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WRAD: Writing Guide for Chemistry |
Table
of Contents
Resources for help with writing
General guidelines for writing reports
Presenting data... the good, the bad, and the ugly
Resources
for help with writing
1. It may
seem obvious, but remember that your instructors are there to help. Did they
provide handouts or online information with specific instructions on style,
format, and a checklist of items to include in the report? Since expectations
will vary from class to class, and sometimes even from report to report, it is
important to understand what is being requested before organizing your results
and beginning to write. A grading sheet specifying the number of points or relative
weight given to each part of the report can help you to focus your
efforts. Find out if your instructor
will provide these in advance.
2. The ACS Style Guide,
A Manual for Authors and Editors, 2nd ed. (Dodd, J., Ed.;
American Chemical Society, Washington, DC, 1997) is an excellent resource with
writing tips and detailed descriptions of the ACS writing conventions. The
guide can be ordered at http://www.oup-usa.org/j778/isbn/0841234620.html.
3. Some handy online resources:
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100 + online writing labs (short
instructional pages) |
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Links about scientific and
technical writing |
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General guide to grammar and
writing |
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An online course in science and
technological writing |
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Guide to writing a thesis or
dissertation |
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Links from the OSU writing center
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http://osu.orst.edu/dept/writing-center/resources.html |
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Handling electronic
references |
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General
guidelines for writing reports
As noted
above, instructors differ in their expectations for lab reports. This is
reasonable when you consider that there is also a wide variation in the
requirements for different chemistry journals and publishers. Even so, a long
experience in reading lab reports, papers, and thesis drafts indicates that
there are common areas of confusion for many students, and therefore we provide
a few general guidelines to help in creating reports or publications.
1.
Use the correct verb tense
Lab reports
and research papers should be mainly written in the present tense. You should
limit the use of the past tense to (1) describing specific experimental methods
and observations, and (2) citing results published in the past. The following
sentences can be written in the past tense:
The solid was washed with water, then dried
overnight in a dessicator.
Jones et al found that polymers with
absorption maxima between 200 and 300 nm degraded when exposed to ultraviolet
radiation.[1]
Data analyses, on the other hand,
should be written in the present tense:
Extrapolation of the line in Figure
3a gives a polymer viscosity of 40.2 cp: an error estimate using eq. 2 provides
an uncertainty of 0.4 cp.
2. Write in the third person
A common question is whether the words
I, me, my, we, our, or us, belong in
science writing. Because scientific experiments demonstrate facts that do
not depend on the observer, reports should avoid using the first and second
person. For example, the second sentence below is better because it avoids the
use of the first person:
I stirred the solution for 2 h;
then I obtained a yellow powder by filtration.
Stirring the solution for 2 h,
and subsequent filtration, yielded a yellow powder.
However, when referring to your own
results or conclusions, it can be simpler and clearer to use the first or
second person:
While Smith and Jones report a cell
dimension, c, of 23.3(1) Å, the authors’ own data indicate a value of
23.6(1) Å.
Smith and Jones report a cell dimension, c, of 23.2(1) Å, but our data
yield a value of 23.6(1) Å.
The “authors’
own data” is an awkward phrase and “our data” in the latter sentence is
better.
3. Be clear but concise
Reports
and papers should fully describe experiments in a precise and factual manner.
Both the depth of the error analysis and the writing style must be appropriate
to this task. Consider the following sentence in a discussion:
The
calorimeter vibrated a little, but it is still easy to measure the peak in
Figure 1 very accurately.
Words and phrases such
as “a little”, “easy”, and “very accurately” have no definite meaning, and are
therefore inadequate. Quantitative, or semi-quantitative, descriptions and
analyses are always preferred over the use of such imprecise terms. In the
following rewrite, the error is much more clearly described:
The
largest source of error is vibration, which is estimated at 1–5 W/kg RMS. This
adds at most a 4% uncertainty to the peak integration, and values obtained are
therefore reported as +- 4%.
