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-Involves reacting a measured
volume of a standard solution
with a measured volume of thesolution of unknown
concentration.
-This process is carry out through
titration
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There are three practical activities associated with
titrations:1.Preparation of solutions to be used in the titration
2.Preparation of glassware to be used in the
titration
3.Performing the titration, including the recording
of burette readings
At the conclusion of a titration, calculation must
be performed using data obtained from the
titration.
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Many chemicals are impure or without
accurately supplied concentration e.g.KOH and NaOH is hygroscopic / deliquescenti.e. rapidly absorbs moisture from the
atmosphere. Moreover, these strong bases canreact with acidic oxide present in the air i.e.CO2
Strong acids are supplied in concentrated
form by manufacturers and have a viableconcentration from batch to batch
==== Therefore the amount of substance can·t
be calculated or obtained ACCURATELY!!!
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Primary Standard
-Is a stable, colourless, water-soluble
solid, readily available in high purity,
used to make a solution of knownconcentration for volumetric analysis.
* The solution is called a
µ Standard solution¶
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Criteria for a primary standard
Primary Standard must obey the following criteria
1. Obtainable in pure form (no. of moles can be
obtained)
2. Has a known formula (no. of moles can be obtained)
3. Do not absorb moisture or other chemicals in the air
i.e. stable in air. (no. of moles can be obtained)
4. Has a reasonable high molar mass (to minimizeweighing error)
5.Completely soluble in the solvent (water) at room
temperature.Exp: Anhydrous sodium carbonate & Hydrated oxalic acid
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Determine the
end point of a
titration
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-Usually there isn¶t a need to use an indicator
as there is a significant colour change
experienced by either the reductant or theoxidant ± self indicating
-Self indicating ± the ability of one of its
reactants to undergo visible colour changeduring the course of the reaction
-Example???
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1.Using wrong indicator 2.Error in rinsing of glassware
3.P
arallax error while taking the readingof burette
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If we have a analyte that has acid-base or redox properties
and is soluble but also fits into one or more of the following
categories?
Insoluble ± can¶t prepare solution
Volatile
Gaseous and in a mixture of gases
Fairly unreactive ± that is too weak to have clearly definedend-point. Exp: weak acids / bases
Then direct titration can¶t be used to determine the amount of
analyte. Back titration is the suitable method.
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Back TitrationStep 1: Excess amount and accurately known amount of
S is added to the system to react with the R (analyte). Atthe end of the reaction, R is fully reacted i.e. no more R in
the system.R + S T + V
Step 2: Titration is carried out to determine the amount of unreacted S from step 1
S + W X + Y
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In order to determine the concentration of ammonia, as % w/v, in a particular
brand of household cleaner, the following procedure was carried out:
Step 1: 10.0 mL of the household cleaner was pipetted into a volumetric
flask and the volume made up to 200 mL with water.
A 20.0 mL aliquot of the solution from the volumetric flask was transferred to
a conical flask. 20.0mL of 0.105 mol L-1 hydrochloric acid solution was then
added. The following reaction took place:
NH3 + HCl NH4Cl * for this reaction the HCl was in
excess
Step 2: To determine the surplus amount of hydrochloric acid from Step 1,
the solution remaining from Step 1 was titrated with 0.0500 mol L-1 sodium
hydroxide solution using phenolphthalein indicator to detect the end point.The average titre value obtained was 6.45 mL. The titration equation is as
follows:
NaOH + HCl NaCl + H2O
Calculating the % w/v concentration of ammonia in the cleaner