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8/3/2019 Basic Chemistry I (Print)
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Basic Chemistry I
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MATTER AND ENERGY
Matter
All the materials that interest
chemistsin fact, all the things we
can see or touch or feelare
examples ofmatter, whether they bebooks, pencils, telephones,
hamburgers, or people.
Matter is defined as anything that
takes up space and has mass. In
setting down this definition, we are
very careful to specify the term mass
rather than weight, even though we
often use the terms as if they were
interchangeable. Mass and weight
are not really the same.
A Ping-Pong ball moving at 30 km h -
1 (30 kilometers per hour), for
example, is easily deflected by a softbreeze, but a cement truck moving at
the same speed is not.
Quite clearly, the mass of the cement
truck is considerably greater than
that of the Ping-Pong ball.
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The term weight refers to the force
with which an object of a certain
mass is attracted by gravity to the
earth or to some other body that it
may be near, such as the moon.
Force and mass are related to each
other by Newton's equation
(Newton's law).
F = ma
whereF= force, m = mass, and
a = acceleration. In order to accelerate a
body, a force must be applied to it. When an
object is dropped, it accelerates because of
the gravitational attraction of the earth. An
object resting on the earth or moon exerts a
force (its weight, W) that is equal to its
mass, m, multiplied by the acceleration due
to gravity,g, that is,
W= mg
For example, at the earth's surface,g
= 9.81 m s-2.
Thus a one-kilogram mass would
have a weight (or experience a force
downward at the earth's surface) of
For convenience, the derived SI unit
of force or weight, possessing units 1
kg m s
-2
, is defined as the newton(N).
A one-kilogram mass has a we 9.81
N at the earth's surface. You can
experience the magnitude of a one
force by placing a large lemon (or
any object with slightly more than
100 g mass in your hand; the "push"
downward represents a one-newton
force..' moon the gravitational
acceleration is only about one-sixth
of that on earth, so the same object
weighs only one-sixth as much on
the moon as on the earth, even
though its mass is the same in both
locations.
Even on the earth the value ofghas
been found to vary slightly from
place to place. This means that if
very precise measurements are made,
an object's weight also varies slightly
according to its location on the earth.
Because of this, we specify an
object's mass instead of its weight
when we wish to report the quantity
of matter in the object.
The measurement of mass (a process,
oddly enough, called weighing) is
actually performed by comparing the
weights of two objects, one of
known mass, the other of unknown
mass.
The apparatus used for this is called
a balance. Figure 1.7 is a drawing of
a traditional two-pan balance. The
object to be weighed is placed on the
left pan of the balance and objects of
known mass are added to the other
until the pointer comes to the center
of the scale.
At this point the contents of both
pans weigh the same, and since they
both experience the same
gravitational acceleration, both pans
contain equal masses.
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In chemistry, as mentioned
previously, we generally measure
mass in grams.
Most balances found in labs today
function on the same principle. Themost modern electronic balances,
operate on a somewhat different
principle. They are rugged, fast, and
convenient, and make the
measurement of mass a routine
laboratory operation.
Energy
When chemical changes occur, theyare almost always accompanied by
either an absorption or release of
energy.
These energy changes tell us a great
deal about the nature of the
chemicals that are reacting, and
equally important to us, certain
chemical reactions provide the
energy that our bodies and oursociety need in order to function.
Therefore, an understanding of what
energy is and how it can be
transferred from one object to
another is as important to those who
study chemistry as an understanding
of matter itself.
Energy itself is a difficult concept tocomprehend, because energy is so
different from matter. You can't put
energy in a bottle to examine it. All
you can do is examine the effects of
energy on objects.
Energy is usually defined as the
capacity to do work or to make
things happen. When an object has
energy, it can affect other objects by
doing work on them.
A moving car possesses energy
because it can do work on another
car by moving it some distance in a
collision.
Coal and oil possess energy because
they can be burned and the heat that
is liberated can be harnessed to do
work.
Because energy can be transferred
from one object to another as work,
the units of energy and work are the
same.
An object can possess energy in two
ways: as kinetic energy and as
potential energy. Kinetic energy
(K.E.) is associated with motion and
is equal to one-half of an object'smass, m, multiplied by its velocity,
v, squared.
Thus, we see that the amount of
work a moving body can do depends
on both its mass and its velocity.