Although you should strive to describe
experiments in sufficient detail to be reproduced, it is also important to
write concisely. Often, text can shortened by condensing or rephrasing
without decreasing the meaningful content. In the two examples below, the
latter conveys the same information in a more concise, and preferred, writing
style.
Distillation fractions
three and four were combined in a 100ml round-bottom flask. To this flask was added 1.966g (0.0114 mol)
of benzoic acid. The flask was then
connected to a long column, distilling head, and condenser. Glass-wool and foil was again wrapped around
the column and distilling head.
In a 100 mL round
bottom flask equipped with a water jacketed condenser and wrapped column and
head, 1.966 g (0.0114 mol) of benzoic acid was added to the combined third and
fourth fractions.
4.
Revise and proofread
Treat your first written copy as a
draft, and then read through and revise. In WIC courses, some assignments will
have revision steps included in the submission and grading process. Many
students are surprised at how many simple errors can be found in first drafts,
and how much their writing improves after using this simple method. A final
proofreading is also important, and can help to minimize spelling and
typographical errors. A few minor errors are almost inevitable in any written
document, but reviewers, and instructors, can usually tell when they are
reading a first draft. Along with a “human” proofread, use a spell check
routine to help spot errors.
Presenting
data...the good, the bad, and the ugly
Reports should usually include a narrative text
that describes and explains the information presented. Use the results section
to explain the purpose of every figure, schemes, equation and table. Published
research results never include “orphan” data, that is, information that is not
explained or put into context by the written text. This is also a good rule to follow in lab reports.
When referring to a figure, table, or
equation, use its number in the text, for example:
A plateau
was observed at reduced pressures greater than 0.1, as indicated in Table 1.
It follows that every figure, table
and equation needs a number. Figures and tables require a caption that includes
the number and a descriptive title:
Figure
1. Mass uptake vs. reduced pressure for
Zeolite 5A.
Table 1. Powder Diffraction Data Obtained for Zeolite 5A.
Note that the labels “chart” and “graph”
are somewhat antiquated terms, and have been largely replaced by “figure”.
Equations will normally have a number placed in parentheses at the right
margin:
E = mc2 (1)
Here are some additional tips for
preparing figures and tables:
Ø
All graph axes require labels that include
both the variable name and units.
Ø
Axes
should use reasonable scales to clearly show the data and have labeled tic
marks. The axis labels do not need to show the full number of significant
figures.
Ø
Table
columns should specify the units employed under each heading.
Instructors
(and editors) can be picky about writing conventions. Literature citations,
symbols, and abbreviations all require strict adherence to a standard format.
Unfortunately, the particular standard used varies between publishers. An
important standard is that adopted by the American Chemical Society (ACS), and
this will be used by many chemistry lab courses at OSU. It would be quite
difficult to memorize all the forms for literature citations alone.
Fortunately, there is no need to do so. The ACS Style Guide (see above) lists
all the required formats and provides easily-followed examples. Nevertheless,
it’s useful to be familiar with the most common citation formats and
abbreviations. Some frequently-used ACS formats are provided below.
For journal
articles:
1.
Bode, H.; Jenssen, H.; Bandte, F. Angew. Chem. 1953, 65, 30.
Note – “65” is in italics
and refers to the volume number, and “30” is the first page of the article.
For books:
2.
Dresselhaus,
M.; Dresselhaus, G.; Eklund, P. Science of Fullerenes and Carbon Nanotubes;
Academic: New York, 1996; pp 126-141.
3. Watanabe,
N.; Touahra, H.; Bartlett, N.; Mallouk, T. Fluorine Intercalation Compounds of
Graphite. In Inorganic Solid Fluorides:
Chemistry and Physics; Hagenmuller, P., Ed.; Academic Press: New York,
1985; pp 331-369.
For websites:
4.
Oregon State University Chem 462
Lecture Notes. http://www.chem.orst.edu/ch411/ch411cn.htm
(accessed May, 2000).
In the sciences, results are usually discussed in relation to the
work of others. Your writing will therefore often refer to results or
conclusions that are not your own. This is fine as long as you clearly
distinguish between your results and those obtained from other workers or the
literature. Each time outside results are cited, a reference must be provided
to the original source.
