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Chemistry

Atom and Periodic Table of Element

For Grade X

By:
Widy Alif Putra Said
4301412095

Semarang State University


2015

Basic Competency

3.2

Analyzing the development of atomic model.

3.3

Analyzing the atomic particles based on Bohr atomic theory and Mechanical Quantum
theory.

3.4

Analyzing the relationship electron configuration and orbital diagram to determine the
position of element in periodic table and element periodic prroperties.

4.2

Processing and analyzing the development of atomic model.

4.3

Processing and analyzing the atomic particles based on Bohr atomic theory and
Mechanical Quantum theory.

4.4

Providing the result of analyzing the relationship electron configuration and orbital
diagram to determine the position of element in periodic table and element periodic
properties.

Indicators
1.
2.
3.
4.
5.
6.
7.
8.

Comparing the development of element periodic table to identify its majority and minority.
Explaining basic of grouping elements.
Determining basic particles (proton, electron and netron).
Determining electron configuration and valence electron.
Determining atomic relative mass based on periodic table.
Grouping the element into isotop, isobar and isoton.
Grouping the element into metal, non metal and metaloid.
Analyzing table, graphik to determine regularity of atomic radius, ionization energy, electron
affinity and electronegativity.

Atomic Theory Development

1. Democritus

460 BC - Greek philosopher proposes the existence of the atom

He pounded materials until he made them into smaller and smaller parts

He called them atoma which is Greek for indivisible.


His Theory:
All atoms:

Are small hard particles

Are made of a single material formed into different shapes and sizes

Are always moving, and they form different materials by joining together

2. John Dalton
Dalton's atomic theory contains five basic assumptions:

All matter consists of tiny particles called atoms. Dalton and others imagined the atoms
that composed all matter as tiny, solid spheres in various stages of motion.

Atoms are indestructible and unchangeable. Atoms of an element cannot be created,


destroyed, divided into smaller pieces, or transformed into atoms of another element.
Dalton based this hypothesis on the law of conservation of mass as stated by Antoine
Lavoisier and others around 1785.

Elements are characterized by the weight of their atoms. Dalton suggested that all atoms
of the same element have identical weights. Therefore, every single atom of an element
such as oxygen is identical to every other oxygen atom. However, atoms of different
elements, such as oxygen and mercury, are different from each other.

In chemical reactions, atoms combine in small, whole-number ratios. Experiments that


Dalton and others performed indicated that chemical reactions proceed according to atom
to atom ratios which were precise and well-defined.

When elements react, their atoms may combine in more than one whole-number ratio.
Dalton used this assumption to explain why the ratios of two elements in various

compounds, such as oxygen and nitrogen in nitrogen oxides, differed by multiples of each
other.
John Dalton's atomic theory was generally accepted because it explained the laws of
conservation of mass, definite proportions, multiple proportions, and other observations.
Although exceptions to Dalton's theory are now known, his theory has endured reasonably well,
with modifications, throughout the years.

3. J J. Thomson
1897 - English chemist and physicist; discovered 1st subatomic particles

Plum Pudding Model or


Raisin Bun Model
Proposed by J.J.
Thomson
His Theory:
o Atoms contain negatively charged particles called electrons and positively
charged matter.
o Created a model to describe the atom as a sphere filled with positive matter with
negative particles mixed in
Referred to it as the plum pudding model

4. Ernest Rutherford

1912 - New Zealand physicist discovered the nucleus

Nuclear Model
Proposed by Ernest
Rutherford

His Theory:

Small, dense, positively charged particle present in nucleus called a proton

Electrons travel around the nucleus, but their exact places cannot be described.

5. Niels Bohr Atomic Models


Bohr atomic model suggests that the atom consists of a
nucleus is very small and is surrounded by a positively
charged electron has a negative charge that orbits

This is the picture theory Bohr model of the atom.

