The Structure
of the IPS 8th Edition Course
Link
to 7th edition structure
IPS has always had a central theme and a
clear story line not confined to a single discipline. The central them
is the study of matter leading to the development of the atomic model.
In broad terms, the course divides naturally into two parts. Chapters
1–6 provide the empirical framework without which the
atomic model becomes an answer in search of a question. The progression
is from what is around us in the greatest abundance, namely mixtures,
to compounds and elements. In the process, students learn about the characteristic
properties by which substances are recognized and separated. Chapters
7–10 use the discreteness of radioactive processes to
motivate the development of the atomic model. The atomic model is shown
to bring order to known facts and to allow us to make testable predictions.
Simple methods are used to determine the size and masses of molecules
and atoms. The periodic table is examined through a historical perspective
and serves as a culmination of the course. The division of the course along these lines provides natural breaking
points for teachers who wish to spread the IPS course
over more than one year or to integrate IPS with Force,
Motion, and Energy.
The
Story Line of the Eighth Edition of IPS
The following annotated table of
contents best describes the Eighth Edition story line: CHAPTER
1— VOLUME
AND MASS 1.1 Experiment: Heating Baking Soda
1.2 Volume
1.3 Reading Scales
1.4 Experiment: Measuring Volume by Displacement of Water
1.5 Mass: The
Equal-Arm Balance
1.6 Unequal-Arm Balances
1.7 Electronic Balances
1.8 Experiment: The Sensitivity of a Balance
As you introduce a new class to IPS,
try to set the tone for the entire year on the first day. The short
note “To the Student” (on
page x in the text) and Experiment 1.1, Heating Baking Soda, will help
you do this.
The purpose of the note is to alert students to the interplay of the
three forms of active learning in the course: experimenting, reading,
and solving problems. You may wish to read the note in class either before
or after Experiment 1.1.
Raising the question of how to compare amounts of solids, liquids,
and gases at the end of Experiment 1.1 serves as a motivation for the
study of volume and mass. We begin with volume, showing different methods
of measuring it and the need to say precisely what we mean by the volume
of an object. After pointing out the shortcomings of volume as a measure
of the quantity of matter, we then proceed to mass, which is operationally
defined as that property of matter that is measured with an equal-arm
balance. However, in practice, the course no longer requires the use
of the equal-arm balance.
Experiment 1.8, in which students determine the sensitivity of a balance,
has been written so that it can be done with equal-arm balances, unequal-arm
balances, or electronic balances.
CHAPTER
2 — MASS CHANGES IN CLOSED SYSTEMS 2.1 Experiment: The Mass of Dissolved Salt
2.2 Histograms
2.3 Using a Computer to Draw Histograms
2.4 Experiment: The Mass of Ice
and Water
2.5 Experiment: The Mass of Copper and Sulfur
2.6 Experiment: The Mass
of a Gas
2.7 The Conservation of Mass
2.8 Laws of Nature
Although this chapter is among the shorter ones in the text, it is
of prime importance. Interwoven in it are two objectives: the development
of the skills related to the balance and the analysis of data, and the
accumulation of evidence leading to a fundamental law of nature, the
law of conservation of mass. It will take the entire chapter to reach
the objectives.
Histograms,
which are introduced in this chapter, are used throughout the course.
The time you invest in teaching students how to construct them will
pay handsome dividends later on. Once students know how to construct
histograms by hand, we recommend that they use the KaleidaGraph software
to save time and explore various choices available to them.
Emphasize
to students that a single experiment, involving only one kind of change
(such as dissolving salt), is not in itself very convincing evidence
for concluding that mass does not change when other changes take place.
This is why four separate mass-conservation experiments, all involving
different kinds of change, are included in this chapter. Do not skip
any of them; let your students do all of them to convince themselves
of the plausibility of conservation of mass.
CHAPTER
3 — CHARACTERISTIC PROPERTIES
3.1
Properties of Substances and Properties of Objects
3.2
Experiment: Mass and Volume
3.3
Density
3.4
Dividing and Multiplying Measured Numbers
3.5
Experiment: The Density of Solids
3.6
Experiment: The Density of Liquids
3.7
Experiment: The Density of a Gas
3.8
The Range of Densities
3.9
Experiment: Freezing and Melting
3.10
Graphing
3.11
Experiment: Boiling Point
3.12
Boiling Point and Air Pressure
3.13
Identifying Substances
In daily
language one hears statements like “lead is heavier
than iron.” Of course, lead is neither heavier nor lighter than
iron, just as lead is neither bigger nor smaller than iron. Mass, volume,
and shape are properties of objects. Properties that do not depend on
the amount of a substance are called characteristic properties.
The characteristic
properties discussed in this chapter and in Chapter 4 have been selected
for their usefulness in identifying substances and separating mixtures.
Hence, we concentrate on density, freezing point, and boiling point
in this chapter, and on solubility in Chapter 4.
