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Chem p1 (20232024)

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NOTES
Index
Part 1

The periodic table - Atomic Structure.

States of matter.
(10 -22)

Chemical formula of compound.
(23-28)

Bonding.
(29 -34)

Material structure.
(35-42)

Elements.
(43-61)

Colours
.
(62 -63)

Types of Chemical Reaction
(64 -79)

Energy and Chemistry.
(74-80)

Acids and Alkalis.
(81-90)

Salt Preparation.
(91 - 107)

Mixtures Separation and purification.

practical work
(1)
(102 -108)
(109 - 117 )
Atomic Structure
 Matter is anything that has mass and takes up space (volume).
 Chemistry is the study of how matter behaves and how one kind
of substance can be changed into another.
 Matter consists of molecules.
 A molecule is a group of atoms held together by covalent bonds .


 A molecule in turn consists of atoms.
 An atom is the smallest particle of an element that takes part in a
chemical reaction without being changed.
Matter can be classified into pure substances and mixtures.
More than one substance mixed in any ratio.
impurities
Examples: air, sea water and petroleum.
An element is a substance that consists of one type of atoms that can not be
splitted into simpler substances.
bonded together.
Examples: water, Carbon dioxide, Sodium chloride.
The periodic table - Atomic Structure.
Amani Hamdi
Page 1
Each element has a symbol, for example:
Aluminum
Phosphorous
Carbon
Calcium
Al
P
C
Ca
Sulfur
S
Potassium K
Chlorine
Cl
Iron
Fe
Sodium
Silicon
Copper
Nitrogen
Na
Si
Cu
N
 Elements can be classified into metals and non-metals.
 Elements are monoatomic, diatomic and polyatomic.
Elements
Monoatomic
The molecule of the
element is formed of
one atom.
Examples: Na, K, Al, Ca,
and all noble gases.
Diatomic
The molecule consists of two
atoms.
Examples: H2, N2, O2 and
halogens (F2, Cl2, Br2, I2 and
At2)
Polyatomic
The molecule consists of
more than two atoms.
Examples: P4 , S8
 A Compound is a substance that is formed of different elements
that combine together in a fixed ratio by chemical bonds.
 Although there is a limited number of elements, there are millions
of compounds.
The periodic table - Atomic Structure.
Amani Hamdi
Page 2
Atomic Structure
 An atom is the smallest particle of a
substance that can share in a chemical
reaction without being changed.
 It consists of a nucleus, and a cloud of
particles called electrons that rotate
around the nucleus.
6 electrons
outside
nucleus
nucleus
contains 6
protons and
6 neutrons
 The nucleus is a cluster of two sorts of sub- particles, protons and
neutrons. All the particles in an atom are very light. Their mass is
measured in atomic mass units (a.m.u), rather than grams. Protons and
electrons also have an electric charge.
Particle in atom
Proton
Neutron
Electron
Relative mass
1 a.m.u
1 a.m.u
1/1843 ~ 1/2000 a.m.u
Relative charge
Positive change (+1)
zero
Negative change (-1)
 The protons are positively charged, the electrons are negative and the
neutrons are neutral (have no charge).
 The electrons rotate around the nucleus in energy levels (electron shells).
 Each shell can hold a limited number of electrons.
The 1st shell
The 2nd shell
The 3rd shell
2 electrons
8 electrons
18 electrons
 Atomic number (Proton number):
It is the number of protons in the nucleus of an atom.
 Mass number ( nucleon number) :
It is the sum of protons and neutrons in the nucleus of an atom.
 The electrons in an atom have almost no mass. So the mass of an atom is
nearly due to its protons and neutrons
The periodic table - Atomic Structure.
Page 3
Amani Hamdi
Shorthand form of an atom:
An atom can be described in a short way, using its symbol, its proton
number and its mass number in a certain order as the following:
Z
A
The proton number
Symbol of element
The mass number
Note that:
 The atomic no. = the no. of protons = the no. of electrons in an atom.
 The mass number = no. of protons + no. of neutrons.
 So the no. of neutrons = the mass no. – Atomic no.
Example:
11
23
Na
This is a Sodium atom.
That has 11 protons, 11 electrons and 12 neutrons (23-11=12)
Valency:
 Nobel gases are stable or uncreative because they have completely filled
outermost shell.
 They have eight electrons in their outermost shell except Helium that has
2 electrons (as it has only 1 shell that is completed by only 2 electrons).
 All atoms tend to have the same electronic structure as noble gases. This
can be done by losing, gaining or sharing electrons from the outermost
shell of the atom during a chemical reaction.
 The number of electrons lost, gained or shared by an atom is called the
valency of an element.
 Metals tend to lose the outermost shell electrons.
 Non-metals tend to gain or share electrons.
 Transition elements have more than one valency.
The periodic table - Atomic Structure.
Page 4
Amani Hamdi
The following table shows the Valencies of some elements:
Element
Sodium
Chlorine
Magnesium
Oxygen
Aluminum
Nitrogen
Carbon
Silicon
Symbol
Electronic
configuration
11Na
2, 8, 1
2, 8, 7
2, 8, 2
2, 6
Change of
formed ion
Mono valent
1+
Mono valent
1Divalent
2+
Divalent
2-
2, 8 , 3
2,5
2, 4
2, 8, 4
Trivalent
Trivalent
Tetravalent
Tetravalent
17Cl
12Mg
8O
13Al
7N
6C
14Si
Valency
3+
3-
Notes
loses 1é
gains 1 é
loses 2 é
gains 2é
loses 3é
gains 3é
Tend to
share 4é
 Atoms of metals have 1, 2 or 3 electrons in the outermost shell except for
Hydrogen, Helium and Boron, they are non-metals.
 Atoms of non-metal have 4, 5, 6 or 7 é in their outermost shell.
 Nobel gases have completely filled outermost shell (atoms of noble gases
have 8 electrons in the outermost shell except for Helium it has only 2
electrons), so they have a valency of zero.
 Metals tend to lose electrons.
 Non-metals that have 4 electrons tend to share electrons.
 Non-metals that have 5,6 or 7 electrons tend to gain or share electrons.
The periodic table - Atomic Structure.
Page 5
Group 0
Group 7
Group 6
Group 5
Transition Metals
He
3+ 4± 3- 2- 1- 0
Group 4
Group 2
Period 3
1+ 2+
Group 1
Period 2
H
Valency
Group 3
Period 1
Amani Hamdi
Isotopes
Isotopes: atoms of the same element which have the same proton
number but different nucleon number.
Examples:
H- 1 , H -2 , H -3
Cl- 35 , Cl-37
U -235 , U -238
 The atoms of the isotopes have the same number of protons but
different numbers of neutrons in their nuclei.
 Isotopes of an element have the same chemical properties
because they have the same electron structure and so same
olinumber of electrons in the outermost shell.
The relative atomic mass (Ar) is the average mass of naturally
occurring atoms of the same element on a scale where carbon-12
atom has a mass of exactly 12 units.
The relative atomic mass, Ar, of an element is calculated from:
the mass numbers of its isotopes
the abundance of these isotopes
The periodic table - Atomic Structure.
Amani Hamdi
Page 6
For e.g : Chlorine
Chlorine naturally exists as two isotopes, Cl (chlorine-35)
and Cl (chlorine-37). The abundance of chlorine-35 is 75%
and the abundance of chlorine-37 is 25%. In other words, in
every 100 chlorine atoms, 75 atoms have a mass number of
35, and 25 atoms have a mass number of 37.
To calculate the relative atomic mass, Ar, of chlorine:
Ar=total mass of atoms / total number of atoms
= (35 x 75) + (37 x 25)
(75 + 25 )
Ar =
2625 + 925
100
=
3550
100
Ar=35.5 (to 1 decimal place)
Notice that the answer is closer to 35 than it is to 37. This is
because the chlorine-35 isotope is much more abundant than
the chlorine-37 isotope.
Amani Hamdi