Figure 1. Bohr Atom Model


Niels Bohr Bohr's atomic theory put forward in 1915. Due to the Bohr model of the atom
is a modification (development) of the Rutherford atomic model, some chemists call the
Rutherford-Bohr theory of the atom. Although Bohr's atomic theory had been developed, but in
fact the Bohr model of the atom still has weaknesses. However, some points of the Bohr model
of the atom can be accepted. Unlike Dalton's atomic theory and atomic theory of Rutherford,
Bohr atomic theory excellence can explain the Rydberg constant for hydrogen line emission
spectra. That's one of the advantages Niels Bohr atomic theory.
Bohr atomic model shaped like a solar system, with electrons which are in circulation
path (orbit) around the positively charged nucleus is very small in size.
The force of gravity in the solar system can be illustrated mathematically as the Coulomb
force between a nucleus (nuclei) are positively charged with negatively charged electrons.
The sound of the Bohr atomic theory postulates
Bohr atomic theory can be explained as follows:
1. Electrons circling the atomic nucleus in specific orbits were circular. These orbits are
often referred to as electron shells are represented by the notation K, L, M, N ... etc
that are berututan accordance with n = 1, 2, 3, 4 ... and so on.
2. Electrons in each orbit has a higher specific energy with the increasing size of the
growing circular orbit or the value of n. This energy is quantized and prices permitted
by the stated price quantized angular momentum of electrons n (h/2) with n = 1, 2, 3,
4 ... and so on.
3. During the orbit, the electron does not radiate energy and said in a stationary state.
The existence of a stationary electron in orbit is maintained by the force of
electrostatic attraction of electrons by atomic nuclei is balanced by the centrifugal
force of the motion of electrons.
4. Electrons can move from one orbit to another orbit which has a higher energy when
the electrons absorb energy in accordance with the magnitude of the energy difference
between the two orbits is concerned, and vice versa when the electrons move into an
orbit that has a lower energy would emit radiation energy line spectra are observed as

the magnitude corresponding to the energy difference between the two orbits is
concerned.
5. Atoms in a molecule is said in the state of the ground level (ground state) when the
electrons occupy orbits so as to give the lowest total energy. And when the electrons
occupy orbits which gives a higher energy than the energy levels of atoms in
essentially said the excited level (excited state). Atoms in the ground state is more
stable than in the excited state.
Model Hidrogen Bohr
The simplest example of the Bohr model of the hydrogen atom (Z = 1) or a hydrogen-like
ions (Z> 1), which has negatively charged electrons surround the positively charged nucleus.
Electromagnetic energy is absorbed or released when an electron moves from one track to
another track. The radius of the track increases as n2, where n is the principal quantum number.
Transition from 3 to 2 produces the first line of the Balmer series. For hydrogen (Z = 1) will
produce a photon with a wavelength of 656 nm (red light).
Weakness Bohr Atomic Theory
Although considered to be a revolutionary, but still found weaknesses Bohr atomic theory
are:

Breaking the Heisenberg uncertainty principle because the electron has a radius and a
known trajectory.

Bohr atomic model has a value of the angular momentum of the ground state trajectory is
wrong.

Weak explanation of atomic spectra predicted greater.

Unable to predict the relative intensities of the spectral lines.

Bohr atomic model can not explain the structure of the spectral lines are well.

Unable to explain the Zeeman effect.

6. Quantum Mechanics Model of the Atom


An explanation of a more complete atomic structure necessary to know more details
about the structure of electrons in the atom. Complete atomic model should be able to explain the
mystery of the Zeeman effect and is suitable for many electron atoms. Two of these symptoms
can not be explained by the Bohr model of the atom.
Effect Zeeman
Atomic line spectrum is observed when an electric current is passed through gas in a tube
of gas prod. Additional lines observed in the emission spectrum when excited atoms placed in an
external magnetic field. One line in the spectrum of visible emission lines as three lines (with
two additional lines) in the spectra of atoms when placed in a magnetic field. Breaking up a line
into multiple lines in a magnetic field is known as the Zeeman effect.

Figure 2. Separation of atomic spectral lines in a magnetic field


Zeeman effect can not be explained using the Bohr model of the atom. As such, required
a more complete model of the atom and the more general to explain the Zeeman effect and the
spectrum of many electron atoms.
Model Atomic model of Quantum Mechanics
Previously we have discussed about the wave-particle duality which states that an object
can behave either as a wave or a particle. the atomic scale, the electrons can be reviewed as a
wave phenomenon that does not have a particular position in space. The position of an electron is
represented by a probability or chance of finding the electron in the largest space.

To get a complete and general description of the structure of the atom, the wave-particle
duality principle used. Here the electron motion is described as a wave phenomenon. Newton's
equation of dynamics that was originally used to describe the motion of electrons is replaced by
the Schrodinger equation for the wave function of the electron states. Atomic model which is
based on this principle is called the atomic model of quantum mechanics.