CHAPTER
4 — SOLUBILITY 4.1 Experiment:
Dissolving a Solid in Water
4.2
Concentration
4.3
Experiment: Comparing the Concentrations of
Saturated Solutions
4.4
Experiment: The Effect of Temperature on Solubility
4.5
Wood Alcohol and Grain Alcohol
4.6
Experiment: Isopropanol as a Solvent
4.7
Experiment: The Solubility of Carbon Dioxide
4.8
The Solubility of Gases
4.9
Acid Rain
4.10
Drinking Water
Solubility
is a characteristic property of both the solute and the solvent. It
is expressed in a complex unit—grams of solute per
100 cm 3 of solvent. If we know the solubility of a substance in a given
solvent and the quantity we want to dissolve, we can calculate the minimum
amount of solvent necessary. Or, if we know how much solvent we have,
we can use the solubility to find the maximum amount of the solute that
will dissolve in it.
Like density, solubility changes with temperature. However, the solubility
of some substances changes rather dramatically with temperature, whereas
the density of solids or liquids changes only slightly. The dependence
of solubility on temperature is very useful in separating substances
in solution.
CHAPTER
5 — THE SEPARATION OF MIXTURES 5.1 Experiment:
Fractional Distillation
5.2
Petroleum
5.3
The Separation of Insoluble Solids
5.4
Experiment: The Separation of a Mixture of Solids
5.5
The Separation of a Mixture of Soluble Solids
5.6
Experiment: Paper Chromatography
5.7
A Mixture of Gases: Nitrogen and Oxygen
5.8
Mixtures and Pure Substances
As we mentioned
earlier, one of the criteria for selecting characteristic properties
for discussion is their usefulness in separating substances. Now we
will employ these properties for actual separations in the laboratory,
describe some applications of these methods in industry, and arrive at
an operational definition of a pure substance.
Reading
through this chapter, you may get the impression that we are leaving
students with a rather vague definition of a pure substance. This is
true. The boundary between a mixture and a pure substance is not so
sharp as may be believed from reading some textbooks. If your students
realize at the end of this chapter that a pure substance is something
that cannot be broken up by any of the methods discussed, they will
have learned their lesson.
CHAPTER 6 — COMPOUNDS AND ELEMENTS 6.1 Breaking
Down Pure Substances
6.2
Experiment: The Decomposition of Water
6.3
The Synthesis of Water
6.4
Experiment: The Synthesis of Zinc Chloride
6.5
The Law of Constant Proportions
6.6
Experiment: A Reaction with Copper
6.7
Experiment: The Separation of a Mixture of Copper
Oxide and Copper 6.8
Complete and Incomplete Reactions
6.9
Experiment: Precipitating Copper
6.10
Elements
6.11
Elements Near the Surface of the Earth
By definition,
pure substances are not broken up into different components by those
separation methods used to separate mixtures. The aim of this chapter
is to show that, in general, pure substances can, nevertheless, be
broken up by other means, such as applying intense heat or an electric
current. Conversely, such pure substances (compounds) can also be synthesized
from other pure substances, but only by reacting in definite proportions.
After recalling
the decomposition of two pure substances by heating, we use electrolysis
to break up water (Experiment 6.2). New pure substances are produced
that are quite different from the original substance. We then reverse
our method of attack and synthesize compounds. The examples used are
chosen to illustrate one of the basic differences between compounds
and mixtures: unlike mixtures, compounds can be synthesized only by
reacting the components in definite proportions (Sections 6.3 – 6.5).
Early difficulties
in the formation of the law of constant proportions sprang in part
from the difficulty of determining when a reaction was complete. The
reaction between copper and oxygen (Experiments 6.6 and 6.7) illustrates
this circumstance: The investigation into what has happened leads to
an understanding of complete and incomplete reactions.
Experiment
6.9 ends the sequence of experiments that started with Experiment 6.6
and continued in Experiment 6.7. Copper was used to form a series of
pure substances and was then recovered, suggesting that the copper
was there all along. The section leads into the operational definition
of elements (Section 6.10). The reasoning used in the definition of an
element is reinforced with two historical examples. Be sure to spend
enough time on this section.
Section
6.11 balances the preceding discussion of scientific methodology with
a discussion of the abundance of elements near the surface of the earth.
CHAPTER
7 — RADIOACTIVITY 7.1 Radioactive
Elements
7.2
Radioactive Decomposition
7.3
Experiment: Radioactive Background
7.4
Experiment: Collecting Radioactive Material on a Filter
7.5
Experiment: Absorption and Decay
7.6
A Closer Look at Radioactivity
7.7
Radioactivity and Health
You may
wonder why we proceed with the introduction of radioactivity at
this point in the course. Here are the reasons:
(i) It provides an excellent example of the surprises that nature has
in store for us: Now that students have learned how elements survive
in the formation of compounds, they find that some elements actually
change into other elements all on their own.
(ii) This change takes place in discrete steps, which can be counted.
(iii) Taken together, (i) and (ii) provide a motivation for the atomic
model of matter and lead to a testable prediction (Chapter 8).
(iv) Being able to count radioactive decays enables us to find the
number of atoms in a given sample of an element. This, in turn, provides
a conceptually simple way to find the mass of single atoms solely with
the knowledge students gained in this course (Chapter 9).