The periodic table - Atomic Structure.
Page 7
The Periodic Table
Scientists put all the elements into groups according to their atomic number in
an ascending order as follows.
 Hydrogen comes first, as its proton number (atomic no.) is 1.
 The table has eight vertical groups of elements, plus a block of transition
metals.
 The last group is the group zero. Their atoms have completely filled
outermost shells.
Some groups have special names:
Group 1 is called Alkali Metals.
Group 2 is called Alkaline Earth Metals.
Group 7 is called Halogens.
Group 0 is called Noble gases.
 Transition metals lie in the middle of the periodic table between group 2
and 3 beginning from the 4th period. They include most hard and dense
metals.
 The horizontal rows in the periodic table are called periods.
 There are several trends as you move across the period, for example; the
elements go from metals to non-metals.
 Some substances between metals and non-metals like Silicon are like
metals in some ways and non-metals in other ways. They are called
Metalloids.
 Hydrogen stands on its own in the periodic table. This is because it has one
outermost electron, like the group 1 metals, but unlike them it is a gas and
it usually reacts like non-metals.
 Not all elements occur naturally, some are artificial (synthesized by
scientists) during nuclear reactions. Most of these elements lie at the
bottom block of the periodic table. All isotopes of artificial elements are
radioactive. This means their atoms have unstable nuclei which break
down giving out radiation.
The periodic table - Atomic Structure.
Page 8
Amani Hamdi
The Periodic Table of Elements
Group
I
III
II
Key
3
4
atomic number
IV
V
VI
VII
VIII
1
2
H
He
hydrogen
helium
1
4
5
6
7
8
9
10
Li
Be
atomic symbol
B
C
N
O
F
Ne
lithium
beryllium
Name
boron
carbon
nitrogen
oxygen
fluorine
neon
7
9
relative atomic mass
11
12
14
16
19
20
11
12
13
14
15
16
17
18
Na
Mg
Al
Si
P
S
Cl
Ar
sodium
magnesium
aluminium
silicon
phosphorus
sulfur
chlorine
argon
23
24
27
28
31
32
35.5
40
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
K
Ca
Sc
Ti
V
Cr
Mn
Fe
Co
Ni
Cu
Zn
Ga
Ge
As
Se
Br
Kr
potassium
calcium
scandium
titanium
vanadium
chromium
manganese
iron
cobalt
nickel
copper
Zinc
gallium
germanium
arsenic
selenium
bromine
krypton
39
40
45
48
51
52
55
56
59
59
64
65
70
73
75
79
80
84
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
Rb
Sr
Y
Zr
Nb
Mo
Tc
Ru
Rh
Pd
Ag
Cd
In
Sn
Sb
Te
I
Xe
rubidium
strontium
yttrium
zirconium
niobium
molybdenum
technetium
ruthenium
rhodium
palladium
silver
cadmium
indium
tin
antimony
tellurium
iodine
xenon
85
88
89
91
93
96
–
101
103
106
108
112
115
119
122
128
127
131
55
56
57–71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
Cs
Ba
lanthanoids
Hf
Ta
W
Re
Os
Ir
Pt
Au
Hg
Tl
Pb
Bi
Po
At
Rn
caesium
barium
hafnium
tantalum
tungsten
rhenium
osmium
iridium
platinum
gold
mercury
thallium
lead
bismuth
polonium
astatine
radon
133
137
178
181
184
186
190
192
195
197
201
204
207
209
–
–
–
87
88
89–103
104
105
106
107
108
109
110
111
112
actinoids
114
116
Fr
Ra
Rf
Db
Sg
Bh
Hs
Mt
Ds
Rg
Cn
Fl
Lv
francium
radium
rutherfordium
dubnium
seaborgium
bohrium
hassium
meitnerium
darmstadtium
roentgenium
copernicium
flerovium
livermorium
–
–
–
–
–
–
–
–
–
–
–
–
–
lanthanoids
actinoids
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
La
Ce
Pr
Nd
Pm
Sm
Eu
Gd
Tb
Dy
Ho
Er
Tm
Yb
Lu
lanthanum
cerium
praseodymium
neodymium
promethium
samarium
europium
gadolinium
terbium
dysprosium
holmium
erbium
thulium
ytterbium
lutetium
139
140
141
144
–
150
152
157
159
163
165
167
169
173
175
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
Ac
Th
Pa
U
Np
Pu
Am
Cm
Bk
Cf
Es
Fm
Md
No
Lr
actinium
thorium
protactinium
uranium
neptunium
plutonium
americium
curium
berkelium
californium
einsteinium
fermium
mendelevium
nobelium
lawrencium
–
232
231
238
–
–
–
–
–
–
–
–
–
–
–
The volume of one mole of any gas is 24 dm 3 at room temperature and pressure (r.t.p.).
Page 9
States of matter
 There are three physical states of matter
Solid, liquid and gas.
 The individual particles of the substance are the same in each
state. It is their arrangement that is different.
Physical State
Volume
Density
Shape
Fluidity
Solid
Fixed volume
High
Definite shape
Doesn’t flow
Moderate to
high
No definite
shape ,takes
the shape of
the container
Flows easily
Low
No definite
shape, takes
the shape of
the container
Flows easily
Liquid
Fixed volume
Gas
No Fixed
volume
expands to fill
the container
Note: liquids and gases are called fluids.
States of Matter
Amani Hamdi
Page 10
State
Separation of
particles
Solid
Closely
packed
Liquid
Gas
Arrangement of
particles
Motion of particles
Regular
Vibration about fixed
point.
Fairly closely
packed
Random
Move about and slide past
each other.
Far apart,
Random
Move about very fast in
random motion.
 The volume of a gas at a fixed temperature can be easily
reduced by increasing the pressure on the gas. They are easily
compressed.
 Liquids are only slightly compressible, and the volume of a solid is
unchanged by changing the pressure.
 Particles of gases collide with each other and with the sides of the container
(This is how pressure is created inside a sealed container )
States of Matter
Amani Hamdi
Page 11
Melting
Solid
Heat
Energy"
Liquid
"by gainig
Heat
Energy"
Freezing
by losing heat
by losing heat
Solid
Sublimation
Solid
Melting: is the change of a substance from solid state to liquid state.
Melting point: is the temperature at which a solid begins to melt.
The melting point is the same value as the freezing point. For example,
the melting point and freezing point of pure water takes place at 0oC.
States of Matter
Amani Hamdi
Page 12
Sublimation: is the direct change from solid to gas without passing
through liquid state.
Few solids can sublime such as, dry ice (solid carbon dioxide) and iodine
sublimes producing a purple vapour, then solidifies again on cold
surface to return back a dark grey solid.
 If a liquid is left with its surface exposed to the air, it evaporates.
Evaporation: is the process in which a liquid changes into gas.
Evaporation takes place from the surface of the liquid. The larger the
surface area, the faster the liquid evaporates.
The warmer the liquid is, the faster it evaporates. So evaporation is
affected by surface area and temperature.
At a certain temperature the liquid becomes hot enough for a gas to
form within the liquid and not just on the surface. Bubbles of gas
appear inside the liquid. This process is known as boiling.
Boiling is a condition under which gas bubbles are able to form within a
liquid and gas molecules escape from the body of a liquid, not just
from its surface.
Boiling point: the temperature at which liquid boils, when the pressure
of gas created above the liquid equals atmospheric pressure.
A volatile liquid is one which evaporates easily and has a relatively low
boiling point. Ethanol (boiling point 78°C) is more volatile than water
(boiling point 100°C).
States of Matter
Amani Hamdi
Page 13
Evaporation
Boiling
it occurs over a range of
temperatures
it occurs only at the surface of
liquids
does not produce bubbles
occurs at specific temperature
known as boiling point
takes place throughout the bulk
of the liquid.
produces lots of bubbles
 The reverse of evaporation is Condensation.
Condensation: is the change of a vapour or a gas into a liquid.


Condensation is usually brought about by cooling. It is possible at
normal temperature to condense a gas into a liquid by increasing
pressure, without cooling.
Pure substances:
A pure substance consists of only one substance. There is no
contaminating impurities.
A pure substance melts and boils at definite temperatures.
The melting point and boiling point can be used to test for purity of
a substance, also used to check the identity of an unknown.
Amani Hamdi
States of Matter
Page 14
A substance’s melting point and boiling point in relation to room
temperature (taken as 20°C) determines whether it is usually seen as a
solid, liquid or a gas. (State of matter)
 If the melting point is below 20°C and the boiling point is above 20°C,
the substance will be a liquid at room temperature.
 If the melting point is above room temperature the substance is a
solid.
 If the boiling point is below room temperature, the substance will be
a gas at room temperature.
The melting points of some common chemical substances:
Physical state at
room
Substance
temperature(20◦C)
Oxygen
Gas
Nitrogen
Gas
Ethanol(alcohol)
liquid
Water
liquid
Sulfur
Solid
Common
salt(Sodium
Solid
Chloride)
Copper
Solid
Carbon dioxide
Gas
Melting
point/◦C
Boiling
point/◦C
-219
-210
-117
0
115
-183
-196
78
100
444
801
1465
1083
-78
2600
(sublimes)
States of Matter
Amani Hamdi
Page 15
The figure at the right shows how the temperature changes when a
sample of the solid Naphthalene (a single pure substance) is heated
steadily.
-The solid melts sharp at 80°C. While the solid is melting the temperature
stops rising. It will begin to rise again when all the Naphthalene has
melted.
-If you continue to heat the liquid until its boiling point, the temperature
stays the same until all the liquid has boiled.


heating curve for wax, which is a mixture of substances,
-The
shows the solid wax melting over a range of temperatures.
Amani Hamdi
States of Matter
Page 16
Kinetic theory
 Thermal energy (heat energy) which is converted into kinetic
energy . This is basic of kinetic theory of matter
 Heating a solid causes its particles to vibrate more and as
the temperature increases , they vibrate so much that the
solid expands , until the structure breaks and the solid melts
 On further heating , the liquid substance expands more and
some particles at the surface gain sufficient energy to
overcome the intermolecular forces and evaporate .


 when the boiling point temperature is reached , all the
particles gain enough energy to escape and the liquid boils.
 These changes in state can be shown on a graph called a
heating curve .
Amani Hamdi
States of Matter
Page 17
 cooling down a gas has the reverse effect and this would be
called a cooling curve


 when the gas is heated , the particles lose thermal energy so
the kinetic energy decreases and the particles slow down.
States of Matter
Amani Hamdi
Page 18
Diffusion in fluids
The idea that fluids (liquids and gases) are
made up of moving particles helps us to
explain processes involving diffusion.
-Dissolving Potassium Manganate (VII) crystals
is placed at the bottom of a dish of water. It is
then left to stand. At first the water around
the crystals becomes purple as the solid
diffuses. Particles move off the surface of the crystal into the water.
The crystal dissolves completely and the whole solution becomes
purple. The particles from the solid become evenly spread through the
water.
-The spreading of the solute particles throughout the liquid is an
example of diffusion.
-Diffusion in solution is also important when the solute is a gas. This is
important in breathing. Diffusion contributes to the movement of
oxygen from the lungs to the blood, and of carbon dioxide from the
blood to the lungs.
States of Matter
Amani Hamdi
Page 19
Diffusion of gases
-A few drops of liquid bromine are put
into a gas jar and covered with another
gas jar as shown. After short time the jar
becomes full of brown gas.
 Bromine gains energy from the surrounding
 The intermolcular forces between
particles of liquid bromine get weaker .
 Bromine Vaporizes .
 Particles of bromine and air collide with
each other .
 Bromine diffuses from the area of high
concentration to that of low concentration .
Definition of Diffusion:
Is the process by which different fluids mix as a result of
random motion of their particles.
 Diffusion involves the movement of particles from a region of higher
concentration towards a region of lower concentration.
 Diffusion does not take place in solids.
 Diffusion in liquids is much slower than in gases.
 Not all the gases diffuse at the same rate.
States of Matter
Amani Hamdi
Page 20
-The Ammonia and the Hydrogen chloride acid fumes react when they meet
producing a white smoke ring of Ammonium Chloride.
HCl(g) + NH3(g)
NH4Cl(s)
-The fact that the ring is not
formed halfway along the tube
shows that ammonia is a lighter
molecule than hydrogen chloride
acid fumes as the ring is formed
nearer to HCl rather than NH3.
-To show which gas is lighter, we have to calculate the relative
molecular mass (RMM or Mr) of each molecule which is the sum of the
atomic mass of each atom.
RMM of HCl = 1 + 35.5 = 36.5
RMM of NH3 = 14 + (3 x 1) = 17
NH3 has less RMM than HCl, so Ammonia diffuses at faster rate.
States of Matter
Amani Hamdi
Page 21
-The speed of gas atoms or molecules are high. These particles collide
very frequently with other particles in the air (many millions of
collisions per second). So their path is not direct.
See the figure at the right.
-These very frequent collisions slow down the overall rate of diffusion
from one place to another.
-The amount of individual gas molecules or atoms in the air can not be
seen as the particles are too small.
N .B .
 Heavier particles move more slowly than lighter particles at the same
temperature. Larger molecules diffuse more slowly than smaller
molecules.
 The pressure of a gas is the result of collisions of the fast-moving
particles with the walls of the container.
 The average speed of the particles increases with an increase in
temperature.
States of Matter
Amani Hamdi
Page 22
Chemical Formula
Formula of ionic compounds:
 Ionic compounds are formed between metal atoms and
non-metal atoms.
 Metal atoms form positive ions (cations) by losing electrons.
 Non – metal atoms form negative ions (anions) by gaining
electrons.
 The positive and negative ions attract each other forming an ionic
bond.
 The overall structure must be neutral i.e. positive and negative
charges must balance each other.
Examples:
Chemical formula of Magnesium Chloride
The ions present: Mg2+ ClClTotal charge:
2+
2-
This is why the formula is written as MgCl2
 The size of the charge on an ion is a measure of its valency.
Amani Hamdi
Chemical Formula
Page 23
Ionic Compounds
Binary
Polyatomic
Formula of binary ionic componds :
Examples :
Formula of Aluminum Oxide
 Write down the correct symbol.
Al
 Write down the charges of the ions.
 Reverse the Valencies and skip the charges.
O
Al2O3
Formula of Calcium Oxide
 Write down the correct symbol.
Ca
 Write down the charges of the ions.
 Reverse the Valencies and skip the charges.
O
Ca2O2
Formula of Manganese (IV) Oxide
CaO
Simplify
 Write down the correct symbol.
Mn
 Write down the charges of the ions.
 Reverse the Valencies and skip the charges.
O
Mn2O4
MnO2
Simplify
Amani Hamdi
Chemical Formula
Page 24
Formula of Iron (III) Oxide
 Write down the correct symbol.
Fe
 Write down the charges of the ions.
 Reverse the Valencies and skip the charges.
O
Fe2O3
Formula of Iron (II) Oxide
 Write down the correct symbol.
Fe
 Write down the charges of the ions.
2+
 Reverse the Valencies and skip the charges.
O
2Fe2O2
Simplify
N.B.Transition elements have more than one valency.
Formula of ionic compounds containing polyatomic ions:
 Follow the same rules to write the formula.
 You have to study and memorize the formula and the charges
of the polyatomic ions.
Monovalent Radicals
Divalent
Radicals
Hydroxide(OH-)
Trivalent Radicals
Carbonate(CO3-2)
Nitrate(NO3-)
Nitrite(NO2-)
Sulfate(SO4-2)
-
Hydrogen Carbonate(HCO3 )
Ammonium(NH4+)
Phosphate(PO4-3)
Sulfite(SO3-2)
Amani Hamdi
Chemical Formula
Page 25
Examples:
Formula of Sodium Carbonate
 Write down the correct symbol.
Na
 Write down the charges of the ions.
1+
 Reverse the Valencies and skip the charges.
CO3
Na2CO3
Formula of Ammonium Phosphate
 Write down the correct symbol.
NH4
PO4
 Write down the charges of the ions.
 Reverse the Valencies and skip the charges.
(NH4)3PO4
Naming Ionic Compounds
 The positive part (metal ion) is the prefix.
 The negative part (non-metal ion or the negative polyatomic ion)
is the suffix.
 For non-metal ions, the suffix is ide e.g.Calcium Chloride, CaCl2
 For negative polyatomic ions, the suffix is either ite or ate
E.g. Sodium Nitrite, NaNO2
Sodium Nitrate, NaNO3
Hint: ite has less oxygen than ate.
 Roman figures are used to indicate the Valencies of transition
metals, as they have more than one valency.
E.g. Iron(II)Oxide, FeO
Iron(III)Oxide, Fe2O3
Amani Hamdi
Chemical Formula
Page 26
Naming Covalent Compounds




