Title: A STUDY OF HOW PRECURSOR KEY CONCEPTS FOR ORGANIC CHEMISTRY SUCCESS ARE UNDERSTOOOD BY GENERAL CHEMI
1A STUDY OF HOW PRECURSOR KEY CONCEPTS FOR ORGANIC
CHEMISTRY SUCCESS ARE UNDERSTOOOD BY GENERAL
CHEMISTRY STUDENTS
- By Pat Meyer Western Michigan University
2Purpose of the study
- To determine how general chemistry students
understand the key concepts most likely to
enhance student performance in organic chemistry - Necessary preliminary step survey organic
chemistry instructors to find out what general
chemistry key concepts are most important for
their students to understand in order to do well.
3Literature Review
- A common error students make when they study
organic chemistry is sensing the difficulty of
the task before them and trying to memorize
results and algorithms. Students wrongly believe
that doing so gives them a sufficient grasp of
the field. Nahkleh Lowry Mitchell 1996. - Although the flashcard strategy will sometimes
work for a while at the beginning of a students
first organic chemistry course the belief in
this strategys appropriateness seems to stymie
student performance in the long run Bradley
Ulrich Jones Jones 2002. - The weaknesses of rote learning have been clearly
demonstrated in the literature Bodner 1986
Pendely Bretz Novak 1994 Pungente
Badger 2003.
4The Setting and the Research population
- Volunteers were solicited from one Fall section
and one Winter section of CHEM 110 a traditional
firstyear general chemistry course and
information was collected regarding their time
availability during the week. Random selection
was performed on the list of subjects who both
expressed interest and had a class/work schedule
complementary to that of the interviewer. - The majority of the potential participants in
this study were Caucasian Midwestern USA
students and approximately 1824 years of age. - They varied in the amount of previous
collegelevel science experience but the
majority of them had only a fairly small amount
or none at all.
5Instrumentation
- Covalent Bonding and Structure diagnostic
instrument Peterson Treagust Garnett 1989.
The instrument consists of multiplechoice
twotiered items. The first part of each item
asks about chemistry subject matter content
while the second part asks the subject to choose
from a list of reasons why he or she picked a
certain answer to the first part. - The second instrument the Geometry and Polarity
of Molecules diagnostic Furió Calatayud 1996
deals with many of the same topics. It is not a
twotiered instrument but rather a set of 16
single tier traditional multiplechoice
questions with three or four possible answers
given.
6Interview Protocol
- Subjects were videotaped while attempting to work
certain items and questions from the diagnostic
instruments during individual sessions ranging
from 45 minutes to an hour. - The subjects were encouraged to think out loud
during their efforts. They were required to use
a marker and large whiteboard for any scratch
work they did during the interview. - Probes were used when no commentary was given
and secondary probes were sometimes used if a
subject gave an interesting response to a certain
item or question. - Subjects were compensated by a 15 cash payment
and were encouraged by a bonus payment at the
end of the series an additional 15 if they
participated in all four interviews.
7Data Collection and Methodology
- Out of 19 subjects 16 completed all four
interviews eight in Fall and eight in Winter. - Subjects were asked 16 twotiered items and up to
16 singletiered questions during the four hours
of interviewing. Questions were grouped by key
concept during the interview sequence. - Transcription and coding procedures were
preformed on the raw data from the videotapes. - Lectures and the textbook were carefully studied
as a check. - When the correct and incorrect responses were
studied certain commonalities were found across
several subjects. These responses needed to be
grouped in some way to make the data more
manageable for analysis because there were
hundreds of responses and justifications
collected from the subjects
8Assertions 13
- Many students misunderstand the location and
nature of intermolecular forces. - Some think electronegativity differences among
atoms in a molecule are sufficient to make the
molecule polar regardless of spatial
arrangement. - Most know that higher phase change temperatures
imply stronger intermolecular attractions but
many do not understand the difference between
covalent molecular and covalent network
substances.
9Assertions 46
- Many have difficulty deciding whether a molecule
is polar or nonpolar often confusing bilateral
symmetry with spatial symmetry in all three
dimensions. - Many cannot reliably draw correct Lewis
structures due to carelessness and overuse of
flawed algorithms. - Many are confused by how electrons can both repel
one other and facilitate bonding between atoms
via orbitals this seems oxymoronic to them.