Figure 3. Atomic model of quantum mechanics


To further investigate the structure, we need to know a term called the "quantum number".
There are four types of quantum numbers, is;
1.
2.
3.
4.

First Quantum Numbers (n)


Quantum Numbers Azimuth (l)
Magnetic Quantum Numbers (m)
The spin quantum number (s)

First Quantum Numbers (n)


Is a number that states the energy level or shell electrons are:
Shells number

Shells

Total electron max


(2n)2

(n=1)

2(1)2 = 2

(n=2)

2(2)2 = 8

(n=3)

2(3)2 = 18

(n=4)

2(4)2 = 32

Quantum Numbers Azimuth (l)


Numbers stating the location of a subshell

Shell number

Shell

Value subshell

Subshell

(n=1)

(n=2)

0, 1

(n=3)

0, 1 ,2

(n=4)

0, 1, 2, 3

subshell

Number of Orbital

Magnetic Quantum Numbers (m)


Numbers stating it was the location of an orbital
Subshell

value (m)

-1,0,+1

-2,-1, 0, +1, +2

-3, -2,-1, 0 +1, +2, +3

Spin Quantum Numbers


Spin quantum number is needed to explain the anomalous Zeeman effect. This anomaly in the
form of splitting of spectral lines into more lines than expected. If the Zeeman effect is caused by
the presence of an external magnetic field, the anomalous Zeeman effect caused by the rotation
of the electron on its axis. Rotation or spin of electrons produces an intrinsic angular momentum

of electrons. Spin angular momentum also has two different orientations, namely spin up and
spin down. Each electron spin orientations have different energies thin so it looks as separate
spectral lines of atoms in the magnetic field derived from the electron spin.

Electron spin quantum number is represented by a separate so-called magnetic spin quantum
number (or so-called spin only). Value of the spin quantum number should only be one of two
values + or - . ifmsadalah spin quantum number, angular momentum components of the zaxis direction is written as

Spin up is expressed with

Spin down is expressed with

Periodic Table of Element Development

Chemists have always looked for ways of arranging the elements to reflect the
similarities between their properties. The modern periodic table lists the elements in order of
increasing atomic number (the number of protons in the nucleus of an atom). Historically,
however, relative atomic masses were used by scientists trying to organise the elements. This was
mainly because the idea of atoms being made up of smaller sub-atomic particles (protons,
neutrons and electrons) had not been developed. Nevertheless, the basis of the modern periodic
table was well established and even used to predict the properties of undiscovered elements long
before the concept of the atomic number was developed.

Table formation
Ask most chemists who discovered the periodic table and you will almost certainly get
the answer Dmitri Mendeleev. Certainly Mendeleev was the first to publish a version of the table
that we would recognise today, but does he deserve all the credit?
A number of other chemists before Mendeleev were investigating patterns in the properties of the
elements that were known at the time. The earliest attempt to classify the elements was in 1789,
when Antoine Lavoisier grouped the elements based on their properties into gases, non-metals,
metals and earths. Several other attempts were made to group elements together over the coming
decades. In 1829, Johann Dbereiner recognised triads of elements with chemically similar
properties, such as lithium, sodium and potassium, and showed that the properties of the middle
element could be predicted from the properties of the other two
It was not until a more accurate list of the atomic mass of the elements became available at a
conference in Karlsruhe, Germany in 1860 that real progress was made towards the discovery of
the modern periodic table.

This area of the website celebrates the work of many famous scientists whose quest to learn more
about the world we live in and the atoms that make up the things around us led to the periodic
table as we know it today.

Alexandre-Emile Bguyer de Chancourtois

Alexandre Bguyer de Chancourtois. Reproduced courtesy of Annales des mines, Paris.


Can France claim the first periodic table? Probably not, but a French Geology Professor
made a significant advance towards it, even though at the time few people were aware of it.
Alexandre Bguyer de Chancourtois was a geologist, but this was at a time when
scientists specialised much less than they do today. His principal contribution to chemistry was
the 'vis tellurique' (telluric screw), a three-dimensional arrangement of the elements constituting
an early form of the periodic classification, published in 1862.
The telluric screw plotted the atomic weights of the elements on the outside of a cylinder,
so that one complete turn corresponded to an atomic weight increase of 16. As the diagram
shows, this arrangement means that certain elements with similar properties appear in a vertical
line. Although the telluric screw did not correctly display all the trends that were known at the
time, de Chancourtois was the first to use a periodic arrangement of all of the known elements,
showing that similar elements appear at periodic atom weights.