Covalent compounds are formed between non-metal atoms.
The prefix is the name of the first element.
The suffix is the name of the second element, ends in ide.
Prefixes like (Mono,Di,Tri…….) are used to indicate the number of
atoms of each element.
 Mono is not used for the first element
e.g. NO2
Nitrogen dioxide, i.e. we do not say mono
Nitrogen dioxide.
 When the addition of the Greek prefix places two vowels adjacent
to one another, the “a” (or the “o”) at the end of the Greek prefix
is usually dropped; e.g., “nonaoxide” would be written as
“nonoxide”, and “monooxide”would be written as “monoxide”.
The “I” at the end of the prefixes “di-“ and “tri” are never
dropped.
Prefix
MonoDiTriTetra
Penta-
Number
Indicated
1
2
3
4
5
Prefix
HexaHeptaOctaNonaDeca-
Number
Indicated
6
7
8
9
10
Amani Hamdi
Chemical Formula
Page 27
Writing covalent compounds from their names:
Carbon tetrachloride: CCl4
Dinitrogen tetroxide: N2O4
Writing covalent names from their formulas:
I4O10
Tetraiodinedecoxide
BrCl3
Bromine trichloride
Complete the following table:
Formula
N2F6
CO2
Name
Dinitrogen hexafluoride
Silicon tetrafluoride
CBr4
Nitrogen trichloride
P 2S 3
Carbon monoxide
NO2
Carbon tetrachloride
PCl3
Amani Hamdi
Chemical Formula
Page 28
Bonding
 Atoms combine with other atoms to be able to achieve a stable
arrangement of electrons like inert gases that have completely filled
outermost shell ( Octet rule).
 Atoms combine by Ionic bonds or Covalent bonds