10Assertions 79
- Many cannot explain why the atoms of certain
elements do not follow the octet rule and some
believe the octet rule alone can determine the
shape of a molecule. - Most do know that electronegativity and polarity
are not adequate to determine the shape of a
molecule but some apply the VSEPR theory in
incorrect ways. - Students do not reason significantly differently
when working with various representations of
molecules such as ballandstick models
molecular formulas and Lewis structures.
11Generalized Commentary
- Subjects 4A 5A 8A 9A and 2B mentioned the
problem of exceptions in chemistry. It seems to
them that every time a rule is given it will
soon be broken making them question the value of
the rule in the first place. - Subject 4A noted that Every time you get a rule
theres always exceptions and the exception
doesnt follow the trend so you have to memorize
these thousands of exceptions. Like the Periodic
Table boron doesnt follow its bonding thing
[the octet rule] even the Periodic Table isnt
solid 4A110. - Subject 8A a fifthyear senior in expressing
frustration that this course was going to be the
first C grade she ever earned I want it to
click like everything else but it doesnt.
They give us a rule and they come up with 20
exceptions and heres why 8A230.
12Generalized Commentary
- Some subjects referred to the abstract quality of
the discipline. - Subject 4A explained how she felt the subject was
difficult because I cant see molecules
4A157. - Subject 8A spoke of the weirdness of chemistry
its out there like science fiction 8A123. - Subject 6B a secondyear biology major
contrasted his major field with chemistry in
explaining that biology is more handson and
doesnt involve things that are too small to
directly observe 6B112. He was apparently
unaware that molecular biology does focus on
things too small to directly observe.
13Further Research
- A worthwhile investigation would be to expand and
change the recruiting of subjects to focus on
current organic chemistry students. The
conceptual understanding of these students could
be statistically compared with their organic
chemistry exam scores to check the assumption
that high performance on the items of the
diagnostics really does correlate to high
performance in the organic chemistry examination
room. - Assuming there is a significant difference
between the performance of these two samples is
the difference between the conceptions of
preorganic and current organic chemistry
students merely a matter of degree i.e.
refinements of ideas or does it reflect dramatic
paradigmshifts Kuhn 1970 in the subjects
thinking? - Another expansion of the research sample to
include organic chemistry researchers in academia
and industry. How would their performance and
conceptions of the key ideas compare with that of
students? The possibility exists that the key
ideas revealed in the survey are not necessarily
essential for high organic chemistry performance
in career situations
14Acknowledgements
- My family James Barbara and Frank Meyer for
their caring expressed in so many ways. - William Cobern Marcia Fetters Heather Petcovic
and Elke Schoffers for sharpening my writing and
thinking. - Debra Stoyanoff and William Merrow for
administrative and technical support
respectively. - My close friends Brian Nolan and Kimberly Jack
for listening and giving solid advice during my
data collection and writing - My wife and best friend Cindy Meyer for her
patience helpfulness and confidence in me. Mere
words can neither explain nor quantify how
grateful I am for her role in my endeavors.
15Works Cited
- Bodner George M. 1986. Constructivism A
Theory of Knowledge. Journal of Chemical
Education 63 10 873878. - Bradley Alexander Z. Ulrich Scott M. Jones
Maitland Jr. Jones Stephanie M. 2002.
Teaching the Sophomore Organic Course without a
Lecture. Are You Crazy? Journal of Chemical
Education 79 4 514519. - Furió C. Calatayud M. L. 1996.
Difficulties with the Geometry and Polarity of
Molecules Beyond Misconceptions. Journal of
Chemical Education 73 1 36 41. - Kuhn Thomas S. 1970. The Structure of
Scientific Revolutions 2nd edition. The
University of Chicago Press Chicago p. 1011. - Nahkleh Mary B. Lowry Kirsten A Mitchell
Richard C. 1996. Narrowing the Gap between
Concepts and Algorithms in Freshman Chemistry.
Journal of Chemical Education 73 8 758 762. - Pendley Bradford D. Bretz Richard L. Novak
Joseph D. 1994. Concept Maps as a Tool To
Assess Learning in Chemistry. Journal of Chemical
Education 71 1 9 15. - Peterson Raymond F. Treagust David F.
Garnett Patrick 1989. Development and
Application of a Diagnostic Instrument to
Evaluate Grade11 and 12 Students Concepts of
Covalent Bonding and Structure Following a Course
of Instruction. Journal of Research In Science
Teaching 26 4 301314. - Pungente Michael D. Badger Rodney A. 2003.
Teaching Introductory Organic Chemistry
Blooming beyond a Simple Taxonomy. Journal of
Chemical Education 80 7 779 784.