The vis tellurique from De Chancourtoiss original publication (right) and a copy drawn out with modern symbols (left).

John Newlands

John Newlands. Reproduced courtesy of the Library and Information Centre, Royal Society of
Chemistry.
John Newlands was British; his father was a Scottish Presbyterian minister. He was
educated by his father at home, and then studied for a year (1856) at the Royal College of

Chemistry, which is now part of Imperial College London. Later he worked at an agricultural
college trying to find patterns of behaviour in organic chemistry. However, he is remembered for
his search for a pattern in inorganic chemistry.
Just four years before Mendeleev announced his periodic table, Newlands noticed that
there were similarities between elements with atomic weights that differed by seven. He called
this The Law of Octaves, drawing a comparison with the octaves of music. The noble gases
(Helium, Neon, Argon etc.) were not discovered until much later, which explains why there was
a periodicity of 7 and not 8 in Newlands table. Newlands did not leave any gaps for
undiscovered elements in his table, and sometimes had to cram two elements into one box in
order to keep the pattern. Because of this, the Chemical Society refused to publish his paper,
with one Professor Foster saying he might have equally well listed the elements alphabetically.
Even when Mendeleev had published his table, and Newlands claimed to have discovered
it first, the Chemical Society would not back him up. In 1884 he was asked to give a lecture of
the Periodic Law by the Society, which went some way towards making amends. Finally, in
1998 the Royal Society of Chemistry oversaw the placing a blue commemorative plaque on the
wall of his birthplace, recognising his discovery at last.

Julius Lothar Meyer

Julius Lothar Meyer . Reproduced courtesy of the Library and Information Centre, Royal Society
of Chemistry.
Meyer trained at Heidelberg University under Bunsen and Kirchhoff, as did Mendeleev.
So the two scientists would certainly have known each other although neither was aware of all
the work done by the other. Meyer's roots, however, were firmly in Germany. Meyer was just
four years older than Mendeleev, and produced several Periodic Tables between 1864-1870.
His first table contained just 28 elements, organised by their valency (how many other
atoms they can combine with). These elements were almost entirely main group elements, but in
1868 he incorporated the transition metals in a much more developed table. This 1868 table
listed the elements in order of atomic weight, with elements with the same valency arranged in
vertical lines, strikingly similar to Mendeleevs table. Unfortunately for Meyer, his work wasnt
published until 1870, a year after Mendeleevs periodic table had been published. Even after
1870, Meyer and Mendeleev were still unaware of each others work, although Meyer later
admitted that Mendeleev had published his version first.
Meyer did contribute to the development of the periodic table in another way though. He
was the first person to recognise the periodic trends in the properties of elements, and the graph
shows the pattern he saw in the atomic volume of an element plotted against its atomic weight.

Dmitri Mendeleev

Dmitri Mendeleev. Reproduced courtesy of the Library and Information Centre, Royal Society of
Chemistry.
As we have seen, Mendeleev was not the first to attempt to find order within the
elements, but it is his attempt that was so successful that it now forms the basis of the modern
periodic table.
Mendeleev did not have the easiest of starts in life. He was born at Tobolsk in 1834, the
youngest child of a large Siberian family. His father died while he was young, and so his mother
moved the family 1500 km to St. Petersburg, where she managed to get Dmitri into a good

school, recognising his potential. In his adult life he was a brilliant scientist, rising quickly in
academic circles. He wrote a textbook, Chemical Principles, because he couldnt find an
adequate Russian book.
Mendeleev discovered the periodic table (or Periodic System, as he called it) while
attempting to organise the elements in February of 1869. He did so by writing the properties of
the elements on pieces of card and arranging and rearranging them until he realised that, by
putting them in order of increasing atomic weight, certain types of element regularly occurred.
For example, a reactive non-metal was directly followed by a very reactive light metal and then a
less reactive light metal. Initially, the table had similar elements in horizontal rows, but he soon
changed them to fit in vertical columns, as we see today.
Not only did Mendeleev arrange the elements in the correct way, but if an element
appeared to be in the wrong place due to its atomic weight, he moved it to where it fitted with the
pattern he had discovered. For example, iodine and tellurium should be the other way around,
based on atomic weights, but Mendeleev saw that iodine was very similar to the rest of the
halogens (fluorine, chlorine, bromine), and tellurium similar to the group 6 elements (oxygen,
sulphur, selenium), so he swapped them over.
The real genius of Mendeleevs achievement was to leave gaps for undiscovered
elements. He even predicted the properties of five of these elements and their compounds. And
over the next 15 years, three of these elements were discovered and Mendeleevs predictions
shown to be incredibly accurate. The table below shows the example of Gallium, which
Mendeleev called eka-aluminium, because it was the element after aluminium. Scandium and
Germanium were the other two elements discovered by 1886, and helped to cement the
reputation of Mendeleevs periodic table.
The final triumph of Mendeleevs work was slightly unexpected. The discovery of the
noble gases during the 1890s by William Ramsay initially seemed to contradict Mendeleevs
work, until he realised that actually they were further proof of his system, fitting in as the final
group on his table. This gave the table the periodicity of 8 which we know, rather than 7 as it had