For example, a truck moving at 30 km h-1
can do more work on the rear end of a car
than a bicycle moving at the same speed.We also know that a truck moving at 80 km
h-1 can do more work on a car than one
traveling at only 5 km h-1.
Potential energy (P.E.) represents
energy a body possesses because of
the attractive or repulsive forces it
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experiences with other objects. If
there are no attractive or repulsive
forces, the body does not possess
potential energy.
As we have indicated, chemicalsubstances contain energy that can
be released through chemical
reactions. For example, when wood
burns, it reacts with oxygen from the
air. As the products of combustion
are formed, rather sizable quantities
of heat are released. In this case, the
wood and the oxygen are sources of
potential energy, sometimes called
"chemical energy," and the reaction
causes this energy to be released into
the surroundings as heat.
The quantity of energy released or
absorbed in a chemical reaction
depends on the amounts of materials
that react.
The burning of a match, for example,
releases only a very small quantity of
energy, but a large bonfire produces
much more.
When a change (either chemical or
physical) releases energy to the
surroundings, it is called an
exothermic change. Changes that
absorb energy are termed
endothermic.
It is usually easy to recognize
whether a process is exothermic or
endothermic; an exothermic change
raises the temperature of its
surroundings, and an endothermic
change causes its surroundings to
become cool
The total quantity of energy that an object
possesses is equal to the sum of its kinetic
energy and its potential energy. In anisolated system, such as we believe our
universe to be, the total quantity of energy is
constant. This leads to a very important
physical law, called the law of conservation
of energy, which states that energy can be
neither created nor destroyed. It only can be
changed from one kind of energy to another.
Units of energy
Energy is transmitted from one body
to another in a variety of ways, for
example, as light, sound, electricity,
and/or heat. These various forms of
energy can be converted from one to
another and therefore are ultimately
equivalent.
The SI (System International) unit
for energy is the joule (J), which isdefined as 1 kg m2/s2 in terms of the
SI base units. It represents the kinetic
energy possessed by an object with a
mass of 2.0 kg traveling at 1 m/s.
In referring to energies involved in
chemical reactions, it is useful to use
the term kilo joule (kj). One kilo
joule is equal to 1000 joules (1 kj =
1000 J).
All forms of energy ultimately are
transformed into heat, and when
chemists measure energy, it is
usually in the form of heat.
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We know that heat always flows by
itself from a region of high
temperature to one of low
temperature, as when a hot cup of
coffee becomes cool.
We also know that the rate of heat
transfer depends on the difference in
temperature between two objects. If
we want to warm something slowly,
we place it in contact with an object
just slightly warmer; if we wish to
heat it quickly, we place it in contact
with something very hot.
The original definition of the unit of
heat energy called the calorie
(symbolized cal) relied on the
concept of temperature. The calorie
was defined as the quantity of heat
needed to raise the temperature of 1
gram of water, initially at 15C, by
1C.
The kilocalorie (kcal), like the
kilojoule, is a more appropriately
sized unit for dealing with energy
changes in chemical reactions.
For example, we might measure the
heat liberated during the combustion
of natural gas, which is composed
principally of the compound
methane. The measurement of heat
involves the concept of temperature,
which we discussed earlier.
It is important to remember that heat
is not the same as temperature. Heat
is energy, while temperature is a
measure of the intensity of heat or
hotness. Another useful definition of
temperature is that it defines the
direction and rate of heat flow.
It has also been the unit used in
nutrition for reporting the energy
content of foodsthe Calorie(written with a capital C) is the same
as a kilocalorie. Thus, if we read that
a serving of mashed potatoes
contains 230 Cal, we are being told
that 230 kcal of energy are liberated
when the body metabolizes this food.
Until recently, nearly all the
chemical scientific literature used the
calorie (or kilocalorie) in reportingenergy changes. With the
introduction of SI units, the joule (or
kilojoule) is now preferred and the
calorie has been redefined in terms
of this SI unit. The calorie and
kilocalorie are defined exactly by the
relationships
1 cal = 4.184 J
1 kcal = 4.184 kJ
Thus in terms of SI, one Calorie of
food energy is more properly
expressed as 4.184 kJ.
PROPERTIES OF MATTER
Objects are recognized by their
characteristics, or properties. For
example, Iron has shiny surfaces,
pull by magnet, react with oxygen
produce rust. If we burn magnesium,
bluish white color is emitted. Boiling
point of alcohol is lower than water.