Ionic bonds
 Ionic bond is formed between metal and non-metal atoms.
 A metal atom loses one or more electrons from its outer most shell
forming a Positive ion
.
 A non-metal atom gains one or more electrons forming a negative ion 
 Electrostatic attraction takes place between the +ve and –ve ions forming
an ionic compound with an ionic bond.
Ionic bonding is the strong electrostatic attraction force between oppositely charged ions.
Examples:
1. Formation of Sodium Chloride (NaCl)
Bonding
Amani Hamdi
Page 29
2. Formation of Magnesium Fluoride (MgF2)
Covalent bonds
Covalent bonds take place between non-metal atoms by sharing electrons.
Covalent bonding is a Chemical bonding formed by the sharing one or more pairs of
electrons between two atoms.
Covalent bonds
Single covalent
bond
A covalent bond
that is formed by
sharing two
electrons, one
from each nonmetal atom.
Double covalent
bond
A covalent bond
that is formed by
sharing four
electrons, two from
each non-metal
atom.
Bonding
Triple covalent
bond
A covalent bond that
is formed by sharing
six electrons, three
from each non-metal
atom.
Amani Hamdi
Page 30
Examples for single covalent compounds:
C +
Atomic no. 6
1. A Methane molecule CH4
4H
1
- Electronic 2,4
configuration
H
H
H x C xH
H
H
2. A water molecule H2O
oX
O
xH
x
x
H
H
Atomic no. 1
- Electronic 1
configuration
xx
H
x
H
oX
Hx
xx
O
H
8
2,6
1
1
O
x
3. A Hydrogen molecule H2
H
Atomic no.
- Electronic
configuration
H
xH
x
x
x
H: H
1
1
1
H
Bonding
H
1
1
H
H
Amani Hamdi
Page 31
4. A Hydrogen chloride molecule HCl
H
Atomic no.
- Electronic
configuration
5. A chlorine molecule Cl2
Cl
Atomic no.
- Electronic
configuration
6. A methanol molecule
CH3OH
Atomic no.
- Electronic
configuration
1
1
17
2,8,7
C
4H
Bonding
17
2,8,7
Cl
17
2,8,7
17
2,8,7
Cl
1
1
O
8
2,6
Amani Hamdi
Page 32
7. An ethanol molecule C2 H5 OH
2C
Atomic no.
- Electronic
configuration
17
2,8,7
6H
1
1
O
8
2,6
Example of double covalent bond in molecules:
8. An Oxygen molecule O2
O
Atomic no. 8
- Electronic 2,6
Configuration
O
O
8
2,6
O
O
9. An ethene molecule C2 H4
O
2C
Atomic no.
- Electronic
configuration
17
2,8,7
Bonding
4H
1
1
Amani Hamdi
Page 33
Example of triple covalent bond in molecules:
N
A nitrogen molecule N2
Atomic no. 7
Electronic 2,5
configuration
N
7
2,5
N
Comparison between ionic and covalent compounds:
Properties of typical ionic Compounds Properties of simple covalent Compounds
They are crystalline solids at room
temperature.
They are often liquid or gases at
room temperature.
They have high melting and boiling points. They have low melting and boiling points.
Volatile
Non-Volatile
They are often soluble in water (not
usually soluble in organic solvents, e.g.
ethanol, methylbenzene).
They are soluble in organic solvents such
as ethanol or methylbenzene (very few are
soluble in water).
They conduct electricity when molten or
dissolved in water (not when solid).
They do not conduct electricity.
Bonding
Amani Hamdi
Page 34
Material structure
There are four types of solid physical structure
Metallic Structure (Metal crystals)
 Metal atoms have relatively few
electrons in their outer most shells.
When they are packed together
each metal atom loses its outer
electrons into “sea” of free
electrons (or mobile electrons).
 The atoms are no longer
electrically neutral; they became
ions because they have lost electrons.
 Therefore the structure of a metal is described as positive ions
packed in a lattice surrounded by a sea of mobile electrons
(delocalized electrons).
Material Structure
Amani Hamdi
Page 35
Delocalized electrons: Electrons those are not restricted to orbiting
one positive ion.
Lattice: Three dimensional regular arrangements of atoms, molecules or
ions in a crystalline solid.
Metallic Bonding: The electrostatic attraction force between the sea of
mobile electrons and the regular array of positive metal ions within a
solid metal.
Properties of metals due to their structure:
1. High density: metals are high in density due to their close packing of
ions.
In some metals the ions are less closely packed. These metals have the
lowest densities of all metals for example the alkali metals.
2. Metals are good conductors of heat due to the movement of the
mobile free electrons.
3. Metals are good electric conductor due to the presence of free
electrons.
4. Metals are malleable because the layers of identical ions can slide
over one another without breaking the structure, due to strong metallic
bonding.
5. Metals are ductile (can be stretched into wires) due to the strength of
the metallic bonds that is strong but not rigid (metals have a high
tensile strength).
Material Structure
Amani Hamdi
Page 36
Giant Ionic Lattice (Ionic crystals)
 Ionic compounds structure:
lattices of positive and negative ions.
 The nearest neighbors of the ion are
always of the opposite charge.
Example: in Sodium Chloride
 Each Sodium ion Na+ is surrounded by six Chloride ions Cl- and each
Chloride ion is surrounded by six Sodium ions Na+.
 The actual arrangement of the ions in the other compounds depends
on the number of ions involved and on their sizes.
Properties of the Ionic crystals:
 Ionic crystals are hard but much brittle than metallic crystals. Ionic
crystals are hard because pushing one layer against another in an ionic
crystal bring ions of the same charge next to each other. The repulsion
forces the layers apart.
 Ionic lattices dissolve in water. When an ionic crystal dissolves, each ion
becomes surrounded by water molecules. This breaks up the lattice and
keeps the ions apart. For those ionic compounds that do not dissolve in
water, the forces between the ions must be very strong.
 Ionic compounds can conduct electricity when dissolved in water or
when they are melted because, the ions are able to move and carry
the current.
Material Structure
Amani Hamdi
Page 37
Simple Molecular Structure (Molecular Crystals)
Structure : Lattices of molecules .
Some non-metals (e.g. Iodine and Sulfur) and some covalent bonded
compounds exist as solids with low melting points. In these crystals
molecules of these elements or compounds are held together by weak
intermolecular forces to form crystals that are easily broken down by
heat.
Properties of Simple molecular structure:
 Molecular structure does not conduct electricity because they have no
charges.
 Molecular structures have low melting and boiling points. This is
because there are only weak forces between the molecules (Van der
Waals forces).
Material Structure
Amani Hamdi
Page 38
Giant Molecular Crystals (Macro Molecules)
This type of structure occurs either between atoms of an element such as
Carbon atoms in Graphite and Diamond or in compounds such as Silica
SiO2 (sand) and Germanium Oxide GeO2.
Graphite structure:
Van dear
weal’s
weal’s
forces
How the layers fit together
One layer of
graphite
 It is a giant molecular structure composed of carbon atoms. Carbon
atoms are arranged in flat layers. Each carbon atom is bonded to other
three carbon atoms by strong covalent bonds. Between these layers,
there are weak forces of attraction (Van der Waals forces).
 Graphite is soft and feels slippery because it is layered structure with
weak forces of attraction between the layers, so layers are able to slide
over each other.
 Graphite conducts electricity due to free electrons.
Note: In graphite each carbon atom uses only three electrons of the four
valency electrons that are used by the layered atoms in covalent bonding.
There is still an electron from each atom to move between layers, this is
why graphite conducts electricity.
Material Structure
Amani Hamdi
Page 39
Diamond Structure:
C
C
C
C
C
Diamond is a form of carbon. Each carbon atom is attached to other
four carbon atoms by covalent bonds in a tetrahedral structure.
Properties of diamond:
 Diamond has high melting point.
 Hard because the strong covalent bonds extends throughout the
whole structure.
 Brittle due to rigidity of bonds.
 Diamond does not conduct electricity because there are no free
electrons.
Note: diamond has no free electrons as all the four valency electrons are
used in bonding.
Material Structure
Amani Hamdi
Page 40
A comparison of the properties and uses of diamond and graphite:
Diamond
Appearance
Hardness
Density
Graphite
Properties
Uses
Properties
Colorless,
transparent crystals
that sparkle in light
In jewelery and
ornamental
objects
Dark grey, shiny solid
The hardest natural
substance
In drill bits,
diamond saws
and glass-cutters
Soft-the layers can
slide over each
other-and solid has a
slippery feel
More dense than
graphite(3.51g/
Electrical
Conductivity
Uses
In pencils, and as
a lubricant
Less dense than
diamond(2.25g/
Does not conduct
electricity
Conducts electricity
As electrodes
and for the
brushes in
electric motors
Silicon (IV) Oxide (silica)
O
Silicon (IV) Oxide has a giant molecular
structure. Sand and quartz are examples of
silica. (Silicon (IV) oxide or silicon dioxide
SiO2)
Si
O
O
O
Si
O
O
O
Structure of silica:
Each Silicon atom is attached to four oxygen
atoms by covalent bonds in a tetrahedral
structure and each oxygen atom is attached to two silicon atoms.
Material Structure
Amani Hamdi
Page 41
Properties of silicon dioxide:
 Hard.
 High melting and boiling point.
 Does not conduct electricity.
Note: Diamond and Silicon dioxide have similar tetrahedral structure and
so similar properties.
Material Structure
Amani Hamdi
Page 42
Elements
An element is a substance which cannot be further divided into simpler
substances by chemical methods. It is formed of only one type of atoms.
• There are 94 naturally occurring elements. Most of elements (70) can be
classified as metals.
• Metals are separated from non-metals in the periodic table.
The non-metals are grouped into the top right region of the periodic
table above the thick stepped line.
• The chemical properties of metals and non-metals are different.
Comparison between metals and non-metals:
Metals
Non-Metals
1. They are usually solids, (except for mercury,
which is liquid) at room temp
1.They are solids or gases (except for bromine
which is liquid) at room temp.
2. Have high melting point and high boiling point.
2.Have low melting and a boiling point.
3. All metals Conduct electricity.
3.Don’t Conduct electricity (except graphite, a
form of carbon) They tend to be insulators.
4. They are good conductor of heat
4.They are poor thermal conductor.
5. They are malleable (their shape can be
changed by hammering. They are ductile (can
be pulled out into wires)
5.Most non-metals are brittle when solid.
6. They are grey in colour(except for gold and
copper)
6.They vary in colour they have a dull surface
when solid
7. They make a ringing sound when struck (They
are sonorous)
They are not sonorous
Elements
Amani Hamdi
Page 43
Family profile of some groups
Group I The alkali metals
-Metals of group I are called alkali metals. They are the most
reactive metals. They are known as alkali metals because they
react vigorously with water producing Hydrogen and alkaline
solution.
-Alkali metals are Lithium, Sodium, Potassium, Rubidium, Cesium
and the radioactive element Francium.
Physical Properties of alkali metals
• They are soft solids.
• They have relatively low melting points.
• They have low densities.
Chemical Properties of alkali metals
• They are highly reactive, so they are stored in oil to prevent
them reacting with oxygen and water vapour in the air.
• They have a valency of +1
Note:
• When freshly cut with knife all these metals have a light grey,
silvery surface which quickly tarnishes (becomes dull)
Alkali metal trends
• Reactivity increases as we go down the group. All group I reacts
with water. The reaction ranges from vigorous in case of Lithium to
explosive in case of Cesium.
• Melting and boiling points decrease down the group.
• Density increases down the group. Lithium, Sodium and
Potassium are less dense than water (density of water is 1 gcm-3)
so they float over water.
Elements
Amani Hamdi
Page 44
Group II(the alkaline earth metals)
-Group II is called the alkaline earth metals. The elements of this
group are: Beryllium, Magnesium, Calcium, Strontium, Barium,
and the radioactive element Radium. Group II shows similar
trends in reactivity to group 1, but are less reactive.
-The reactivity increases going down the group. Beryllium (at the
top) is the least reactive and Barium at the bottom is the most
reactive.
Group VII( Halogens)
The most reactive non-metals are halogens in group VII of the
periodic table
They are all diatomic non-metals (for example, F2,Cl2,Br2,I2)..
Physical properties of halogens
• They have a similar strong smell.
• Poor electric conductors.
• Low melting and boiling points .
Chemical properties of halogens
• They have a valency of -1.
• They react directly with metals to form halide salts.
• They are all poisonous
Trend of group VII
•
•
•
•
The reactivity decreases down the group.
The melting and boiling points increase down the group.
Density increases down the group.
The elements change from gases to liquid to solids as we go down the
group.
• The colours of the elements get darker as we go down the group.
Elements
Amani Hamdi
Page 45
Halogen
State
Colour
F2
Gas
Pale yellow
Cl2
Gas
Yellow-green
Br2
Liquid
Red-brown
I2
Solid
Dark grey
At2
Solid
Black
Transition elements
-They are elements that lie between group II and group III
beginning from the 4th period.
-This block of elements includes many elements you are familiar
with for example, Copper, Iron and Zinc.
Physical properties of Transition elements
-They are harder and stronger than metals of group I and II.
-They have much higher densities than metals of group I and II.
-They have high melting points (except for mercury which is liquid
at room temperature).
- A few of the metals are strongly magnetic (Iron,Cobalt & Nickel).
Elements
Amani Hamdi
Page 46
Chemical properties of Transition elements.
• Many of their compounds are coloured.
• They have more than one valency (oxidation state);
they form more than one type of ions for example, Iron
can form Fe+2 and Fe+3 ions.
• The transition elements and their compounds often make
useful catalysts.
• They are less reactive than the other metals
Noble gases (group Zero)
-The elements of this group are Helium, Neon, Argon, Krypton,
Xenon and the radioactive element Radon.
-They are non-metals.
-They exist as monoatomic molecules (individual atoms).
Physical properties of Noble gases
-They are colorless gases
-Their melting points and boiling points are extremely low.
Chemical properties of Noble gases
-They are very unreactive as they have completely filled
outermost shell.
Elements
Amani Hamdi
Page 47
 The uses of Nobel gases depend on this inertness.
• Helium is used in airships and balloons because it is both
light and unreactive.
• Argon is used to fill light bulb because it does not react with
the filament even at high temperature.
• Neon is used in advertising and lasers.
Uses of some metals
Uses
Properties
1. Aluminum is used in cooking
utensils
Resists corrosion
Good conductor of heat.
It has a high tensile strength and
light (low density)
2. Aluminum is used in the
construction of aircraft.
5. Aluminum is used in making
overhead power lines.
Resists corrosion
(as it is covered with non - porous
protective oxide layer )
Good electric conductor and has
low density.
With a steel core
To strengthen the cable
6. Cupper is used in making electric
power cables.
7. Cupper is used in making cooking
pans.
Good electric conductor and
ductile.
3. Aluminum is used in kitchen foil
4. Aluminum is used in Can
8. cupper is used in making of water
pipes.
9. Iron is used in construction of
bridges
10. Tin is used in coating tin cans
Good heat conductor , has high
melting point and resists
corrosion.
Cupper does not react with water
and resists corrosion
Hard.
Not poisonous
Elements
Amani Hamdi
Page 48
Recycling metals:
Recycling a metal involves collecting used metal items and
producing new metal from them . The steps usually needed are :
 Collecting and transporting the used items to a recycling centre
 Breaking up and sorting the different metals
 Removing impurities from the metals
The metals can then be used to manufacture new metal items.
Advantages of recycling metals:
the advantage of recycling compared to producing metals from
metal ore include :
 more economic - less energy is needed to produce a metal
 less damage to the environment - fewer quarries and mines
 less noise and less heavy traffic .
 saves valuable raw materials as reserves of metal ores will last
longer
Elements
Amani Hamdi
Page 49
Reactions of Metals with Air, Water and Dilute Acids
We can get information on reactivity by investigating the following
aspects of metal chemistry:
• Ease of extraction.
• Reactions with air and water.
• Reactions with dilute acids.
• Metal displacement reactions and Redox reactions.
•
Heat stability of metal compounds.
The overall picture is
summarized in what is known
by the reactivity series of
metals.
The reactivity series of metals is
an order of reactivity giving the
most reactive metal first.
Elements
Amani Hamdi
Page 50
Reaction of Metals with Air
K
Na
Burn in air producing oxides.
Ca
Mg
Al is a reactive metal that is covered with non-porous protective
oxide layer. Al will burn only when the layer is removed.
Zn
Fe
Sn
Do not burn but hot metal glows and covers by oxide film
Pb
Cu
Ag
Au
Do not react
Pt
Elements
Amani Hamdi
Page 51
Chemical equations to show the previous reactions
Metal + Oxygen
Metal Oxide
Sodium + Oxygen
Na + O2
Sodium Oxide (word equation)
Na2O (symbolic equation)
The previous equation is not balanced as the number of atoms of
any element must be equal at both sides as matter is
neither created nor destroyed.
So you have to insert numbers in front of the chemicals to
balance the equation:
4Na + O2
2Na2O
Magnesium + Oxygen
2Mg + O2
Magnesium Oxide
2MgO
Elements
Amani Hamdi
Page 52
Reactions of Metals and Water
K
Na
Very reactive metals react with cold water
producing Metal Hydroxide and Hydrogen.
Ca
2K + 2H2O
2KOH + H2
2Na + 2H2O
2NaOH + H2
Ca + 2H2O
Ca(OH)2+ H2
Mg
Al
React with steam producing Metal Oxide and Hydrogen.
Al will react only when its non-porous oxide is removed.
Zn
Fe
Mg + H2O
MgO + H2
Sn
Zn + H2O
ZnO + H2
Pb
Cu
Ag
Don’t react with water.
Au
Pt
Elements
Amani Hamdi
Page 53
Note: Magnesium reacts very slowly with cold water, but reacts
vigorously when heated with steam.
Remember that as we go down, the group of alkali metals, the
reactivity increases.
Li
Lithium reacts steadily with water; the metal
does not melt and hydrogen does not ignite.
Na
Sodium reacts more strongly; the metal melts and Hydrogen
Ignites.
K
Potassium reacts vigorously with water and Hydrogen ignites
spontaneously. Potassium may explode dangerously.
Increase
s
If you place a small piece of Sodium in water :
1. it floats and reacts very quickly.
2. The reaction is exothermic and the heat produced melts the
Sodium.
3. The molten Sodium dart around the water surface
4. A yellow flame is seen.
5. You may see effervescence (fizz) as Hydrogen evolves.
Elements
Amani Hamdi
Page 54
Displacement reactions of metals
According to the reactivity series:
 More reactive metals can displace less reactive metals in their
salt solutions.
Mg(s) + CuSO4(aq)
MgSO4(aq) + Cu(s)
 Magnesium is more reactive than Copper.
 Metals above Hydrogen in the chemical reactivity series react
with dilute acids producing salt and Hydrogen.
Zn(s) + 2HCl(aq)
ZnCl2(aq)+ H2(g)
 Zinc is more reactive than Hydrogen
Cu(s) + HCl(aq)
No reaction
 Copper is less reactive than Hydrogen.
Elements
Amani Hamdi
Page 55
Alloys
An Alloy is a mixture of elements usually metals. Alloys are
formed by mixing the molten metals together thoroughly and
then allowing them to cool and form a solid.
• Alloys are designed to have the
properties useful for a particular
purpose.
• An alloy is stronger than the
original individual metals.
• Look at the fig. you will see that in
case of pure metals, layers can
slip easily over each other as
all the layers are made of same
sized atoms. In case of Alloys,
the impurities (the different
type of atoms) reduce the
slippage because the atoms
are of different size making the
alloy harder than pure metals.
Elements
Amani Hamdi
Page 56
The following table shows some important alloys, their composition, their
properties and uses.
Alloy
Composition
Copper
70%
Brass
Zinc
30%
Copper
90%
Bronze
Tin
Stainless steel
Mild steel
10%
Iron
74%
Chromium 18%
Nickel
8%
Iron
Carbon
Properties
• Harder than pure
copper
• Gold coloured
• Harder
than pur e
copper
• Harder than pure iron
• Does not rust
99.7% • Stronger and
0.3%
harder than pure
iron
Elements
Uses
• ornaments
• ornaments
• Cutlery
• Surgery tools
• Chemical plants
• Car bodies
• machinery
Amani Hamdi
Page 57
Rusting of iron and its prevention
 When a metal is attacked by air,
water or other surrounding
substances, it is said to corrode.
In the case of iron and steel, the
corrosion process is known as
rusting.
 Rust is a red- brown powder
consisting mainly of hydrated
iron oxide (Fe2O3.2H2O).
 Water and oxygen are essential
for iron to rust.
 Sea water increases the rate which iron objects rust.
Rust prevention
Iron can be prevented from rusting by means of many ways.
1 . By Barrier Methods : Isolating iron from oxygen and water
a. Painting:
Ships, Lorries, cars, bridges and many other iron and steel
structures are painted to prevent rusting however, if the paint
is scratched, the iron beneath it will start to rust.
b. Oiling and greasing:
The iron and steel in the moving parts of machinery are coated
with grease to prevent them from rusting, but the protective
film of grease must be renewed.
Elements
Amani Hamdi
Page 58
c. Plastic coatings:
These are used to form a protective layer on items such as
refrigerators.
d. Electroplating:
An iron or steel can be electroplated with a layer of Chromium
or Tin. A Tin can is made of steel coated in both sides with tin
because tin is unreactive and non-toxic. If the protective layer
is broken, then the steel beneath will begin to rust.
e. By Galvanisation:
 Galvanisation is a process where iron is protected , when
coated with a layer of zinc .
 This can be done by electroplating or dipping iron into zinc
 The zinc coat react with Oxygen producing Zinc oxide that
react with the moisture producing Zinc Oxide that reacts with
the moisture producing Zn(OH)2 , that react with CO2
producing ZnCO3 that protects iron by the barrier method .
 If the coating is damaged the is still protected by sacrificial
protection.
Elements
Amani Hamdi
Page 59
2. By Sacrificial protection:
 This is a method of rust prevention in which blocks of a
reactive metal are attached to the iron surface.
 Zinc or Magnesium blocks are attached to oil rigs and to the
halls of ships.
 The more reactive metal,Zinc or Magnesium will corrode in
preference to iron.
 In sacrificial protection, the more reactive metal, Zinc or
Magnesium loses electrons and oxides in preference to iron
and these electrons flow to iron preventing iron from rusting
forming. (Iron(III)Oxide).


