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Understanding Salt Chemistry Basics

The document discusses the preparation, separation, and purification of salts. It defines salts as compounds formed when hydrogen in an acid is replaced by a metal. Salts have many important uses including in fertilizers, batteries, and healthcare products. The document outlines methods for preparing soluble and insoluble salts, and provides examples like preparing copper (II) sulfate crystals and lead (II) sulfate crystals. It also discusses identifying cations and anions in salts using tests like reactions with sodium hydroxide or ammonia and flame tests.

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abdullah khalil
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0% found this document useful (0 votes)
49 views63 pages

Understanding Salt Chemistry Basics

The document discusses the preparation, separation, and purification of salts. It defines salts as compounds formed when hydrogen in an acid is replaced by a metal. Salts have many important uses including in fertilizers, batteries, and healthcare products. The document outlines methods for preparing soluble and insoluble salts, and provides examples like preparing copper (II) sulfate crystals and lead (II) sulfate crystals. It also discusses identifying cations and anions in salts using tests like reactions with sodium hydroxide or ammonia and flame tests.

Uploaded by

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

Salts and chemical

Analysis

Preparation, Separation
& Purification of Salts
Salts

A salt is a compound that is


formed when the hydrogen
atom in an acid is replaced by
a metal.
Preparation, Separation
& Purification of Salts

For example if we replace


the H in HCl with a
potassium atom, then the
salt potassium chloride is
formed, KCl.
Preparation, Separation
& Purification of Salts

Salts are an important


branch of chemistry due to
the varied and important
uses of this class of
compounds.
Preparation, Separation
& Purification of Salts

These uses include


fertilisers, batteries,
cleaning products,
healthcare products and
fungicides.
Preparation, Separation
& Purification of Salts

Naming salts

The name of a salt has two


parts:

The first part comes from


the metal, metal oxide
or metal carbonate used in
the reaction.
Preparation, Separation
& Purification of Salts

The second part comes


from the acid.

The name of the salt can be


determined by looking at
the reactants.
Preparation, Separation
& Purification of Salts

For example hydrochloric


acid always produces salts
that end in chloride and
contain the chloride ion, Cl–

Preparation, Separation
& Purification of Salts
Other examples:

Sodium hydroxide reacts


with hydrochloric acid to
produce sodium chloride.

Zinc oxide reacts


with sulfuric acid to
produce zinc sulfate.

Preparation, Separation
& Purification of Salts
Preparing salts

Some salts can be extracted


by mining but others need
to be prepared in the
laboratory.

Preparation, Separation
& Purification of Salts
There are two key ideas to
consider when preparing
salts:

Is the salt being


formed soluble or insoluble
in water?

Preparation, Separation
& Purification of Salts
Is there water of
crystallisation present in
the salt crystals?
Preparation, Separation
& Purification of Salts

Preparing soluble salts

Method A: adding acid to a


solid metal, base or
carbonate.
Preparation, Separation
& Purification of Salts

Method:

Add dilute acid into a


beaker and heat using a
bunsen burner flame.
Preparation, Separation
& Purification of Salts

Add the insoluble metal, base


or carbonate, a little at a time,
to the warm dilute acid and
stir until the base is in excess
(i.e. until the base stops
disappearing and a suspension
of the base forms in the acid).
Preparation, Separation
& Purification of Salts

Filter the mixture into an


evaporating basin to
remove the excess base.

Heat the solution to


evaporate water and to
make the solution
saturated.
Preparation, Separation
& Purification of Salts

Check the solution is


saturated by dipping a cold,
glass rod into the solution
and seeing if crystals form
on the end.
Preparation, Separation
& Purification of Salts

Leave the filtrate in a


warm place to dry and
crystallize. Decant excess
solution and allow crystals
to dry.
Preparation, Separation
& Purification of Salts

Preparation of pure,
Hydrated Copper (II)
Sulfate Crystals using
Method A

Acid = Dilute Sulfuric Acid


Preparation, Separation
& Purification of Salts

Insoluble base = Copper (II)


Oxide

Method:

Add dilute sulfuric acid into


a beaker and heat using a
bunsen burner flame.
Preparation, Separation
& Purification of Salts

Add copper (II) oxide


(insoluble base), a little at a
time to the warm dilute
sulfuric acid and stir until
the copper (II) oxide is in
excess (stops disappearing).
Preparation, Separation
& Purification of Salts

Filter the mixture into an


evaporating basin to
remove the excess copper
(II) oxide. Leave the filtrate
in a warm place to dry and
crystallize.
Preparation, Separation
& Purification of Salts

Decant excess solution and

blot crystals dry.