Luster, color, magnetism, the
tendency to corrode, boiling point
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are just some of the many properties
that we use to recognize and classify
different samples of matter.
These properties themselves can be
divided into two broad categories:extensive properties, which depend
on the size of a sample of matter; and
intensive properties, which are
independent of the sample size. Of
the two, intensive properties are the
more useful, because a substance
will exhibit the same intensive
property regardless of how much of
it we examine.
Examples of extensive properties are
mass and volumeas the amount of
a substance increases, its mass and
volume also increase. Some
examples of intensive properties are
melting point and boiling point.
Another intensive property is
density, which is defined as the ratio
of an object's mass to its volume.
Liquid water, for instance, has a
density of 1 g/ cm3. This means that
if we had 1 g of water, it would
occupy a volume of 1 cm3. If we had
20 g of water, it would occupy a
volume of 20 cm3, but the ratio of
the water's mass to its volume is the
same: 20 g/20 cm3 = 1 g/1 cm3 = 1 g
cm-3. Notice that we have created an
intensive property by taking the ratio
of two extensive ones. Later in our
discussion of chemistry, we will
encounter quite a few other intensive
properties defined in a similar way.
Normally, when a substance is
heated or cooled, its volume expands
or contracts. This means that the
object's mass is packed into either a
larger or smaller volume, so the
density also changes with
temperature.
Therefore, for very accurate work,
the temperature corresponding to a
reported density must be specified.
For example, at 25.0C (room
temperature) the density of water is
0.9970 g cm-3, while at 35.0C its
density is 0.9956 g cm-3. (For most
purposes, we can take the density of
water to be 1.00 g cm-3.)
Density provides a relationship
between an object's mass and its
volume. It tells us, in this instance,
that if we have 1.00 cm3 of copper,
its mass is 8.96 g. It also tells us that
if we have 8.96 g of copper, its
volume is 1.00 cm3. We call/use the
density as a conversion factor in two
ways
Since we are given the mass of
copper, we must multiply by the
second factor to eliminate the units
grams.
A property closely related to density
is specific gravity (often abbreviated
sp.gr.), or relative density, which is
defined as the ratio of the density of
a substance to the density of water.
In this way two tablesone
containing the specific gravities of
substances and the other containing
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the density of water in a variety of
unitstake the place of the many
tables that would otherwise be
needed to express the densities of
substances in all those different
units.
EXAMPLE 1.9 PROBLEM
FINDING SPECIFIC GRAVITY
Hexane, a solvent used for rubber
cement, has a specific gravity of
0.668. What is the density of hexane
in g cm-3 and in kg m-3. Water has a
density of 1.00 g cm-3 or 1.00 x 103
kg m-3.
SOLUTION
By definition:
dhexansp. gr. hexane = ------------
dwater
Therefore
(sp. gr. hexane) x dwater= dhexan
In units of grams per cubic centimetre
dhexan = (0.668) x (1.00 g/cm3) = 0.668 g
cm-3
Notice that in units of g cm -3 the
numerical values of density and
specific gravity are the same.
In units of kilograms per cubic
metre,
dhexan =
(0.668) x (1.00 x 103 kg/m3) = 6.68 x 103
kg m3
Specific heat capacity
An intensive property of matter associatedwith energy is specific heat capacity
(sometimes termed specific heat), the
quantity of heat required to raise the
temperature of 1 g of a substance by 1C.
The specific heat capacity of water is 4.184
J g-1C-1. Most other substances have
smaller specific heats. Iron, for example, has
a specific heat of only 0.452 J g-1oC-1. This
means that it takes less heat to raise thetemperature of 1 g of iron by 1C than it
does to cause the same temperature change
for a gram of water. It also means that a
given quantity of heat will raise the
temperature of 1 g of iron more than it will
raise the temperature of 1 g of water.
The large specific heat capacity of
water is responsible for the
moderating effect the oceans have onweather, since they cool very slowly
in winter and warm up slowly in the
summer.
Air moving over the oceans in winter
never gets very cold, and in the
summer the air never gets very hot.
EXAMPLE 1.10 CALCULATIONS
INVOLVING SPECIFIC HEAT
PROBLEM
How many joules are required to raise the
temperature of a 7.5-cm iron nail with a
mass of 7.05 g from room temperature
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(25C) to 100C? The specific heat capacity
of iron is 0.452 J g-1 oC-1.