previously been. Mendeleev never received a Nobel Prize for his work, but element 101 was
named Mendelevium after him, an even rarer distinction.

Eka-aluminium (Ea)

Gallium (Ga)

Atomic weight

About 68

69.72

Density of solid

6.0 g/cm

5.9 g/cm

Melting point

Low

29.78C

Valency

Method of discovery

Probably from its spectrum

Spectroscopically

Formula Ea2O3, density 5.5 Formula Ga2O3, density 5.88


Oxide

g/cm3. Soluble in both acids g/cm3. Soluble in both acids and


and alkalis

alkalis

A comparison of Mendeleevs predicted Eka-aluminium and Gallium, discovered by Paul


Emile Lecoq in 1875

Henry Moseley

Henry Moseley. Reproduced courtesy of the Library and Information Centre, The Royal Society
of Chemistry.
It wasnt until 1913, six years after Mendeleevs death that the final piece of the puzzle
fell into place. The periodic table was arranged by atomic mass, and this nearly always gives the
same order as the atomic number. However, there were some exceptions (like iodine and

tellurium, see above), which didnt work. Mendeleev had seen that they needed to be swapped
around, but it was Moseley that finally determined why.
He fired the newly-developed X-ray gun at samples of the elements, and measured the
wavelength of X-rays given. He used this to calculate the frequency and found that when the
square root of this frequency was plotted against atomic number, the graph showed a perfect
straight line. Hed found a way to actually measure atomic number. When the First World War
broke out, Moseley turned down a position as a professor at Oxford and became an officer in the
Royal Engineers. He was killed by a sniper in Turkey in August 15, and many people think that
Britain lost a future Nobel prize winner.
Within 10 years of his work, the structure of the atom had been determined through the
work of many prominent scientists of the day, and this explained further why Moseleys X-rays
corresponded so well with atomic number. The idea behind the explanation is that when an
electron falls from a higher energy level to a lower one, the energy is released as electromagnetic
waves, in this case X-rays. The amount of energy that is given out depends on how strongly the
electrons are attracted to the nucleus. The more protons an atom has in its nucleus, the more
strongly the electrons will be attracted and the more energy will be given out. As we know,
atomic number is also known as proton number, and it is the amount of protons that determine
the energy of the X-rays.
After years of searching, at last we had a periodic table that really worked, and the fact
that we still use it today is testament to the huge achievement of these and many other great
minds of the last two centuries of scientific discovery.

Periodic Table of Element


Period - A horizontal row in the periodic table.
The energy levels of the s and p orbitals are numbered by the row in which they are located.
e.g. The 2s orbital is in the second row (Li and Be) and the 3p orbitals are in the third row (Al,
Si, P, S, Cl, Ar)

The d orbitals are placed one row below their energy level.
e.g. The 3d orbitals are in the fourth row

Group - A vertical column, or family, in the periodic table.


Numbered in two ways:

8 9

II

III

IV

VI

VII

VIIIB

12

13

14

15

16

17

18

II

III

IV

VI

VII

VIII

Li Be

Ca Sc Ti

Cr

Sr

Zr

Nb

Mo Tc

Ru

Rh

Cs Ba La Hf

Ta

Re

Os

Ir

R
b

Fr Ra

N O F

Al Si P

Mn Fe

Co

Un

Un

Un

Un Un

Un

N C

Zn

Pt

C
l

A S

In Sn

S
b

Tl Pb Bi

Te I

N
e
Ar

Kr
X
e

A R

Group 1 (IA) - Alkali Metals (excluding H)


