Analysis Stoichiometry Gordon Watson Chemistry Department Kelso High

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Analysis & Stoichiometry Gordon Watson Chemistry Department, Kelso High School Adv Higher Unit 2

Analysis & Stoichiometry Gordon Watson Chemistry Department, Kelso High School Adv Higher Unit 2 Topic 1

Introduction This topic explores various aspects of Chemical Analysis, leading to an appreciation of

Introduction This topic explores various aspects of Chemical Analysis, leading to an appreciation of the importance of Stoichiometry in chemical reactions.

Stoichiometry involves the understanding of numerical relationships between reacting substances. One methane molecule CH

Stoichiometry involves the understanding of numerical relationships between reacting substances. One methane molecule CH 4 Two oxygen molecules 2 One carbon dioxide molecule CO 2 Two water molecules 2 H 2 O

The Molar relationships , in turn, allow us to establish measurable relationships between reacting

The Molar relationships , in turn, allow us to establish measurable relationships between reacting substances. 1 moles 16 g 32 g 1 moles 44 g 25 l 50 l 25 l 2 2 36 g

Volumetric Analysis This method of chemical analysis involves accurately measured volumes. Instruments such as

Volumetric Analysis This method of chemical analysis involves accurately measured volumes. Instruments such as pipettes and burettes are used to measure volumes accurately Solutions of unknown concentration are titrated against a solution of known concentration - a primary standard solution or standard solution

Gravimetric Analysis This method of analysis involves accurate weighing. Access to an Analytical Balance,

Gravimetric Analysis This method of analysis involves accurate weighing. Access to an Analytical Balance, capable of reading to 2 decimal places at least, is essential. The analysis will usually involve the production of a suitable precipitate: very low solubility high molecular mass Stoichiometry 1 mole = gfm

Primary standard A Primary standard is a substance that has the following characteristics: •

Primary standard A Primary standard is a substance that has the following characteristics: • a high purity (> 99. 9%) • is stable in air and in solution • a reasonably high formula mass • is reasonably soluble Suitable substances include: Potassium hydrogen pthalate (acid) and sodium carbonate

Standard Solution Stoichiometry n = mass / gfm C = n / V

Standard Solution Stoichiometry n = mass / gfm C = n / V

Standard Solution A Standard Solution is one whose concentration has been established by titrating

Standard Solution A Standard Solution is one whose concentration has been established by titrating against a Primary Standard …. . or against another Standard Solution whose concentration had been established by titrating against a Primary Standard …. . Stoichiometry C 1 V 1 p 1 = C 2 V 2 p 2

Dilutions Once prepared, standard solutions can be used a stock solutions and further diluted

Dilutions Once prepared, standard solutions can be used a stock solutions and further diluted solutions can be made. Stoichiometry C 1 V 1 = C 2 V 2

Titrations Acid-Base Titrations - neutralisation reactions requiring an indicator to detect the end-point Na.

Titrations Acid-Base Titrations - neutralisation reactions requiring an indicator to detect the end-point Na. OH(aq) + CH 3 COOH(aq) → Na. CH 3 COO(aq) + H 2 O(l) Redox Titrations - based on redox reactions, often self-indicating due to strong colours, e. g. KMn. O 4 -(aq) + 8 H+(aq) → Mn 2+(aq) + 4 H 2 O(l) 2 I-(aq) → I 2(aq) + 2 e- Complexometric Titrations - based on ligand reactions, requiring an indicator that can be replaced [Ni(In)](aq) + EDTA 4 -(aq) → [Ni(EDTA)]2 -(aq) + In

Acid-Base Titrations

Acid-Base Titrations

Equivalence point The equivalence point is when the reaction is just completed For a

Equivalence point The equivalence point is when the reaction is just completed For a titration between a strong acid (e. g HCl) and a strong base (e. g Na. OH) the equivalence point will be when p. H = 7. However, not all indicators will complete their colour change at this point so endpoint observed may be different.

Indicators change colour over a p. H range.

Indicators change colour over a p. H range.

End point In this case both indicators would change just before or just after

End point In this case both indicators would change just before or just after the equivalence point In this case one indicator would change just after the equivalence point, but the other would be no good.

Redox Titrations An excess of Mn. O 4 - must be added to detect

Redox Titrations An excess of Mn. O 4 - must be added to detect the end-point. Fortunately Mn. O 4 - is so strongly coloured that end-point is very close to equivalence point.

Complexometric Titration Murexide indicator forms a yellow 2+ green complex with Ni ions. EDTA

Complexometric Titration Murexide indicator forms a yellow 2+ green complex with Ni ions. EDTA is added 2+ and starts to complex with any free Ni ions first. Finally, EDTA will replace the murexide molecules and the colour of free murexide - purple - will be produced. Any decision about the end-point relies on there being enough free murexide to produce a distinct colour change. What about the equivalence point?

Difficult Titrations The weaker the acid, the smaller the region of rapid p. H

Difficult Titrations The weaker the acid, the smaller the region of rapid p. H change which includes the equivalence point. For very weak acids, it is impossible to detect an endpoint close to the equivalence point

Back Titration The solution to this problem is a technique known as a back

Back Titration The solution to this problem is a technique known as a back titration. A carefully measured volume of base would be added to ensure complete reaction of the weak acid. A strong acid would then be used to determine the excess base left over. The amount of base which reacted with the weak acid can now be calculated and, hence, the amount of weak acid present originally.

Analysis & Stoichiometry End of Topic 1

Analysis & Stoichiometry End of Topic 1