SOLUTION
To solve this problem, we must multiplythe specific heat capacity by mass (g) and
the temperature change (C) to eliminate
these units and obtain joules as the units of
the answer.
specific heat capacity x mass x
temperature change = heat energy
Notice that the answer has been rounded to
two significant figures. Do you know why?
If not, review the significant figure rules for
multiplication.
Physical and chemical properties
In speaking of the properties of
substances, we also distinguish
between physical properties and
chemical properties. A physical
property can be specified without
reference to any other substance.Density, specific heat, color,
magnetism, mass, and volume are all
examples of physical properties.
A chemical property, on the other
hand, states some interaction
between chemical substances. When
iron is exposed to oxygen and water,
it corrodes and produces a new
substance called iron oxide rust.
This is a chemical property of iron.
We also say, for instance, that
sodium is very reactive toward
water. Reactivity is a chemical
property that refers to the tendency
of a substance to undergo a particular
chemical reaction.
However, to say simply that a
substance is very reactive, without
specifying "with what" or underwhat conditions, is not particularly
helpful. Sodium, for example, is very
reactive with water but quite
unreactive toward the gas helium.
ELEMENTS, COMPOUNDS, AND
MIXTURES
In nature, there are very few material
that even approach being pure compoundsnearly everything is a mixture.
The three words that form the title to this
section lie very close to the heart of
chemistry, because we work with elements,
compounds, and mixtures in the laboratory.
We must therefore understand what they are
and how to distinguish among them.
Elements are the simplest forms of
matter that can exist underconditions that we find in a chemical
laboratory; they thus are the simplest
forms of matter with which the
chemist deals directly. Elements
serve as the building blocks for all of
the more complex substances that we
encounter, from common table salt to
extremely complex proteins.
All are composed of a limited set ofelements. At present, there are 108
known elements, but only a much
smaller number will be of real
interest to us.
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Elements combine with each other to
form compounds. A compound is
characterized by having its
constituent elements always present
in the same proportions. For
example, you probably know that
water is composed of two elements:
hydrogen and oxygen. All samples of
pure water contain these two
elements combined in the proportion
of one part by mass hydrogen to
eight parts by mass oxygen (for
example, 1.0 g of hydrogen to 8.0 g
of oxygen). Also, when hydrogen is
allowed to react with oxygen toproduce water, the relative quantities
of hydrogen and oxygen that
combine are always the same.
Thus, whenever 1.0 g of hydrogen
reacts, it is always observed that only
8.0 g of oxygen are consumed, even
if more than that quantity of oxygen
is available.
Mixtures differ from elements and
compounds in that they may be of
variable composition. (As a result,
they are not considered to be pure
substances.) A solution of sodium
chloride (table salt) in water is a
mixture of two substances. We know
that by dissolving varying quantities
of salt in water (or a bowl of soup),
we can obtain solutions with a widerange of compositions. Most materi-
als found in nature or prepared in the
laboratory are not pure but instead
are mixtures.
Mixtures can be described as being
either homogeneous or
heterogeneous. A homogeneous
mixture is called a solution and has
uniform properties throughout. If we
were to sample any portion of a
sodium chloride solution, we would
find that it has the same properties
(e.g., composition) as any other
portion of the solution; we say that it
consists of a single phase. Thus, we
define a phase as any part of a
system that has uniform properties
and composition.
A heterogeneous mixture, such as oil
and water, is not uniform (Figure
1.11). If we were to sample one
portion of the mixture, it would have
the properties of water, while some
other part of the mixture would have
the properties of oil. This mixture
consists of two phases: the oil and
the water.
If we shook the mixture so that the
oil was dispersed throughout the
water as small droplets (as in a salad
dressing), all the oil droplets taken
together would still constitute only a
single phase, since the oil in one
droplet has the same properties as the
oil in another. If we added an icecube to this "brew," we would then
have three phases: the ice (a solid),
the water (a liquid), and the oil
(another liquid). In all these
examples, we can detect the presence
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of two or more phases because a
boundary exists between them.
A useful feature of pure substances is
that they undergo phase changes
(e.g., solid to liquid or liquid to gas)at constant temperature. Ice, for
instance, melts at a temperature of
0C, a temperature that remains
constant while the water undergoes
the change from solid to liquid.