1. Li (lithium), Na (sodium), K (potassium), Rb (rubidium), Cs (cesium), and Fr (francium)
All form hydroxides (e.g. NaOH)
2. All are active metals
3. Activity
increases
as
you

move

down

the

column

React violently when they come into contact with water


4. All have one valence electron
Li:

[He] 2s1

Rb:

[Kr] 5s1

Na:

[Ne] 3s1

Cs:

[Xe] 6s1

K:

[Ar] 4s1

Fr:

[Rn] 7s1

5. All lose one electron to form cations with a charge of +1 e.g. Li+, Na+, and K+

Group 2 (IIA) - Alkaline Earth Metals


1. Be (beryllium), Mg (magnesium), Ca (calcium), Sr (strontium), Ba (barium), and Ra
(radium)
All but Be and Mg are active metals
2. Activity
increases
as
you

move

down

the

column

Ca, Sr, and Ba react violently when they come into contact with water
3. All have two valence electrons
Be:

[He] 2s2

Sr:

[Kr] 5s2

Mg:

[Ne] 3s2

Ba:

[Xe] 6s2

Ca:

[Ar] 4s2

Ra:

[Rn] 7s2

4. Tend to lose two electrons to form cations with a charge of +2 e.g. Be2+, Mg2+, and Ca2+
Alkaline earth metals are less active than their adjacent alkali metals e.g. Be is less active
than Li; Mg is less active than Na

Groups 3-12 (IIIB - VIIIB, IB & IIB) - Transition Metals

1. All

have

valence

electrons

in

the

orbitals

Form compounds in which they have various oxidation numbers


2. Ag
(silver)
generally
forms
Ag+
(+1
oxidation

state)

Zn (zinc) generally forms Zn2+ (+2 oxidation state)


3. Brass is an alloy of copper and zinc

Group 13 (IIIA)
1. B (boron) - only element in the group that is not a metal; has semimetal and nonmetal
characteristics.
Al (aluminum) - fairly active metal, third most abundant in the earth's crust.
2. Loses three electrons to form Al3+
3. Forms compounds in which it has an oxidation state of +3
4. Other metals - Ga (gallium), In (indium), and Tl (thallium) - very scarce active metals

Group 14 (IVA)
1. C (carbon) - nonmetal
2. Elemental forms of carbon include:
Graphite (crystalline) - Strong bonds between atoms within planes resulting in extremely
high melting and boiling points. Weaker bonds connecting the planes which account for
the soft texture of graphite.
Diamond (crystalline) - Hardest naturally occurring substance with extremely high
melting and boiling points. Atoms arranged in a tetrahedral array with strong C-C bonds.
Charcoal - Results from heating wood without oxygen present
Coke (amorphous) - More structured than other amorphous forms of carbon; made from
coal.
Carbon Black (amorphous) - Formed by burning natural gas or other carbon compounds
in a limited amount of air
3. Has strong C-C single bonds, C=C double bonds, and C C triple bonds.
Forms
4.
5.
6.
7.

covalent

bonds

with

other

Can form double and triple bonds with other nonmetals


S (silicon) and Ge (germanium) - semimetals
Silicon is the second most abundant element in the earth's crust
Sn (tin) and Pb (lead) - less reactive metals
Both form compounds in which their oxidation states
Bronze is an alloy of tin and copper

elements

are

+2

or

+4

Group 15 (VA)
1. N (nitrogen) and P (phosphorus) - nonmetals
2. Nitrogen is found in its elemental form at room temperature as a diatomic gas (N 2).
Nitrogen makes up approximately 80% of earth's atmosphere by volume.
In

compounds,

the

oxidation

of

nitrogen

can

range

from

-3

to

+5.

Haber process - mixing N2 and H2 gases at 200 to 300 atm and 400 C to 600 C over a
finely

divided

iron

catalyst

to

produce

NH3

Pure elemental phosphorus is white phosphorus (P 4). It is highly reactive and combusts
with

air

at

room

temperature

but

is

unreactive

with

water.

Red phosphorus is formed when white phosphorus is heated and is much less reactive
than

white

phosphorus.

Phosphorus can expand its valence (outermost) shell to hold more than eight electrons
(can

store

N N

extra

triple

electrons

bonds

are

in
much

the

3d

stronger

P-P single bonds are stronger than N-N single bonds.