Elements
Amani Hamdi
Page 60
3. By Electrolytic protection (cathodic protection)
Huge structures like oil-rig can be protected by using Iron as
cathode (connected to the negative pole of the battery). Inert
electrode is used as the anode (e.g. Titanium) and a power supply
is required.
The figure shows electrolytic protection of oil rig.
Elements
Amani Hamdi
Page 61
Colours
Elements
Metals
Compound
Non-metals
covalent
Except:
NO2
Except:
Gold: Yellow
F Yellow
O2 ,H2 , N2
All are colourless
Ionic
C Black
SYellow
BWhite
Br Red-brown
Dark grey
At Black
Ionic compounds of
group 1,2 ,3 are white
Ionic compounds of
coloured
solution
Note: Iodine is dark gray solid at room temperature .when sublimes, it gives purple fumes .In solutions it is Yellow-brown
-Solutions of halides (ions of halogens) are colourless
Colours
Amani Hamdi
Page 62
Colours of some transtion compounds
 Most Copper II compounds are blue
Cu(OH)2
CuSO4.5H2O
Cu(NO3)2
CuCl2
CuCO3
CuO
Blue
Blue - Green
Green
Black
 Most Iron II Compounds are green
Fe(OH)2
FeO
 Most Iron III Compounds are red-brown
Fe(OH)3
Fe2O3
 Colours of some oxidizing agents
-Potassium Chromate (VI) (K2Cr2O7) Orange
Reduction
-Potassium Manganate (VII) (KMnO4)Violet
Reduction
Green
Colourless
 Colours of some hydrated salts
Hydrated CoCl2.6H2O (Pink)
Hydrated CuSO4.5H2O(Blue)
Dehydration
Dehydration
Anhydrous CoCl2 (Blue)
Used to test
for water
Anhydrous CuSO4 (White)
Amani Hamdi
Colours
Page 63
Chemical reactions
A chemical reaction is a change in which a new substance is
formed.
Generally the process is not easily reversed. During a chemical
reaction, energy can be given out (exothermic reaction) or taken
in(endothermic reaction).
A physical change is the change in which the substances do not
change identity. They can be easily returned to their original form
by some physical processes. Examples of physical changes are:
 Change in state of matter. Melting, freezing, evaporation
and condensation are physical change.
 Dissolving a substance in water.
 Grinding the substance such as salts or sugar.
A chemical equation links together the names of substances that
react (the reactants) with those of the new substances formed
(products).
Examples
heat
Magnesium + Oxygen  Magnesium Oxide (Word equation)
Reactants
Products
2 Mg + O2  2 MgO (symbolic equation)
This is a balanced equation, the number of each type of atoms are
the same on both the reactant side and product side, two
Magnesium atoms and two Oxygen atoms at each side.
Amani Hamdi
Chemical Reactions
Page 64
Chemical
Reactions
Synthesis
Combustion
Displacement
Single
Displacement
Decomposition
Double
Displacement
Acid-Base
Neutralization
Ionic
Precipitation
Synthesis reactions
This type occurs where two or more substances react together to
from one product.
Examples:
Iron + Sulfur
Iron(II)Sulfide
Fe
FeS
+
S
Magnesium + Oxygen  Magnesium Oxide
2Mg
+ O2
Hydrogen + Oxygen
2H2
+ O2
 2 MgO
 water
 2 H2O
Amani Hamdi
Chemical Reactions
Page 65
Note: Photosynthesis is a very essential process for life.
Photosynthesis is a process by which plants make their food
(glucose) by absorbing carbon dioxide from air, water from soil
and sunlight trapped by chlorophyll.
Chlorophyll acts as catalyst.
It is a synthesis reaction. , It is an endothermic reaction.
Carbon dioxide + water
6 CO2
sunlight

Glucose + Oxygen
sunlight
+ 6 H2O  C 6 H12 O6 + 6O2
Displacement Reactions
Double Displacement
Reaction
Simple Displacement
Reaction
Neutralization
Reaction
Precipetation
Reaction
Double displacement reaction:
In double displacement reaction, two ionic compounds exchange their
ions.
A+B- (aq)+ C+D(aq
)
AD + CB
Amani Hamdi
Chemical Reactions
Page 66
A) Neutralization reaction:
Neutralization is a chemical reaction between an acid and a base
(or alkali) to produce salt and water only.
Examples:
HCl + NaOH
Acid + alkali
NaCl + H2O
salt + water
H2SO4+ CuO
Acid + base
CuSO4 + H2O
salt + water
Note: Metal Oxides and Metal Hydroxides are bases.
Bases that dissolve in water become alkali.
B) Precipitation Reaction:
Precipitation reaction involves the formation of an insoluble
product.
Precipitation is the sudden formation of an insoluble salt when
two solutions are mixed or when a gas is bubbled into a solution.
-This type of reaction is used to prepare insoluble salts.
Examples:
Pb(NO3)2 (aq) + 2KI(aq)
PbI2(s)
+ 2KNO3(aq)
Insoluble salt Yellow ppt.
-The downward arrow shows that PbI2is insoluble forming a
precipitate.
-The insoluble salt (PbI2) can be separated from the soluble salt
(KNO3) by filtration.
Amani Hamdi
Chemical Reactions
Page 67
-The lime water test for Carbon dioxide also depends on
precipitation. When Carbon dioxide is passed through lime water
Ca (OH)2 solution, an insoluble product CaCO3 is formed that
causes turbidity.
CO2(g)+ Ca(OH)2(aq)
CaCO3(s) + H2O(l)
Simple displacement reaction
 More reactive metal can displace a less reactive metal from its
salts.
Mg + CuSO4
MgSO4 + Cu
(Magnesium is more reactive than cupper)
 Metals above hydrogen in the reactivity series are more reactive
than hydrogen, so they can react with acids as the metal displaces
hydrogen.
Mg + 2HCl
MgCl2 + H2
 Halogens (elements of group VII) displace halides of less reactive
halogens from their salts.
F  the most reactive halogen
Cl
Br
I
At  least reactive halogen
Amani Hamdi
Chemical Reactions
Page 68
Cl2
+
2KI

Green gas
Colourless soln.
Cl2
+
Green gas
2KBr
2 KCl
+
Brown liquid
I2
colourless soln.

Colourless soln.
Br2
+
2 KCl +
colourless soln.

2KI
Colourless soln.
Yellowish brown
Br2
Brown liquid
2 KBr
+
colourless soln.
I2
Yellowish brown
Oxidation-Reduction Reactions (Redox Reactions)
And Combustion
Chemists’ ideas about oxidation and reduction have been
expanded to a wide range.
Oxidation is a chemical process in which a substance gains oxygen
during a reaction.
Reduction is a chemical process in which a substance loses oxygen
during a chemical reaction.
Example:
heat
Cupper (II) Oxide + Hydrogen    Cupper + water
reduction
heat
CuO + H 2   Cu + H2O
Oxidation
CuO is an oxidizing agent.
H2 is reducing agent.
 Colour changes from black to reddish brown.
Amani Hamdi
Chemical Reactions
Page 69
reduction
2Fe2O3+ 3C  4 Fe + 3 CO2
Fe2O3 is an oxidizing agent.
Oxidation
C
is a reducing agent.
The most common oxidizing agents are:
Oxygen (or air), Hydrogen peroxide, Acidified Potassium
Manganate (VII) and Acidified Potassium (VI)chromate.
The most common reducing agents are:
Hydrogen, Carbon, Carbon monoxide, and Sulfur dioxide
- Aqueous potassium iodide KI (aq)
Colorless solution of KI turns brown due to the formation of iodine
2I- (aq)
I2 + 2eOxidation is the loss of electrons
A new definition
Remember this by :
OIL
Oxidation
Is
Losing e’
RIG
Reduction
Is
gaining e’