When mixtures undergo phase
changes, they generally do so over a
range of temperatures. This
phenomenon provides us with oneexperimental test to determine when
we have obtained a pure substance.
There is another way that mixtures
differ from compounds and
elements. When a mixture is
prepared, the chemical properties
(and often, the physical properties)
of the components do not change,
but when elements are combined to
form a compound, very profound
changes occur in both chemical and
physical properties. For example,
copper and sulfur are two elements.
Copper, of course, is a reddish-
colored metal, a good conductor of
electricity, and is relatively resistant
to corrosion. Sulfur is a yellow
nonmetallic substance
A mixture of sulfur and copper is
easily prepared, but in the mixture
we can still see traces of the
properties of copper and the
properties of sulfur. The formation of
the mixture has involved a physical
processa process that has not
altered the chemical characteristics
of the components.
If the mixture of copper (Cu) and
sulfur (S) is heated, a chemicalreaction, or chemical change, takes
place. The copper and sulfur
combine to form a compound and
this is accompanied by dramatic
changes in the properties of the
substances. After the reaction is
over, we can't find anything that has
the properties copper, and we can't
find anything that has the properties
of sulfur. We find a new substance,
called copper(II) sulfide, that has
new properties.
Figure 1.12
(a)Alongside a crucible and its
cover we see a coil of red-colored
copper wire and yellow powdered
sulfur, (b) When mixed in the
crucible, the copper and sulfurretain their individual properties, (c)
When the mixture of copper and
sulfur is heated, a reaction takes
place and a new substance called
copper(ll) sulfide is formed. The
copper(ll) sulfide has the same
shape as the coiled copper wire from
which it was formed. Notice that its
properties differ from both the
copper and sulfur.
It doesn't conduct electricity; it
doesn't have the color of either
copper or sulfur; it has a density that
is different from both sulfur and
copper; and its chemical properties
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are entirely different, too. Such
changes are what characterize
chemical reactions.
Separating elements, compounds, and
mixtures
Since elements form compounds by
chemical reactions, decomposing
compounds into their elements also involves
chemical reactions, and they also are
accompanied by drastic changes in
properties.
Mixtures can be separated by physical
processes in which the chemical propertiesof the components are not altered. Even so,
separating mixtures is not always an easy
job, and a variety of methods have been
devised by chemists for this purpose.
For example, a mixture of salt in water can
be left to evaporate, and the departure of the
water leaves the salt behind as a solid
If we wished to recover the water as
well, we could boil the mixture in an
apparatus similar to the one in Figure
1.14 and collect the water after it has
condensed from the steam. This
process is called distillation. It is one
method that is used to obtain
drinking water from sea water (the
desalination of sea water).
Another method of separating
mixtures, called chromatography,
makes use of the different tendencies
that substances have for being
adsorbed onto the surface of certain
solids. For example, in thin-layer
chromatography (Figure 1.15), a
small spot of a solution containing
several components is placed onto
one end of a glass plate that is thinly
coated with a material such as silica
gel.
A suitable solvent is then allowed tocreep up the coating from a
reservoir. As the solvent flows past
the spot, the different components
tend to be lifted from the silica gel
surface with different degrees of
ease.
This causes the components of the
mixture to move through the silica
gel at different rates, with the morestrongly adsorbed components
moving more slowly.
The result is a separation of the
original spot into a set of spots, each
containing (we hope) one compo-
nent. This technique is widely used
today by chemists who synthesize
new compounds.
Ilustrasion of separating process
Plogiston theory
The early history of chemistry was marked,
not surprisingly, by incorrect theory about
what occurred during chemical reactions. It
had long been observed for example, that
when the combustion of wood took place,
was very light and fluffy. Metals alsochanged their appearance when heated in
air. The resulting material was less dense
than the original metal and thus appeared
lighter.
These observations led to the conclusion
something which the German chemists
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philosophers Leucippus and Democritus
suggested, as early as 400 to 500 b.c., that
matter cannot be forever divided into
smaller and smaller parts and that ultimately
particles would be encountered that would
be indivisible. These early proposals,
however, were not based on the results of
experiments and were little more than
exercises in thought.
Dalton's theory was different because it was
based on the laws of conservation of mass
and definite proportions, laws that had been
derived from many direct observations.
The theory Dalton proposed can beexpressed by the following
postulates:
1. Matter is composed of indivisible
particles called atoms.