(v) Knowing the mass of atoms enables us to introduce the periodic
table in a meaningful way (Chapter10).
In addition,
it should be noted that radioactivity is largely ignored in the science
curriculum. For many students, learning about radioactivity in IPS may
be the only chance to do so.
Randomness,
discreteness, and absorption can be demonstrated quite easily in
the classroom. However, demonstrating decay and the existence of
a half-life requires a source with a short half-life. The only practical
way to get such a source is to collect it yourself. You will be able
to do this if there is a sufficient concentration of radon in the
ground around your school, and if your school has a closed, unventilated
room in the basement in which radioactive material can be collected
from the air.
Unlike
in other chapters, the three experiments in Chapter 7 are to be done
by the class as a whole rather than by pairs of students. The reason
is simple: it is unlikely that you will have enough Geiger counters.
However, if you have more than one counter, divide the class into
smaller groups and have them work in parallel. The class will have
the advantage of seeing that while the details vary, the general
trend is the same.
CHAPTER
8 — THE ATOMIC MODEL OF MATTER 8.1 A Model
8.2
Experiment: A Black Box
8.3
The Atomic Model of Matter
8.4 “Experiment”:
Constant Composition Using Fasteners and Rings
8.5
Molecules
8.6
Experiment: Flame Tests of Some Elements
8.7
Experiment: Spectra of Some Elements
8.8
Spectral Analysis
8.9 “Experiment”:
An Analog for Radioactive Decay
8.10
Half-Life
We now
introduce the atomic model of matter, which will continue to be at
the center of our attention through Chapter 10.
After a
brief introduction to the meaning of a “model,” the
class applies the idea to a “black box,” which provides an
opportunity to make testable predictions (Experiment 8.2).
Sections
8.3–8.5 sum up key observations made
earlier in the course in the context of the atomic model. The law of
conservation of mass and the law of constant proportions are given
special attention.
In Sections 8.6 and 8.7, the class experiments with spectra of atoms
and is shown evidence that the spectra display properties of the individual
atoms rather than properties of the elements in bulk.
Finally, the atomic model is used to predict the existence of a half-life
for radioactive elements.
CHAPTER
9 — THE SIZES AND MASSES OF MOLECULES
AND ATOMS 9.1 The
Thickness of a Thin Layer
9.2
Experiment: The Thickness of a Thin Sheet of Metal
9.3
Experiment: The Size and Mass of an Oleic Acid Molecule
9.4
The Mass of Helium Atoms
9.5
The Mass of Polonium Atoms
9.6
Atomic Masses and Molecular Formulas
One of
the key ingredients of the atomic model introduced in Chapter 8 was
that atoms are very light and small, or, equivalently, that there are
many atoms in any sample of an element of measurable mass. Building
the atomic model on this premise demands an answer to the question, “What
is the mass of a single atom of an element?” In this chapter we
answer the question.
We arrive
at our goal in stages, by preparing the students for the main sections
(Sections 9.4 and 9.5). We first find the thickness of an aluminum
foil. We then apply the same approach to find the thickness of a layer
of oleic acid (Sections 9.1–9.3).
Sections
9.4 and 9.5 parallel the film, “The Mass of Atoms,” which
is now available in VHS and DVD formats, and adds a lively dimension
to the presentation in the text. Finally, the knowledge of atomic masses
is applied to finding molecular formulas (Section 9.6).
CHAPTER
10 — THE CLASSIFICATION OF ELEMENTS:
THE PERIODIC TABLE 10.1 Introduction
10.2
Classifying Elements
10.3
The Extraction of Similar Elements from Similar Compounds
10.4
Alkali Metals, Alkaline Earth Metals, and Halogens
10.5
Activity: Atomic Mass and Other Properties of Atoms
10.6
The Elements in the Third Through Sixth Columns
10.7
Activity: Elements in the Fourth Row
10.8
The Fourth and Fifth Rows: An Historical Perspective
Chapter
10, which is new to the Eighth Edition, provides a climax to the year’s
work by tying together many observations on the macroscopic and atomic
levels. We begin by asking if there is any relationship between atomic
mass and various properties of the elements (Section 10.1). This leads
us to the question of how to classify elements (Sections 10.2–10.4).
Some of the historical comments extend similar comments in Chapter 6.
To drive home the point that any classification is a matter of judgment,
we have the students do an activity with a set of 24 specially prepared
cards (Section 10.5). The cards resemble entries in a periodic table
of the elements. The activity has historical connotations, and raises
the question of the order of potassium and argon. The activity is briefly
extended in Section 10.7 to show the need for additional columns in the
periodic table.
The chapter
ends with an analysis of the periodic table as a model, and shows its
success by highlighting Mendeleev’s
correct prediction of the properties of germanium before the element
was discovered.
APPENDIX: Calculating in Scientific Notation Part 1
Scientific Notation
Part
2 Multiplying and Dividing in Scientific Notation:
Significant
Digits
The appendix provides instruction and practice for students who need
to improve their skill calculating with numbers in scientific notation.
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