Examples :
Sodium + Chlorine
2Na
Nao
Clo
+ Cl2
Loses 1eGains 1e+
Na+
Cl-

Sodium Chloride

2 Na+Cl(oxidation)
(Reduction)
During this reaction, the oxidation state of Sodium has increased by 1 from 0
to +1 and the oxidation state of Chlorine has decreased from 0 to –1
Amani Hamdi
Chemical Reactions
Page 70
 Thus another definition for oxidation and reduction has
to be included:
Oxidation is the increase in oxidation state of an atom or an ion.
Reduction is the decrease in oxidation state of an atom or an ion.
e.g.
reduction
Zn0(s)+ Cu+2SO2-4(aq)  Zn2+ SO2-4(aq)+ Cu0
oxidation
Zn is oxidized.
Cu2+ is reduced.
The oxidation state of Zinc has increased by 2, from 0 to + 2.
Meanwhile the oxidation state of Copper has decreased by 2,
from + 2 to 0
e.g.
Re
reduction
Cl02(g) + 2K1+I1-(aq)
2K1+Cl1-(aq) +I02(aq)
oxidation
-The oxidation state of iodide changes form –1 to 0. It has
increased. Iodide has oxidized.
-The oxidation state of Cl changes from 0 to –1. It has decreased.
Chlorine is reduced to chloride ions.
An oxidizing agent (Oxidant): a substance which will oxidize
another in a redox reaction.
An Reducing agent (Reductant ):a substance which will reduce
another in a redox reaction.
Amani Hamdi
Chemical Reactions
Page 71
Rules of Oxidation States
Rule
Example
1. The Oxidation number of any
uncombined element is Zero
H2
Zn
O2
2. Many elements or ions have fixed
oxidation number in compounds
Group 1 elements are always +1
Group 2 elements are always +2
Fluorine is always -1
Hydrogen is +1 (except for in metal
hydrides like NaH , where it is -1 )
Oxygen is -2 (except in peroxides , where
it is -1 and F2O where it is +2 )
3. The oxidation number of an
element in monoatomic ion is
always same as the charge
Zn 2+ Oxidation number = +2
Fe 3+ oxidation = +3
Cl- oxidation number = -1
4. The sum of the oxidation number in
a compound is zero
NaCl


Oxidation number Na = +1
Oxidation number Cl = -1
Sum oxidation number = 0
5. The sum of oxidation number in ion
is equal to the charge on the ion
SO4 2- Oxidation number of S = +6
Oxidation number 4 O atoms = 4x (-2)
Sum oxidation number = -2
Amani Hamdi
Chemical Reactions
Page 72
Combustion
Combustion: the reaction of a substance with Oxygen causing the
release of energy.
The reaction is exothermic and often involves a flame.
Burning: combustion in which a flame is produced.
-The combustion of natural gas is an important source of energy
for homes and industry. Natural gas is mainly Methane. Its
complete combustion produces Carbon dioxide and water vapour.
Methane + Oxygen
CH4 + 2 O2
carbon dioxide + water
CO2 +
2H2O
-Substances that undergo combustion readily and give out a large
amount of energy are known as fuel.
-Our bodies get their energy from food, in a process called
respiration.
Respiration: is the breaking down of food in body cells to release
energy.
Amani Hamdi
Chemical Reactions
Page 73
Energy and chemistry
(Heat changes in chemical reactions)
Energy cannot be created nor destroyed (law of conversation of
energy). However energy can be changed from one form to
another.
Heat of reaction (heat change):
 It is the amount of energy taken in or given out, it is measured
by kilojoule per mole (KJ/mol).
1 kilojoule = 1000 joule
 Heat energy is given the symbol ΔH (pronounced delta aitch)
 Energy changes occur in some chemical reactions or even in
some physical processes such as when a solid dissolves in water.
 Chemical reactions in which heat is given out are described as
exothermic and those in which heat is taken in are
endothermic.
Note:
 In an exothermic reaction, the temperature of the reaction
mixture initially rises until the highest temperature is reached.
When the reaction is completed, the temperature falls until it
reaches the room temperature.
 In an endothermic reaction, the temperature of the reaction
mixture falls until the lowest temperature is reached. When
the reaction is completed the temperature of the reaction
mixture rises until it reaches the room temperature.
Energy And Chemistry
Amani Hamdi
Page 74
Exothermic reactions
Definition
Characteristics
of the
reaction
Examples
Endothermic reactions
Reactions that give out heat
energy to the surrounding.
-Heat is liberated and is
transferred from the chemicals
to the surrounds.
Reactions that absorb heat
energy from the surrounding.
-Heat is absorbed and is
transferred from the
surrounds to the reactants.
-The temperature of the
reaction mixture rises, the
container feels hot.
-The temperature of the
reaction mixture falls, the
container feels cold.
-Heat of the reactants is more
than heat of products.
 Combustion of fuel.
 Simple displacement
reaction.
 Neutralization reaction.
 Reactions in cells.
 Respiration.
 Condensation.
 Freezing.
 Iron rusting.
-Heat of the reactants is less
than heat of products.
 Thermal decomposition.
 Electrolysis.
 The action of light on
silver bromide in
photographic film.
 Photosynthesis.
 Melting.
 Evaporation.
 If the reaction is exothermic, i.e. heat is given out; ΔH has a
negative value (as the reactants lose energy).
 If the reaction is endothermic, i.e. heat is taken in; ΔH has a
positive value (as the reactants gain energy).
Energy And Chemistry
Amani Hamdi
Page 75
During a reaction, all bonds of the reactants are broken, this takes
energy in, so
 Breaking chemical bonds takes energy from the surrounding.
This is an endothermic process.
New bonds are then formed to give products. Formation of bonds
releases energy.
 Formation of bonds gives out energy to the surrounding. This is
an exothermic process.
Examples
 Burning methane in oxygen.
CH4(g)
+
2O2(g)
CO2(g) +
2H2O(g)
+
+
Bonds that are broken
4 C H bonds
2O
O bonds
Energy And Chemistry
Bonds that are formed
2C
O
4O
H
Amani Hamdi
Page 76
If the energy absorbed in bond breaking is more than the energy
Released in bond formation, so the reaction is endothermic.
If the energy released in bond formation is more than the energy
absorbed in bond breaking, so the reaction is exothermic.
Bond energy: it is the energy required to break one mole of
bonds.
The overall change in energy for a reaction can be shown in an
energy level diagram (or energy profile)
Energy profile for an exothermic reaction:
Burning Methane in Oxygen is an exothermic reaction.
CH4(g) + 2O2(g)
CO2(g) + 2H2O(g)
ΔH = negative value.
Energy And Chemistry
Amani Hamdi
Page 77
Energy Profile for an endothermic reaction:
 The reaction between Nitrogen and Oxygen is an
endothermic reaction.
N2(g) + O2(g)
2NO(g)
ΔH = positive value
Energy And Chemistry
Amani Hamdi
Page 78
Energy Profile for an endothermic and exothermic reactions with
activation energy Ea :


Energy Profile for an endothermic and exothermic reactions with Catalyst:
 Ea : Activation energy without using a catalyst .
 E'a : Activation energy with using a catalyst .
Energy And Chemistry
Page 79
Amani Hamdi
Worked example :
 Reaction between Hydrogen and Chlorine to produce
Hydrogen Chloride.
H2(g) + Cl2(g)
2HCl(g)
If the bond energies of:
Cl – Cl
H–H
H – Cl
242 KJ.
436 KJ.
431 KJ.
Calculate the heat change and deduce if the reaction exothermic
or endothermic.


Solution:
Energy taken in to break bonds
For a mole of H2 molecule
436 KJ
For a mole of Cl2 molecule
242 KJ
Total energy in
678 KJ
Energy given out from bond formation:
For 2 moles of HCl
2 × 431 = 862
Energy in – energy out
= + 678 KJ - 862 KJ = -184 KJ
+ve sign as energy is gained
-ve sign as energy is lost
Generally:
-ve sign indicates that the
reaction is exothermic
ΔH = + Energy in – Energy out
 So the reaction gives 184 KJ more energy than it takes in. Since
it gives out energy, the reaction is exothermic.
Energy And Chemistry
Amani Hamdi
Page 80
Acids and Bases
An Acid: is a substance that dissolves in water producing
hydrogen ions.
 Hydrogen ion is also known as a proton, so an acid can be defined
as a proton donor.
 Acids present in animals and plant material are known as organic
acids, e.g. ethanoic acid in vinegar and methanoic acid in antsand
nettle stings.
 Acids in food make it sour, e.g. vinegar, lemon and grapefruit.
 Other acids are corrosive .They are dangerous on skin and some
are able to attack metalwork and stonework. These powerful acids
are called mineral acids, e.g. Hydrochloric acid and Sulfuric acid.
 Acids also can be classified into strong and weak acids.
Strong acid: an acid that is completely ionized when dissolved in
water producing high concentration of H+(aq) in solution.
e.g. Hydrochloric acid.
Weak acid: an acid that is partially dissociated in water
producing low concentration of H+(aq) in solution.
e.g. Ethanoic acid.
 Number of hydrogen ions that can be donated by one molecule
of acid is called basicity.
Acid and Alkalis
Amani Hamdi
Page 81
Common acids
Acid
Formula
Ions present
Basicity
Hydrochloric acid HCl
H+ , Cl( chloride)
Monobasic
Nitric acid
HNO3
H+, NO-3
(nitrate)
Monobasic
H2SO4
2H+, SO4-2
(sulfate)
Dibasic
3H+, PO4-3
(phosphate)
Tribasic
Sulfuric acid
Phosphoric acid H3PO4
Ethanoic acid
CH3COOH
H+ ,
Acid and Alkalis
CH3COO(ethanoate)
Monobasic
Amani Hamdi
Page 82
Reactions of Acids
Reaction
Metal + acid
Salt + hydrogen
Equation
Magnesium+ Hydrochloric acid
Magnesium chloride + Hydrogen
Mg(s) + 2HCl(aq)
MgCl2(aq) +
Base + acid
Sodium hydroxide + Hydrochloric acid
Salt + water
NaOH(aq) + HCl(aq)
(neutralization reaction)
Carbonate salt + acid
Calcium carbonate + Sulfuric acid
salt + water +
carbon
dioxide
CaCO3(s) + H2SO4(aq)
H2(g)
Observation
Bubbles of
Colourless gas.
Lighted
splint
burns with pop
sound.
Sodium Chloride + water
NaCl(aq)
+ H2O(l)
Calcium sulfate + water + Carbon dioxide
CaSO4(s)
+ H2O(l) + CO2(g)
Effervescence
of a gas that
Turns lime
water milky.
Note: if you are asked to suggest a metal with an acid, do not go with very reactive metals such as
Ca.
Acid and Alkalis
Amani Hamdi
Page 83
Bases
 Most metal oxides and metal hydroxides are bases.
 A base is a substance that neutralizes an acid to form a salt and
water only.
 A base is a proton acceptor. (Remember that an acid is a proton
donor. A proton is H+)
NH3 + H2O
NH4+ + OHBase (proton acceptor)
Acid (proton donor)
In this equation you will find that H+ is transferred from H2O to
NH3, So NH3 here acts as a base because it is a proton acceptor
and water acts as an acid because it is a proton donor.
HCl + H2O
H3O+ + ClAcid (proton donor)
Base (proton acceptor)
 Most bases are insoluble in water; those that dissolve in water are
called alkalis.
 The common alkalis are NaOH, KOH, Ca(OH)2 and NH4OH
 An alkali is a soluble base which produces OH-(aq) ion in water.
 Alkalis feel soapy to skin because they convert the oil in your skin
into soap. An alkali turns red litmus paper blue.
 Alkalis are either strong or weak.
 Strong alkali is an alkali that ionizes completely when dissolved
in water producing high concentration of OH-(aq) in the solution.
For example Sodium Hydroxide
 Weak alkali is an alkali that dissociates partially giving low
concentration of OH-(aq) ions in the solution.
For example: Ammonium Hydroxide.
Acid and Alkalis
Amani Hamdi
Page 84
Some common alkalis and bases
Type
Alkali
Bases
Name
Formula
Ions
Strength
Sodium
hydroxide
NaOH
Na+, OH-
Strong
Potassium
hydroxide
KOH
K+, OH-
Strong
Ammonium
hydroxide
NH4OH
NH4+, OH-
Weak
Calcium Oxide
CaO
Don’t
ionize
strong
Magnesium
Oxide
MgO
Acid and Alkalis
Amani Hamdi
Page 85
Reactions of bases and alkalis
Reaction
Acid + base
salt + water
(neutralization)
Alkali +
ammonium salt
heating
Salt +
water +
ammonia
Alkali + fat
salt of fatty acids
( Soap)+ glycerol
Equation
Sulfuric acid + Magnesium Oxide
H2SO4 +
MgO
Sodium Hydroxide + Ammonium Chloride
NaOH(aq) +
NH4Cl(S)
NaOH(aq) + Oil
Observation
Magnesium Sulfate + water
MgSO 4
+ H2O
The
released
Sodium Chloride+ water+Ammonia ammonia
can be
tested using
NaCl(aq) + H2O(L) + NH3(g) damp red
litmus
paper, it
turns blue.
salt of fatty acids(soap) + glycerol
Acid and Alkalis
Amani Hamdi
Page 86
Oxides
when an element combines with oxygen, an oxide is formed.
Types of oxides
Metal oxides
Basic Oxides
Non-metal oxides
Acidic Oxides
Amphoteric
Neutral Oxide
Amani Hamdi
Acid and Alkalis
Page 87
Basic
Amphoteric
Examples
Most metal Oxides
(or hydroxides)
E.g: CaO , MgO ,FeO ,
Fe2O3, CuO ,etc.
ZnO
Al2O3
Most nonmetal Oxides
e.g: CO2, SO2,NO2, etc.
Acidic
Neutral
H2O
NO
CO