Equation of reaction:

Copper (II) Oxide + Dilute


Sulfuric Acid → Copper (II)
Sulphate + Water
Preparation, Separation
& Purification of Salts

CuO (s) + H2SO4 (aq) →


CuSO4 (s) + H2O (l)

Method B: reacting a dilute


acid and alkali
Preparation, Separation
& Purification of Salts

Method:

Use a pipette to measure


the alkali into a conical
flask and add a few drops
of indicator
(phenolphthalein or methyl
orange).
Preparation, Separation
& Purification of Salts

Add the acid into the burette


and note the starting volume.

Add the acid very slowly from


the burette to the conical flask
until the indicator changes to
appropriate colour.
Preparation, Separation
& Purification of Salts

Note and record the final


volume of acid in burette
and calculate the volume of
acid added (starting volume
of acid – final volume of
acid).
Preparation, Separation
& Purification of Salts

Add this same volume of


acid into the same volume
of alkali without the
indicator. Heat to partially
evaporate, leaving a
saturated solution.
Preparation, Separation
& Purification of Salts

Leave to crystallise decant


excess solution and allow
crystals to dry.
Extended Only

Preparing Insoluble Salts

Insoluble salts can be


prepared using a
precipitation reaction.
Preparing Insoluble Salts

The solid salt obtained is


the precipitate, thus in
order to successfully use this
method the solid salt being
formed must be insoluble in
water.

Using two soluble reactants


Preparing Insoluble Salts

Method:

Dissolve soluble salts in


water and mix together
using a stirring rod in a
beaker.
Preparing Insoluble Salts

Filter to remove precipitate


from mixture.

Wash filtrate with water to


remove traces of other
solutions. Leave in an oven
to dry.
Preparing Insoluble Salts

Preparation of Pure, Dry


Lead (II) Sulfate Crystals
using a precipitation
reaction

Soluble Salt 1 = Lead (II)


Nitrate

Soluble Salt 2 = Potassium


Sulfate
Preparing Insoluble Salts

Method:

Dissolve Lead (II) Nitrate


and Potassium Sulfate in
water and mix together
using a stirring rod in a
beaker.
Preparing Insoluble Salts

Filter to remove precipitate


from mixture.

Wash precipitate with


water to remove traces of
potassium nitrate solution.

Leave in an oven to dry.


Preparing Insoluble Salts

Equation of reaction:

Lead (II) Nitrate +


Potassium Sulfate → Lead
(II) Sulfate + Potassium
Nitrate

Pb(NO3)2 (aq) + K2SO4 (aq)


→ PbSO4 (s) + 2KNO3 (aq)
Extended Only

Selecting a Method of
Preparation

Selecting a method of
preparation. When deciding the
method of preparation, it is
important to first know
whether the salt being
produced is soluble or insoluble.
Selecting a Method of
Preparation

If it is soluble then it can be


prepared using either
method (A or B) for
preparing a soluble salt.

If it is insoluble then it must


be prepared by using
precipitation.
Identification of Cations

Metal cations in aqueous


solution can be identified by
the colour of the precipitate
they form on addition of
sodium hydroxide and
ammonia.
Identification of Cations

If only a small amount of


NaOH is used then normally
the metal-
hydroxide precipitates

In excess NaOH some of the


precipitates may dissolve.
Identification of Cations

A few drops of NaOH is added


at first and any colour changes
or precipitates formed are
noted.

Then the NaOH is added in


excess and if the reaction is
observed [Link] steps are
repeated for the test using
ammonia solution.
Identification of Cations

Analysing results

The table contains the results


for each of the cations included
in the syllabus, a precipitate is
formed from either NaOH or
aqueous ammonia then the
hydroxide is insoluble in water.
Identification of Cations

Zinc for example reacts as


such:

ZnCl2(aq) + 2NaOH(aq)
→Zn(OH)2 + 2NaCl (aq)
Identification of Cations

Ca2+ ions can be


distinguished from
Zn2+ and Al3+ as calcium
hydroxide precipitate does
not dissolve in excess NaOH
but both zinc hydroxide and
aluminium hydroxide do.
Identification of Cations

Zn2+ ions can be


distinguished from Al3+ ions
as ZnOH dissolves in excess.
aqueous ammonia but
Al(OH)3 does not.

Most transition metals


produce hydroxides with
distinctive colours.
Identification of Cations

Tests for cations

The flame test is used to


identify the metal cations
by the colour of the flame
they produce.
Identification of Cations

A small sample of the


compound is placed on
an unreactive metal wire
such as nichrome or
platinum.

The colour of the flame is


observed and used to
identify the metal.
Exam Tip

The ammonia or sodium


hydroxide solution must be
added very slowly. If it is
added too quickly and the
precipitate is soluble in
excess.
Exam Tip

Then you run the risk of


missing the formation of
the initial precipitate,
which dissolves as quickly as
it forms if excess solution is
[Link] sure to distinguish
between the term
“colourless” and “clear”.
Exam Tip

A solution that loses its


colour has become
colourless. A clear solution is
one that you can see

through such as water.