3. As
(arsenic)
and
Sb
(antimony)

orbitals).
than

P P.

semimetals

Bi (bismuth) - metal

Group 16 (VIA)
1. (oxygen), S (sulfur), and Se (selenium) - nonmetals
2. Oxygen is the most abundant element on earth, making up approximately 45% of the
earth's crust (by weight), 85% of the oceans (by weight) and 20% of the atmosphere (by
volume).
Oxygen is generally diatomic (O2) in its elemental form, but ozone (O3) is an allotrope of
O2.
3. At

concentrations

above

ppm,

ozone

is

toxic.

Ozone can absorb ultraviolet (UV) radiation from the sun, and serves as a filter in the
atmosphere.
4. Oxygen is

very

strong

oxidizing

agent,

weaker

Oxygen generally takes on a -2 oxidation number in compounds.

only

to

fluorine.

5. In peroxide (O22-), oxygen has a -1 oxidation number, e.g. H2O2, hydrogen peroxide.
6. Elemental sulfur is a yellow solid at room temperature with a cyclical molecular structure
(S8).
O=O

double

S-S

bonds

single

are

bonds

much

stronger

are

stronger

than

S=S

than

double
O-O

bonds.
bonds.

Sulfur can expand its valence (outermost) shell, to hold more than eight electrons (can
store

extra

electrons

in

the

3d

orbitals).

In compounds, sulfur can have oxidation numbers ranging from -2 to +6.


The prefix thio- is given to compounds in which an S atom replaces an O atom.
7. Te (tellurium) and Po (polonium) - semimetals

Group 17 (VIIA) - Halogens


1. F

(fluorine),

All

are

All

Cl

(chlorine),

nonmetals
are

Br

(bromine),

except

diatomic

for
in

At
their

(iodine),
which

and At

is

semimetal

elemental

All gain one electron to form anions with a charge of -1.


2. e.g. F-, Cl-, and Br3. In compounds, their oxidation numbers range

from

(astatine)
form

-1

to

+7.

None are found in nature in their elemental forms; instead they are found as salts of the
halide

ions.

Properties (at room temperature)


4. F2 - highly toxic, colorless gas, most reactive element known.
5. So reactive that it can even form compounds with noble gases (once thought to be inert)
Used
6.
7.
8.
9.

in

manufacturing

Teflon,

(C2F4)n

Used to make freons which are used in refrigerators


Cl2 - highly toxic, pale yellow-green gas, strong oxidizing agent
Used commercially as a bleaching agent an as a disinfectant
Br2 - reddish-orange liquid with a bad odor
Its name, bromine, is derived from the Greek bromos which means "stench"
Used in preparing fire-extinguishing agents, sedatives, insecticides, and antiknock agents

for gasoline
10. I - deep purple solid with a metallic-like luster
11. Sublimes directly into a violet gas (I2) from the solid phase when heated without passing
through

the

liquid

phase

Used

as

AgI

(silver

disinfectant,
iodide)

catalysts,
is

drugs,

used

and

in

dyes

photography

Iodine deficiency in the human body can lead to a goiter, a swelling of the thyroid gland.

Group 18 (VIIIA) - Noble (Rare) Gases


1. He (helium - "sun"), Ne (neon - "new one"), Ar (argon - "lazy one"), Kr (krypton "hidden

one"),

Xe

(xenon

"stranger"),

and

Rn

(radon)

Mistakenly labeled as "inert gases" until about 30 years ago because it was thought that
these gases did not react with anything.
In 1962, Neil Barlett isolated the first compound containing a noble gas: [Xe+][PtF6-]
2. Since then, compounds containing Kr, Xe, and Rn have been isolated, but none
containing He, Ne, or Ar.
3. The oxidation numbers of the rare gases in compounds include +1, +2, +4, +6, and +8.
4. Noble gases have filled valence (outermost) shells.
Electron Configuration
Example : 16S = 1s2 2s2 2p6 3s2 3p4

S2- = 1s2 2s2 2p6 3s2 3p6

Na+= 1s2 2s2 2p6

11

How to Determine Group and Period based on Electron Configuration


Example : 16S = 1s2 2s2 2p6 3s2 3p4

Group: the latest number electron in sub shell (VI A)


Periode: the latest number of shell (3)

Periodic Properties:
1. Atomic Radius : amount that when to be summed it will give inter nucleus distace among the
relevance atom
2. Electron Affinity: the energy where atom in the gaseous state is release when it captures an
electron so that became ion -1 charge unit.
3. Ionization energi: the minimum energy where atom in the gaseous state is to release electron.
4. Electronegativity: the ability of an atom to attract electron toward itself in a chemical bond.

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