Type of oxide
Properties
 Ionic compound.
 Those that dissolve in water
produce alkalis.
 React with acids producing salt
and water Only (Neutralization
reaction)
 Ionic compounds.
 React with both acids alkalis.





Covalent Compounds.
Dissolve in water
Producing acids.
React with alkali
producing salt and water only
( Neutralization reaction)
 Do not react with acids.
 Covalent compounds.
 They neither react with acids
nor alkalis.
Amani Hamdi
Acid and Alkalis
Page 88
Indicators
 An indicator is used to detect whether a substance is acidic or
basic.
An indicator is a substance that changes colour when added to an
acid or to an alkali solution.
Some common indicators and their colour change
indicator
Litmus
phenolphthalein
Methyl orange
Thymophthalein
Acidic
medium
Red
Colorless
Red
Colorless
Neutral
medium
Purple
Colorless
Orange
Colorless
Alkaline
medium
Blue
Pink
Yellow
Blue
Universal Indicator(full-range indicator)
It gives range of colours (a spectrum) depending on the strength
of the acid or the alkali.
Note: solutions of the same acid but of different concentrations
give different colours.
Acid and Alkalis
Amani Hamdi
Page 89
The pH scale
It is a scale running from 0 to 14. Used for expressing the strength
of acids and alkalis.






Acids have pH less than 7.
The more acidic a solution, the lower the pH.
Neutral substances, such as pure water have a pH =7.
Alkalis have a pH greater than 7.
The more alkaline a solution, the higher its pH.
The pH of a solution can be measured using universal indicator
(solution or paper).
 More accurate method to measure the pH is to use a pH meter.
How the colour of universal indicator changes in solutions
of different pH values
Acid and Alkalis
Amani Hamdi
Page 90
Salt preparation
-Salts are ionic compounds made by neutralization of an acid with a
base (or alkali).
-To prepare a salt, you have to see if the salt is soluble or insoluble.
-The following diagram shows the solubility of various types of salts.
Preparing soluble salts
Salt Preparation
Amani Hamdi
Page 91
Note
 Salts including potassium , sodium & Ammonium ions are
soluble in water.
 All nitrate salts are soluble in water .
 All sulfate salts are soluble except pb , Ba & (Ca).
 All chloride salts are soluble except Pb and Ag .
 All carbonate salts are insoluble excepts Na , K and NH 4 .
 All Oxide and hydroxide salts are insoluble except Na , K ,
NH4 and (Ca)
Hydrated substance :
substance that is chemically combined with water
Anhydrous substance :
substance containing no water
Water of Crystallisation :
water molecules present in hydrated Crystals
CuSO4 .5 H 2O and CoCl2 . 6H 2O
Salt Preparation
Amani Hamdi
Page 92
Soluble salts can be prepared from their parent acids sing any of
the characteristic reactions of acids mentioned before:
Metal + Acid
salt + Hydrogen
Base + Acid
salt + water
Carbonate salt + Acid
salt + water + Carbon dioxide
There are two methods to prepare soluble salts
Method A:
This method is used to prepare a soluble salt from insoluble metal,
metal Oxide (base) or Carbonate salt.
Follow the following steps
1- Add excess (more than enough) of the solid (metal, metal
oxide or metal carbonate) to the acid. Excess solid is added to
make sure that all the acid is used up. The excess is seen at
the bottom.
2- The excess solid is removed by filtration.
3- The filtrate is gently evaporated till point of crystallization
and get a saturated solution .
4- The concentrated solution obtained is left to cool to
obtain crystals. The crystals are filtered off.
5- Crystals are dried carefully between two filter papers.
saturated solution : solution in which no more solute is
dissolved at certain temperature .
Salt Preparation
Amani Hamdi
Page 93
Remember to choose the suitable parent acid
Salt of
Chloride
Sulfate
Nitrate
Parent acid
Hydrochloric acid
Sulfuric acid
Nitric acid
Salt Preparation
Amani Hamdi
Page 94
Steps of preparing crystals of MgSO4.7H2O
1- Add excess
Mg
MgO
MgCO3
to the parent acid (Sulfuric acid)
In case of using the base MgO, you have to heat the acid to start
the reaction. No need to heat the acid if you use the metal or the
carbonate salt because they are readily to react with acid at room
temperature.
2- Filter to remove the excess Mg, MgO, MgCO3.
3- Half evaporate the filtrate till point of crystallization.
4- Leave to cool to get the crystals. Filter off the crystals.
5- Dry the crystals gently between two filter papers.
Generally
The solid added Is there a need to Reason
to the acid
heat the acid
Readily to
react at
Metal
No
room
temperature
To start the
Metal Oxide
Yes
reaction
Metal Carbonate
No
What shows that
the reaction stops
Bubbles stop
releasing.
Excess metal is seen
at the bottom.
Excess metal oxide
is seen at the
bottom.
Readily to Effervescence stops
react at
releasing.
room
The excess metal
temperature carbonate is seen at
the bottom.
Salt Preparation
Amani Hamdi
Page 95
Method B : Acid + Alkali by Titration
This method is used to prepare a soluble salt from a soluble base
(alkali) or carbonate.
Since both reactants are colourless and the alkali or the carbonate
are soluble, an indicator must be used.
Follow the following steps:
1- The acid is poured in a burette till its 0.0cm3. A known volume
of an alkali is delivered into a conical flask using a pipette. Drops
of an indicator are added for example Methyl Orange
2- The acid is run from the burette into the flask until the indicator
just changes colour. The volume of the acid ran into the flask is
recorded. The experiment is then repeated without using the
indicator using the known volume of the alkali used as well as
the recorded acid volume.
Note: instead of repeating the experiment, activated charcoal is
added to remove the indicator, and then the charcoal is filtered
off.
3- The salt solution is evaporated in the evaporating dish till point
of crystallization. Cool to form crystals. Filter off the crystals
from the remaining solution, wash with distilled water. Dry the
crystals gently between two filter papers.
Note : universal indicator is not used in titration as an
indicator as it gives a range of colors ,so the end point is not
sharp .
Salt Preparation
Amani Hamdi
Page 96
Steps of preparing crystals of Sodium Chloride from the
soluble base Sodium Hydroxide:
1- Fill a burette till its 0.0cm3 with Hydrochloric acid.
2- Deliver a known volume of Sodium Hydroxide in a conical
flask using a pipette.
3- Add drops of Methyl Orange to the flask. Methyl Orange is
yellow in alkaline media and orange in neutral ones.
4- Add the acid from the burette with regular shaking until the
colour changes from yellow to orange
5- Note the volume of acid used is for neutralization.
6- Repeat the experiment without the indicator using the same
volume of acid recorded as well as the alkali.
7- Evaporate the resulting solution in an evaporating dish till
point of crystallization.
8- Leave the concentrated solution to cool for the crystals to
form.
9- Filter off the crystals from the remaining solution.
Wash the crystals with distilled water.
10- Dry the crystals carefully between two filter papers.
Salt Preparation
Amani Hamdi
Page 97
Note :
Do not dry the crystals in an oven or by heating to avoid
dehydration ( losing water of crystallization)
The water of crystallization give the crystals their shape. In
some cases it also gives them their colour for example:
CuSO4.5H2O
heat
CuSO4
-5H2O
(blue hydrated salt)
(white anhydrous salt)
When hydrated salts are heated:
 Their water of crystallization driven off as steam.
 The crystals lose their shape and become powder.
 Sometimes the colour changes.
If the water is added again:
 The white anhydrous Copper(II)Sulfate changed to blue.(This
can be used as test for water).
 Heat is given off.
Salt Preparation
Amani Hamdi
Page 98
Preparation of insoluble salts
Insoluble salts are made by precipitation. Examples:
AgCl,BaSO4,PbI2
Steps of preparing Silver Chloride:
Before writing the steps let us select two reagents (chemicals used)
to prepare Silver Chloride.
Silver Chloride
Ag+
ClSelect a soluble ionic
compound containing Cl-, like
NaCl and make an aqueous
solution of NaCl.
Select a soluble ionic compound
Containing Ag+, like AgNO3And
make an aqueous solution of
AgNO3.
Steps :
1. Mix the two solutions of Silver Nitrate and Sodium Chloride, a
precipitate is formed (AgCl).
2. Filter off the precipitate to get it as residue.
3. Wash the residue with distilled water.
4. Dry the residue in an oven.
Salt Preparation
Amani Hamdi
Page 99
The equation for this reaction is:
Silver Nitrate + Sodium Chloride
Sodium Nitrate + Silverchloride
AgNO3(aq) + NaCl(aq)
NaNO3(aq) + AgCl(s)
The state symbol here is very important, it shows you the
precipitation
The equation can be simplified to show only those ions that
take part in the reaction and their products. The resulting
equation is called ionic equation.
How to write an ionic equation:
1- Write the equation with its state symbols
AgNO3(aq) + NaCl(aq)
AgCl(s) + NaNO3(aq)
2- Write a full ionic equation by separating the ions from the aqueous
compounds, as they are dissociated in the solutions.
Ag+(aq) + NO-3(aq) + Na+(aq) + Cl-(aq)
Na+(aq) + NO-3(aq) + AgCl(s)
 AgCl is insoluble so it will not dissociate into ions.
3- Cross the ions that remain unchanged, they are called spectator
ions.
Ag+(aq) + NO-3(aq) + Na+(aq) + Cl-(aq)
Na+(aq) + NO-3(aq) + AgCl(s)
4- Write the net ionic equations without the spectator ions.
Ag+(aq) +Cl-(aq)
AgCl(s)
Salt Preparation
Amani Hamdi
Page 100
State symbol
Symbol
S
l
g
aq
Meaning
solid
liquid
gas
Aqueous solution i.e. dissolved in water.
Write the net ionic equation of the following reaction
Equation:
Pb(NO3)2(aq) + 2KI(aq)
2KNO3(aq) + PbI2(s)
Full ionic equation:
Pb+2(aq) + 2NO3-(aq) + 2K+(aq) +2I-(aq)
2K+(aq) + 2NO3- + PbI2(s)
Net ionic equation:
Pb+2(aq)+2I-(aq)
PbI2(s)
Salt Preparation
Amani Hamdi
Page 101
Mixture separation and purification
-A mixture must be made of at least two substances, which may
be solid, liquid or gas. There are many ways in which the three
matter states can mix. If the states (solid, liquid or gases) are
completely mixed to become one phase, this mixture is called
solution. Example, the solid salt dissolves in liquid water to
produce a liquid mixture.
-The solid that dissolves in the liquid is the solute.
-The liquid in which the solid dissolves is called the solvent.
-In other types of mixture, the states remain separate. An
example of this type of mixture is a suspension of fine particles of
a solid in a liquid, such that we get in a precipitation reaction.
The most useful separation method for a particular mixture
depends on :
 The type of mixture
 The substance in the mixture we are interested in.
Types of mixtures
Mixture of solids
Mixture of solid
and liquid
Mixture of liquids Mixture of gases
Mixture separation and purification
Amani Hamdi
Page 102
Mixture of solids
A) Two solids one is soluble(A), the other is insoluble(B)
Steps of separation
 The mixture is delivered into a beaker.
 Add excess water to dissolve (A) and stir.
 Filter, the residue is B and the filtrate is A.
 Crystalize the filtrate to get solid crystals of A.
Note: Complete evaporation will produce powder of A.
B) Separating two solids one is magnetic, the other is
non-magnetic.
E.g. A mixture of Iron (magnetic) and Sulfur (non-magnetic).
Use a magnet to attract and separate iron from Sulfur.
C) Separating two solids, one can sublime.
E.g. A mixture of ammonium chloride and sodium chloride. By
heating, ammonium chloride sublimes leaving sodium chloride.
Mixture separation and purification
Amani Hamdi
Page 103
Mixture of a solid and a liquid
A) The solid is insoluble in the liquid.
E.g. Calcium Carbonate and water. The mixture can be separated
by filtration. The solid is the residue and the liquid is the filtrate.
Decantation Also can be used to separate a liquid from an
insoluble salt. Decantation is The process of removing a liquid
from a solid by pouring the liquid carefully .
B) The solid dissolved in the liquid.
-If you want to get the solid only, crystallize the solution.
E.g. CuSO4.5H2O crystals from aqueous CuSO4.
-If you want to get both liquid and solid, carry out simple
distillation.
Simple distillation: is the process of boiling a liquid and then
condensing the vapour produced back
into a liquid.
 A condenser is used to condense the
vapour into liquid. The liquid is
distillate.
 The process is also used to purify
liquids.
Mixture separation and purification
Amani Hamdi
Page 104
Mixtures of Liquids
Miscible Liquids
Immiscible Liquids
A) Separation of miscible liquids:
This separation is based on the fact that the liquids have different
boiling points. The process used is known as fractional distillation.
-The most volatile liquid (with
lower boiling point) in the
mixture distils over first and the
least volatile liquid (with higher
boiling point) distils over last.
E.g. a mixture of ethanol and
water.
Ethanol boils at 78⁰C whereas
water boils at 100⁰C. Ethanol
distils first and collected then
water.
-Liquefied air is separated by fractional distillation.
-Petroleum also is separated by the same technique.
-The fractionating column has glass beads in the column to
provide a large surface area for condensation.
Mixture separation and purification
Amani Hamdi
Page 105
B) Separation of immisble liquids
The process of separation depends on the different densities of
liquids.
E.g. a mixture of water and oil.
Oil has less density than water.
 Separating funnel is used to
separate such mixtures.
 The lower (denser) layer is tapped
off at the bottom.
 This type of separation is used in
industry. E.g. in the blast furnace,
the molten slag forms a separate
layer on top of molten iron. The two
layers can then be tapped off
separately.
Mixture of Gases
Mixture of gases can be separated either by:
A) Diffusion:
This way depends on the difference in Mr of the molecules of the
gases. The one that has less Mr diffuses faster.
B) Fractional distillation of Liquefied mixture of gase:s
This way depends on the difference in boiling points. E.g.
Components of air can be separated by fractional distillation of
liquefied air.
Mixture separation and purification
Amani Hamdi
Page 106
Separating coloured solids dissolved in a solvent
by chromatography
E.g. Separation of the colours present in a dye in ink.
To separate using chromatography follow the following steps:
1. Get a chromatography paper.
2. Draw a line with a pencil (insoluble in solvents) called base line. Do not
use ink.
3. Put a drop of the sample on the base line using a glass rod.
4. Put the paper in a suitable solvent .The level of solvent must start below
the sample to prevent the solubility of the spot in the solvent.
5. Leave the chromatogram for several hours. Spots of several colours are
separated.
base line
A drop of dye
solvent
Solvent front
3 separated
sports
Mixture separation and purification
Amani Hamdi
Page 107
Notes:
 Substances separate according to their solubility in the solvent. The dyes
are carried by the solvent and begin to separate. The substance that is
most soluble moves the fastest up the paper.
 An insoluble substance will remain at the origin.
 The run stops just before the solvent front (the level reached by the
solvent).
 If the separated substances are colourless, the paper is treated with
locating agent that reacts with the samples to produce coloured spots
e.g Amino acids are colourless, a locating agent is used.
Note : Molecules of amino acids can also be viewed under ultra violet
light.
The purity and identity of substances:
The distance moved by a particular spot is measured and related to the
position of the solvent front.
The ratio of these distances is called rate of flow (Rf )value. This value is
used to identify the substance:
Rf =
Distance moved by the sample
Distance moved by the solvent
 Paper chromatography is one test that can be used to check the Purity
of a substance. If the sample is pure, it should give one spot by
chromatography.
 The identity of substances can also be checked by comparing its Rf value
to that of a pure sample of the same substance.
Mixture separation and purification
Amani Hamdi
Page 108
Practical work
Safety
precautions









