝐻2 𝑂 [𝐶𝑢(𝐶 𝑂 )2]


6.235 g 𝐾2 𝐶2 𝑂4 . 𝐻2 𝑂 x 184.218 𝑔 2𝐾 2𝐶 x 1 𝑚𝑜𝑙𝑒2 𝑜𝑓4 𝐾 : 0.034 g
2 2 𝑂4 .𝐻2 𝑂 2

- The limiting reactant is 𝐶𝑢𝑆𝑂4 . 5𝐻2 𝑂

b. To find theoretical yield:


Theoretical yield = mol of limiting reactant x molar mass of product
= 0.008105 x 353.82 g mol
= 2.867 g
c. To find percentage of yield:
Actual yield = 2.817 g
Percentage yield = (actual yield/theoretical yield) x 100%
= (2.817 / 2.867) x 100%
= 98.25%
Percentage error = (theoretical yield – actual yield) / theoretical yield x 100%
= (2.867 – 2.817) / 2.867 x 100%
= 1.74%
5.0 DISCUSSION
In this experiment, during copper (II) oxalate complex is synthesised, transition metals
such as copper have a greater propensity to form complex ions. To begin with, the reaction
between potassium oxalate monohydrate and copper (II) sulphate pentahydrate produced a
coordination compound known as copper (II) oxalate complex. After combining the heated
copper (II) sulphate and potassium oxalate in a vessel that had been cooled for a certain time,
a quantity of precipitate developed, which had a dark blue colour. The solution was filtered
through suction filtration, which resulted in the collection of the blue crystal, and subsequently
rinsed with chilled water. The bulk of the crystal was then determined by weighing it after it
had dried.
The total weight of the copper (II) oxalate complex that was synthesised was measured
to be 2.817g. The obtained mass, which is significantly below the theoretical yield of 2.867g,
corresponds to a yield percentage of 98.25%. Although the substantial percentage yield implies
a synthesis process that is effective, the disparity between the masses obtained and those
predicted signifies possible error sources that may have occurred throughout the experiment.
Reactant or reagent impurities have the potential to reduce the efficacy of a given reaction.
Potential consequences of contaminants include the generation of undesired by-products and
disruption of the coordination process.
6.0 CONCLUSION
As the conclusion, the objective had been achieved as to prepare a copper (II) oxalate
complex had been successfully conduct with a total weight obtained is 2.817g and percentage
yield of 98.25%. The appearance of the product also blue-white solid (as a hemihydrate)
proofing that a formation has happened.
7.0 REFERENCES
1. John Rumble (June 18, 2018). CRC Handbook of Chemistry and Physics (99 ed.). CRC
Press. pp. 5–188. ISBN 978-1138561632
2. Raymond Chang and Kenneth A. Goldsby, Chemistry 11th Edition Published by Mc Graw
Hill (2013), page 758-1002.

3. [1]“What is a Complex Ion?,” Chemistry LibreTexts, Oct. 03, 2013.


[Link]
Websites_(Inorganic_Chemistry)/Coordination_Chemistry/Structure_and_Nomenclature_of_
Coordination_Compounds/What_is_a_Complex_Ion

Common questions

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The percentage yield of 98.25% indicates a highly efficient process, implying minimal loss of product and effective reaction conditions. Achieving nearly complete yield suggests precise control over reaction parameters and inherent stability in the formation of the copper (II) oxalate complex .

The purification of the copper (II) oxalate complex involves suction filtration to separate the precipitated coordination compound from the reaction mixture. The precipitate is then rinsed with chilled water to remove impurities. The characterization of the compound is inferred from its appearance as a blue-white solid and by measuring its mass to confirm yield efficiency, achieving a 98.25% yield against the theoretical prediction, indicating the compound's successful formation .

In the synthesis, the limiting reactant is determined by comparing the molar amounts of CuSO4·5H2O and K2C2O4·H2O used. CuSO4·5H2O is the limiting reactant because it results in fewer moles of product compared to the amount of K2C2O4·H2O available. Identifying the limiting reactant is crucial as it dictates the maximum possible yield of the copper (II) oxalate complex and ensures calculations for theoretical yield are accurate .

The synthesis of copper (II) oxalate complex involves the reaction of copper (II) sulfate pentahydrate and potassium oxalate monohydrate. Copper (II) acts as a Lewis acid and the oxalate ion and water act as Lewis bases. The reaction forms a coordination compound where the oxalate serves as a bidentate ligand creating stable complexes with copper ions. The final product, K2[Cu(C2O4)2(H2O)2], precipitates as a blue-white solid due to the formation of this coordination complex .

Water acts as a ligand in the copper (II) oxalate complex by donating lone pairs of electrons from the oxygen atoms to the central copper ion. This coordination helps stabilize the metal complex, impacting its solubility and structural properties, and plays a critical role alongside oxalate ions in forming the coordination sphere .

Oxalic acid and its salts serve as bidentate ligands, which are key for forming stable metal complexes due to their ability to donate electron pairs to metal centers. In copper (II) complexes, this results in strong, stable bonding within the coordination sphere, leading to distinct physical properties and high stability of the resulting copper (II) oxalate complex .

Copper (II) oxalate complexes exemplify coordination chemistry as they involve central metal ions bound to surrounding ligands (oxalate and water). The oxalate acts as a bidentate ligand, enhancing bonding stability and forming a distinct three-dimensional structure, reflecting coordination compound characteristics such as coordination number and geometric arrangement .

Suction filtration is used to efficiently separate solid precipitates from the reaction mixture quickly and with reduced risk of secondary contamination or loss of the product. It offers advantages in achieving a dry, pure sample rapidly, which is essential for further processing and accurate yield calculations .

Potential sources of error include impurities in the reactants, inaccuracies in measurements, or incomplete reactions. These could result in undesired by-products or interruptions in the coordination process, reducing reaction efficacy. The difference between theoretical and actual yield (only 1.74% error) suggests minor errors, yet this highlights the necessity of purity and accuracy for optimal syntheses .

Thermodynamics plays a key role in complex formation, where the stability of the copper (II) oxalate complex is influenced by enthalpy and entropy changes. The coordination bonds formed release energy, stabilizing the system (enthalpic favorability), while the ordered structure may reduce randomness (entropic penalty). The balance of these factors drives the reaction towards the stable complex formation .

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