Solutions can be clear and
have colour eg. dilute
copper sulphate.
Identification of Anions
Exam Tip

When it comes to
qualitative inorganic
analysis, always remember
that there will be a test for
the metal cation part of
the molecule and another
test for the anion part.
Identification of Gases

Several tests for anions and


cations produce gases which
then need to be tested.

The table below indicates


the tests for the gases
included in the syllabus.
Exam Tip

It is easy to confuse the


tests for hydrogen and
oxygen. Try to remember
that a ligHted splint has a
H for Hydrogen, while a
glOwing splint has an O for
Oxygen.

Common questions

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The preparation of hydrated Copper (II) Sulfate crystals using Method A involves adding dilute sulfuric acid to a beaker and heating it with a Bunsen burner. Copper (II) oxide is then added gradually until it is in excess. The mixture is filtered to remove the excess copper (II) oxide, leaving behind the copper (II) sulfate solution. This solution is allowed to cool and crystallise, forming pure hydrated Copper (II) Sulfate crystals. Solubility is a critical factor as it determines the method of preparation; soluble salts are prepared through reactions involving a dilute acid with bases or metals, while insoluble salts require precipitation methods .

A misunderstanding between 'colourless' and 'clear' solutions can lead to inaccurate interpretation of results in qualitative inorganic analysis. 'Colourless' denotes the absence of color, while 'clear' refers to transparency. Mistaking one for the other may cause errors in identifying endpoint reactions, particularly in titrations or precipitate tests, where visual cues are vital for determination. Such confusion can ultimately compromise the reliability of the analysis .

To ensure complete removal of impurities in salt synthesis, the mixture is typically filtered to separate solid impurities, followed by thorough washing with distilled water. The resultant filtrate containing the dissolved salt is then evaporated slowly to form crystals, which are further decanted to remove remaining solution. Finally, the crystals are dried completely in an oven. Each step is designed to remove traces of reactants or secondary products, ensuring the purity of the final crystal .

Precipitation reactions are used to prepare insoluble salts by mixing two soluble salts in aqueous solution to form a precipitate. For instance, mixing Lead (II) Nitrate and Potassium Sulfate results in the formation of insoluble Lead (II) Sulfate. The process involves dissolving the salts, stirring the mixture to form a precipitate, filtering, washing, and drying the solid. The reaction is solely employed for insoluble salts, as they precipitate out of solution, allowing easy separation .

Challenges in using precipitation reactions include ensuring complete precipitation, avoiding the formation of impurities, and achieving uniform particle size. These issues can lead to difficulties in filtration and purification. Overcoming these involves optimizing conditions such as temperature and concentration, controlling the rate of mixing, and thorough washing of the precipitate. Additionally, advanced techniques like seeding can promote uniform crystallization and minimize impurities during the drying phase .

The slow addition method for sodium hydroxide or ammonia is crucial in cation identification to observe the correct sequence of reactions—initial precipitate formation and subsequent dissolution in excess if applicable. This precision prevents missing intermediate states and ensures clear differentiation between cations, such as distinguishing Zn2+ from Al3+ based on solubility differences in excess reagent. Rapid addition could dissolve a transient precipitate if soluble in excess, leading to incorrect conclusions .

Preparing soluble salts using a dilute acid and alkali method can be advantageous due to its simplicity and ability to produce high-purity salts without requiring solid reactants. This method allows precise control over the stoichiometry through titration, ensuring complete reaction with minimal waste. It is particularly useful for preparing salts used in sensitive applications where purity is paramount, and the absence of excess solid residue makes the purification process easier .

The naming convention of salts is derived from the reactants used in their formation. The first part of a salt's name comes from the metal, metal oxide, or metal carbonate involved in the reaction. The second part of the name is based on the acid used; for example, hydrochloric acid leads to chloride salts. This systematic approach allows the identification of both the metal ion and the corresponding anion based on the reactants .

Identifying the solubility of a salt is crucial before choosing its preparation method because it determines whether the salt should be prepared using a precipitation method or a reaction involving a dilute acid. Soluble salts can be formed by reacting an acid with a metal, base, or carbonate, while insoluble salts require precipitation methods using two soluble reactants. This distinction ensures the appropriate method is used to efficiently produce the desired salt .

Metal cation identification is performed by adding a few drops of sodium hydroxide or ammonia to an aqueous solution of the metal, observing any immediate precipitate or color change, and then adding an excess of the reagent to check for dissolving. Zinc, for example, forms a white precipitate with NaOH which dissolves in excess ammonia, distinguishing it from aluminum, whose hydroxide does not dissolve with excess ammonia. This methodology is essential in analytical chemistry to determine the specific cations in a sample, aiding in substance identification and quality control .

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