Never run around the laboratory.
Never drink or eat in the laboratory.
Wear safety goggles.
Wear white coat.
Tie hair.
Make sure where the fire extinguishers are and how to use them.
Never taste any chemicals in the laboratory.
Never handle chemicals with your fingers ( use clean dry spatula ).
Use a fume cupboard in lab or well ventilated lab if harmful
gases are produced like halogens.
 Don’t heat alcohols directly on the Bunsen burner but use water bath.
Chemical warnings and signs:
Explosive
These substances may explode if ignited in air or
exposed to heat. A sudden shock or friction may
also start an explosion. Particular care should be
taken in warm climates.
Oxidizing
These substances produce much heat as they react
with other materials. They can create a fire risk. They
will react with organic substances such as wood.
Practical
work
Amani
Hamdi
Page 109
Highly flammable
These are solids, liquids or gases that may easily
catch fire in a laboratory under normal conditions.
Poisonous
These substances are a serious risk to health. Some
can cause death. These chemicals can affect you if
you swallow them, inhale them, or absorbed through
the skin. They should be stored in a locked cupboard.
Harmful
These chemicals are less of a health risk than
poisonous substances, but they must be handled
with care.
Corrosive
These chemicals destroy living tissues, including
eyes and skin. If they are spilt on your skin, you
should wash the exposed area with plenty of water.
Irritant
These substances are not corrosive but they can cause
reddening of the skin. The effect may be immediate or
it may only be observed after prolonged, or repeated
contact with the chemical.
Radioactive
The radioactive chemicals used in schools have low
activity. They are normally only used by teachers, for
demonstrations. They should be treated in the same
way as poisonous substances.
Practical
work
Amani
Hamdi
Page 110
Lab equipment:
Test tube holds
liquids/solids
Beaker
holds
liquids
Funnel for
pouring/filtering
Boiling
tube for
heating
liquids
Triangle
support
for
crucible
Beehive
shelf for
collecting
gas over
water
Dropper for
measuring
small volumes
of liquid
Burette for
measuring
large exact
volume of
liquid
Crucible for
heating solids
to high
temperature
Gas jar to
collect
gases
Practical
work
Amani
Hamdi
Page 111
Gauze
spreads heat
under a flask
Measuring
cylinder
for
measuring
liquids
Tripod
supports
beaker,
crucible
etc…
over
flame
Evaporating
dish for
evaporating
solutions
Gas syringe
for measuring
volume of
gases
Round
bottom
flask
for
heating
liquids
Pipette for
delivering
exact volume
of liquid
Conical
flask to
hold
liquids
Tap funnel for
separating
immiscible
liquids
Tong to
hold
objects
Practical
work
Amani
Hamdi
Page 112
Condenser for
condensing
vapour
Spatula
for
transferring
solids
Mortar
and pistil
for
grinding
large solid
substances
Stand
supports
flask, tube
etc… in
complex
apparatus
Improvements for more accurate experimental results:
 Use Styrofoam (polystyrene) cup or insulated cups in
experiments that are involved in heat change.
 Burette is used to measure the volume of solution added
accurately rather than measuring cylinder.
 Pipette delivers a fixed volume accurately rather than
measuring cylinder.
Practical
work
Amani
Hamdi
Page 113
Methods of collecting gases
1) Downward delivery is used for gases that areser
den than air such as: Chlorine, Hydrogenbo
Chloride, Car dioxide, Sulfur dioxide andn
Nitrogen dioxide.
2) Upward delivery is used for gases that are
less dense than air such as Ammonia and
Hydrogen.
3) Collection over water is used for gases
that are not very soluble in water such as:
Hydrogen, Oxygen and Nitrogen.
4) Collection in a gas syringe is
useful when volume of gas
needs to be measured.
Practical
work
Amani
Hamdi
Page 114
Danger of “back suction”
The problem arises when heating is stopped before delivery tube is
removed from water. The reduced pressure in the reaction tube as it
cools; results in the cold water can be sucked back into the hot boiling
tube. The tube will crack and an explosion may occur.
“Sucking back” can be prevented by making sure that the delivery tube is
removed first before heating is stopped.
Practical
work
Amani
Hamdi
Page 115
Functions of ceramic wool
1) To hold liquids.
Delivery
tube
2) Act as a separator.
3) Act as filter to
prevent spreading
of the reactants
contaminating the
rest of the
apparatus.
Practical
work
Amani
Hamdi
Page 116
Methods of drying gases:
1) Conc. Sulfuric acid is used to dry all gases except ammonia.
2) Anhydrous calcium chloride is used for all gases except
ammonia, which forms a complex with calcium chloride.
3) Calcium oxide is used to dry ammonia and neutral gases.
Practical
work
Amani
Hamdi
Page 117
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