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Commercial washing soda is approximately \(30-40 \% \mathrm{w} / \mathrm{w} \mathrm{Na}_{2} \mathrm{CO}_{3}\). One procedure for the quantitative analysis of washing soda contains the following instructions: Transfer an approximately 4 -g sample of the washing soda to a \(250-\mathrm{mL}\) volumetric flask. Dissolve the sample in about \(100 \mathrm{~mL}\) of \(\mathrm{H}_{2} \mathrm{O}\) and then dilute to the mark. Using a pipet, transfer a \(25-\mathrm{mL}\) aliquot of this solution to a \(125-\mathrm{mL}\) Erlenmeyer flask and add 25 \(\mathrm{mL}\) of \(\mathrm{H}_{2} \mathrm{O}\) and 2 drops of bromocresol green indicator. Titrate the sample with \(0.1 \mathrm{M} \mathrm{HCl}\) to the indicator's end point. What modifications, if any, are necessary if you want to adapt this procedure to evaluate the purity of commercial \(\mathrm{Na}_{2} \mathrm{CO}_{3}\), that is \(>98 \%\) pure?

Short Answer

Expert verified
Reduce sample size for purity analysis, use smaller aliquots if necessary, and titrate to endpoint.

Step by step solution

01

Understanding the Goal

To determine the purity of commercial \(\text{Na}_2\text{CO}_3\) (sodium carbonate), which is claimed to be >98% pure, we must adapt a procedure typically used for washing soda (30-40% \(\text{Na}_2\text{CO}_3\)). This involves evaluating whether the existing titration method needs adjustments when applied to nearly pure sodium carbonate.
02

Analyzing Sample Preparation

The current procedure prepares an aqueous solution from a 4 g sample of washing soda in a 250 mL volumetric flask. Since the concentration of sodium carbonate in pure form is higher, ensure accurate weighing and dissolution of the sample to prevent errors in volumetric analysis due to saturation or incomplete dissolution.
03

Modifying Sample Mass

For nearly pure sodium carbonate, reduce the sample mass transferred to the volumetric flask, as 4 g of very pure substance may cause saturation or supersaturation. Instead, consider using a smaller mass that ensures full dissolution within the 250 mL flask.
04

Adjusting the Aliquot Volume

The procedure transfers a 25 mL aliquot for titration, likely suitable for the washing soda's lower carbonate concentration. For purer \(\text{Na}_2\text{CO}_3\), smaller aliquot volumes may be necessary to prevent excessive titration volume requirements, thus maintaining accuracy and practicality in the titration.
05

Performing the Titration

Titrate the adjusted aliquot using the \(0.1 \, \text{M} \, \text{HCl}\) solution to the same endpoint using a bromocresol green indicator. Record the volume of \(\text{HCl}\) used, which will allow calculation of the purity of the sodium carbonate based on reacted volume.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Volumetric Analysis
Volumetric analysis is a powerful quantitative analytical technique used to determine the concentration of a solute in solution. This method relies on the precise measurement of liquid volumes. In the context of our given problem, volumetric analysis involves preparing the solution of washing soda and subsequently performing titrations. The process starts with the dissolution of the sample in water and the usage of a volumetric flask to adjust the solution to a known volume. A volumetric flask is chosen because it ensures that the volume of the solution is known with high accuracy, which is crucial for reducing errors in quantitative analysis.

The principle behind volumetric analysis is straightforward: by knowing the volume and concentration of one solution (here, the titrant, which is hydrochloric acid), you can calculate the concentration of the other (the analyte, sodium carbonate). The titration utilizes a standard solution to react with the substance being analyzed; in this case, the reaction follows \[\text{Na}_2\text{CO}_3 + 2\text{HCl} \rightarrow 2\text{NaCl} + \text{H}_2\text{O} + \text{CO}_2.\]

Choosing the correct volumes and concentrations is vital for successful titrations since errors in either can lead to inaccurate results. In the procedure you're working with, making sure the known or standard solution is of the right concentration is essential, and making sure your sample preparation is accurate will contribute to reliable results.
Titration
Titration is a laboratory technique used in volumetric analysis to determine the concentration of a solution. This is done by allowing a solution of known concentration (titrant) to react with a solution of the substance being measured. In the exercise, hydrochloric acid (\(0.1 \, \text{M} \, \text{HCl}\)) serves as the titrant, reacting with sodium carbonate in the washing soda sample. The method involves adding the titrant to the analyte until the reaction reaches its endpoint, signified by a color change due to the bromocresol green indicator.