2. All atoms of a given element have the
same properties (e.g., size, shape, and mass),
which differ from the properties of all other
elements.
3. A chemical reaction merely consists of a
reshuffling of atoms from one set of
combinations to another. The individual
atoms themselves, however, remain intact.
SOME PROPERTIES OF THE
ELEMENTS
The range of properties shown by the
elements is tremendous. At roomtemperature, some are gases, two are
liquids, and the rest are solids.
Some are metallic and some are not,
and some have properties in
between. Some are hard and some
are soft; some are very dense and
others have very low densities. With
such variety, we have to look for
ways to classify these properties so
that it is possible to make some sense
out of them.
One of the simplest methods of
classification is to divide the
elements into three categories:
metals, nonmetals, and metalloids.
The elements in each of these
categories have certain distinctive
characteristics.
Metals
Everyone has seen metals of one
kind or anotheran iron nail,
aluminum foil, copper wire, or a
"chrome-plated" bumper on a car, for
example. And you are no doubt
familiar with some of the properties
that characterize metals, even if you
haven't thought about them very
much. One of these, for instance, is
the distinctive appearance that metals
have.
They shine with a luster that is so
characteristic that it's called a
metallic luster.
Metals are also similar in their
abilities to deform without breaking
when hit with a hammer and tostretch when pulled.
All metals have both these properties
to some degree. The ability to
deform when hammered is called
malleability, and some metals, such
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as gold, can be hammered or
squeezed into extremely thin sheets.
Gold leaf(Figure 3.1), for example,
consists of gold with a small amount
of silver and copper that has beenbeaten into sheets that are so thin
(about 90 nm) that they are
translucent; some light can actually
be seen passing through them.
Malleability is also a property that a
blacksmith relies on when forging a
horse-shoe, and a silversmith uses
the malleability of silver in
hammering a design into a fine silver
tray.
The ability of a metal to stretch when
pulled from opposite directions is
called ductility. This property is used
in the manufacture of wire, which is
illustrated in Figure 3.2. The metal to
be made into wire, which might be
steel, copper, or brass, is first formed
into a rod. One end is tapered, fed
through a
die, and attached to a pulling device
on the other side. The metal is then
drawn through the die where it
undergoes a reduction in size and an
increase in length.
Everyone knows that metals are
good conductors of electricity. They
are also good conductors of heat.
If you have ever touched a metal
object that has been lying in the sun
for a while, you know how very hot
it feels. In fact, it feels much hotter
than other objects alongside that are
not metallic. The reason is that as
your hand absorbs heat from the
metal, heat travels quickly from the
neighboring parts of the object to
replace it.
Nonmetallic objects don't feel as hotbecause when your hand removes
heat, it can't be replaced rapidly, and
the part of the object in contact with
your hand becomes cooler.
More than 70% of the elements are
metals, and although there are some
similarities among them, there are
many differences, too.
Some metals are quite common and
we encounter them nearly every day
in their elemental forms, that is,
uncombined with other elements.
The metals mentioned previously
(iron, aluminum, copper, and
chromium) are only a few examples.
There are other metals that are so
reactive only chemists, or chemistrystudents, ever have an opportunity to
see them. For example, in Chapter 1
we mentioned the reaction between
sodium and chlorine to form sodium
chloride, common table salt.
Sodium is a very reactive metal that
combines not only with chlorine, but
avidly with both oxygen and
moisture. In Figure 3.3, we see a barof sodium, heavily tarnished on the
outside, but the element's bright
metallic luster is revealed by the
freshly cut slice of the metal.
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The range of chemical reactivity of
metals is very broad. Sodium is
typical of one extreme, while gold is
typical of the other. Jewelry is made
from gold for several reasons, one of
which is the fact that it doesn't
tarnish when exposed to air and
moisture.
This very low reactivity, combined
with gold's high electrical
conductivity, accounts for one of this
metal's most important commercial
uses: the plating of electrical
contacts in computers and other
electronic devices.
Besides chemical reactivity, metals
differ in certain physical properties
such as hardness and melting point.
Some metals are very hard, and some
are very soft. Chromium and iron are
examples of hard metals; gold and
lead are examples of soft ones.
Sodium is also a soft metal; in Figure
3.3, we see it being cut with a knife.
The extremes of melting point are
even more impressive.
Tungsten has the highest melting
point of any element, 3400C, which
accounts for its use as the filament in
electric light bulbs.