The indicator is critical in titrations. Bromocresol green, a pH indicator, changes color at the endpoint of the reaction, indicating that the titration is complete. It's essential to add the titrant slowly near the endpoint to avoid overshooting it, ensuring the reaction is complete just as the color change occurs. The volume of titrant used is then recorded and used to calculate the concentration of the analyte.

Accurate titration depends on good technique. This includes:
  • Careful measurement of the titrant and sample volumes,
  • Consistent use of the same indicator type and amount, and
  • Steady and precise addition of the titrant.
These practices help in obtaining reliable and reproducible results, crucial for evaluating the purity of the sodium carbonate and ensuring it meets the >98% purity standard.
Sample Preparation
Sample preparation is a vital aspect of quantitative analysis, ensuring that the sample is in an appropriate form for analysis. In the provided exercise, the preparation begins with the careful weighing of approximately 4 grams of washing soda. This sample is then dissolved in about 100 mL of water in a volumetric flask. It is important to wait until the solid is fully dissolved before diluting to mark with water. This ensures that the entire sample is within solution, producing accurate results during analysis.

When adapting this procedure for purer sodium carbonate (claims of >98% purity), adjustments are necessary because higher purity translates into a larger concentration of sodium carbonate in the solution. This can lead to saturation if the initial mass is too high.
To address this, reduce the mass of the sample so that it dissolves entirely without oversaturating the solution. Additionally, for purer substances, the initial and resultant solution may have a higher concentration than initially prepared, necessitating accurate dilution and potential adjustment of aliquot sizes to enable practical titration volumes. Proper sample preparation ensures effective titration and accurate analysis results.
Purity Evaluation
Evaluating the purity of sodium carbonate involves determining how close the compound is to the claimed >98% purity. This means confirming that at least 98% of the substance is indeed sodium carbonate, minimizing extraneous materials. The titration procedure in this exercise serves as a method for this evaluation.

The purity evaluation hinges on accurate measurement and titration. By calculating the volume of \(\text{HCl}\) required to react with the \(\text{Na}_2\text{CO}_3\), one can determine the amount of sodium carbonate in the sample. The key outcome of this calculation will display what percentage of the sample is actual sodium carbonate by considering the molar ratio seen in the reaction equation. This requires:
  • Accurate weighing and dissolution of the sodium carbonate,
  • Precise titration technique, and
  • Proper calculation using the titration data to deduce the percentage purity.
For evaluating commercial sodium carbonate, any deviations from the expected results may suggest impurities or experimental errors. When adapting such procedures, consider modifications that suit the purity level, ensuring accurate results that reflect the true nature of the sample.

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Most popular questions from this chapter

The exact concentration of \(\mathrm{H}_{2} \mathrm{O}_{2}\) in a solution that is nominally \(6 \%\) \(\mathrm{w} / \mathrm{v} \mathrm{H}_{2} \mathrm{O}_{2}\) is determined by a redox titration using \(\mathrm{MnO}_{4}^{-}\) as the titrant. A \(25-\mathrm{mL}\) aliquot of the sample is transferred to a \(250-\mathrm{mL}\) volumetric flask and diluted to volume with distilled water. A \(25-\mathrm{mL}\) aliquot of the diluted sample is added to an Erlenmeyer flask, diluted with \(200 \mathrm{~mL}\) of distilled water, and acidified with \(20 \mathrm{~mL}\) of \(25 \% \mathrm{v} / \mathrm{v} \mathrm{H}_{2} \mathrm{SO}_{4} .\) The resulting solution is titrated with a standard solution of \(\mathrm{KMnO}_{4}\) until a faint pink color persists for \(30 \mathrm{~s}\). The results are reported as \(\% \mathrm{w} / \mathrm{v} \mathrm{H}_{2} \mathrm{O}_{2}\). (a) Many commercially available solutions of \(\mathrm{H}_{2} \mathrm{O}_{2}\) contain an inorganic or an organic stabilizer to prevent the autodecomposition of the peroxide to \(\mathrm{H}_{2} \mathrm{O}\) and \(\mathrm{O}_{2}\). What effect does the presence of this stabilizer have on the reported \(\% \mathrm{w} / \mathrm{v} \mathrm{H}_{2} \mathrm{O}_{2}\) if it also reacts with \(\mathrm{MnO}_{4}^{-} ?\) (b) Laboratory distilled water often contains traces of dissolved organic material that may react with \(\mathrm{MnO}_{4}^{-}\). Describe a simple method to correct for this potential interference. (c) What modifications to the procedure, if any, are needed if the sample has a nominal concentration of \(30 \% \mathrm{w} / \mathrm{v} \mathrm{H}_{2} \mathrm{O}_{2}\).

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