Mercury has the lowest melting point
of any metal, -38.9C, which means
that it is a liquid at room
temperature. As you know, mercury
is the fluid commonly used in
thermometers.
Nonmetals
Most of the nonmetallic elements
(the nonmetals) are rarely
encountered in our daily activities in
their elemental forms; instead, they
are usually found in compounds.
One nonmetal that most people have
seen is carbon, which occurs in
nature in two different forms (Figure
3.4). The more common variety is
called graphite. This is the form that
we find in charcoal briquets and the
lead in lead pencils. The less
common and more valuable form of
carbon is diamond. Graphite and
diamond have properties that are
quite different from those that we
associate with metals. Neither has
the luster of a metal, and neither is
malleable or ductile.
Other nonmetals that you have
encountered are oxygen and
nitrogen, which are the principal
components of the atmosphere.
Usually, you are not aware of their
existence, because they are colorless
gases and you can't see them.
Oxygen and nitrogen occur as
diatomic molecules, molecules
containing two atoms each. Other
nonmetallic elements form similar
molecules, and most are gases, also.
These are hydrogen (H2), fluorine(F2), and chlorine (Cl2). Bromine
(Br2) and iodine (I2) are also
diatomic, but bromine is a liquid and
iodine is a solid at room temperature.
Just as the properties of the metals
cover a broad range, so do the
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properties of the nonmetals. As
we've seen, some are gases and one
(bromine) is a liquid. There are
others that are solids; carbon is just
one example. Besides differing in
these physical properties, nonmetals
differ from each other in their
chemical properties.
Fluorine, for example, is extremely
reactive while helium is inert(totally
unreactive). These differences,
which are very important, will be
explored in more detail later in the
book.
Metalloids
Metalloids are elements that have
properties that are intermediate
between those of metals and those of
nonmetals.
The best known example is the
element silicon. Two others are
arsenic (As) and antimony (Sb),which are shown in Figure 3.5. In
terms of outward appearances, these
elements have something of a
metallic look about them, but their
dark color gives them away. They
certainly differ in appearance from
typical metals such as iron or silver.
Metalloids are typically
semiconductorsthey conduct
electricity, but not nearly as well as
metals. These semiconductor
properties are especially valuable in
the electronics industry, because they
make possible all the microelectronic
devices found in hand-held
calculators and microcomputers.
Except for their electrical properties,
however, the metalloids are much
more like nonmetals than metals.
3.2 THE FIRST PERIODIC
TABLE
Chemical and physical properties
like those described in the last
section were discovered early on in
the history of chemistry.
Scientists, even as early as 1800, had
accumulated significant quantities of
information about the elements
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known to them. This knowledge,
however, existed for the most part as
isolated and unrelated facts that
needed to be correlated in some
fashion before their total significance
could be grasped.
Early attempts at a classification of
the elements met with only limited
success, and it wasn't until 1869 that
the forerunner of our modern
periodic table was devised. This
resulted from the work of two
chemists, a Russian named Dmitri
Mendeleev and a German named
Julius Lothar Meyer. Both worked
independently and produced similar
tables at about the same time.
Mendeleev presented the results of
his work to the Russian Chemical
Society in the early part of 1869, but
Meyer's table didn't appear until
December of that same year.
Because Mendeleev had the good
fortune of publishing first, he is
usually given credit for the periodic
table.
Mendeleev was a chemistry teacher,
and while he was preparing a
textbook for his students, he
discovered that if he arranged the
elements in order of increasing
atomic weight, elements with similar
properties occurred at periodic
intervals. For example, he could pick
out the elements lithium (Li), sodium
(Na), potassium (K), and rubidium
(Rb). Each of these elements forms a
water-soluble compound with
chlorine that has the general formula,
MCI, where M stands for Li, Na, K,
and so on. Although this is an
interesting fact by itself, what is
especially significant is that if we
examine the elements that
immediately follow Li, Na, K, and
Rb in the list, they form another
group of similar elements.
Thus, Be follows Li, Mg follows Na,
Ca follows K, and Sr follows Rb.
These elements form the compounds
BeCl2, MgCl2, CaCl2, and SrCl2.
Recognizing this, Mendeleev dividedthe list into a series of rows and
stacked them so that those elements
having similar properties are
arranged in vertical columns. The
result was the first periodic table,
which is illustrated in Figure 3.6