A related issue lies in the use of
quotes from another work. The exact duplication of text from an outside source
is acceptable only if it is placed in quotations and a reference provided.
Paraphrasing or summarizing other results can also be acceptable if a reference
is provided. However, incorporating
another author’s words or style into your own writing is not allowed, even if
the original work is referenced.
When there are group assignments or
reports, make certain that you understand the instructor’s expectations for
shared vs. individual contributions. Students often do experimental work in
groups, and are encouraged to discuss the lab results and data analyses with
others. However, report writing is most
often expected to be an individual effort.
The following are all examples taken from
student reports in OSU chemistry. In each case, a revised version follows the
original text. For practice, read each original text, then compose a revised
version before reading the one provided.
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1. |
Original
text: |
Distillation fractions three and four were combined in a 100ml
round-bottom flask. To this flask was
added 1.966g (0.0114 mol) of benzoic acid.
The flask was then connected to a long column, distilling head, and
condenser. Glass-wool and foil was
again wrapped around the column and distilling head. |
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Revised
form: |
In
a 100 ml round bottom flask equipped with a water jacketed condenser and
wrapped column and head, 1.966 g (0.0114 mol) of benzoic acid were added to
the combined third and fourth fractions. |
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2. |
Original
text: |
Next the copper solution was prepared. This was done by weighing
out 0.1821 g of copper nitrate and diluting it in 10mL of tap water. |
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Revised
form: |
A
solution was prepared by dissolving copper nitrate (0.1821 g) in tap water (10
mL). |
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3. |
Original
text: |
If for example, we could have used a red and green apple to
determine the components, we could have averaged the data and obtained more
accurate results. |
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Revised
form: |
If,
for example, data were obtained from both a red and a green apple, the
averaged results could provide more representative values. |
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4. |
Original
text: |
This experiment intends to investigate upon any measurable
amounts of Nickel in the surrounding mud area and within barnacles living on
the pilings. |
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Revised
form: |
The
purpose of this experiment is to determine the nickel content in the
surrounding mud area and in the barnacles living on the pilings. |
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5. |
Original
text: |
For the final yield of pentene isomers, only the elimination
sample was considered…The yields are reported in Table 2-3. |
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Revised
form: |
The
calculated final yields of pentene isomers (Tables 2 and 3) are based on the
elimination step only. |
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6. |
Original
text: |
The contents of the flask were poured into a separatory funnel,
and mixed with increasing vigor. The
evolving gas was vented periodically.
The product was allowed to separate into two distinct layers. The bottom, aqueous, layer was bright
yellow. The top, ether, layer was
reddish-brown and transparent. Each
layer was decanted into separate containers.
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Revised
form: |
The
product was transferred to a 1 L separatory funnel and upon mixing separated
into a bright yellow solution (bottom layer) and a clear ethereal
reddish-brown layer with the evolution of carbon dioxide. |
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7.
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Original
text: |
The final solution was cooled using an acetone-ice bath. A temperature of -5 C was necessary to
avoid the decomposition of the diazonium salt. Hypophosphorous acid and sodium nitrite were slowly added. |
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Revised
form: |
To avoid
the decomposition of the diazonium salt, the resulting solution was cooled to
-5 °C using an acetone-ice bath and then hypophosphorous acid and sodium
nitrite slowly added. |
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8. |
Original
text: |
The contents of the flask were poured into a separatory funnel,
and mixed with increasing vigor. The
evolving gas was vented periodically.
The product was allowed to separate into two distinct layers. The bottom, aqueous, layer was bright
yellow. The top, ether, layer was
reddish-brown and transparent. Each
layer was decanted into separate containers.
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Revised
form: |
The
product was transferred to a 1 L separatory funnel and upon mixing separated
into a bright yellow solution (bottom layer) and a clear ethereal
reddish-brown layer with the evolution of carbon dioxide. |
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9. |
Original
text: |
The first part of this experiment was to determine the percent
removal of lead, calcium, magnesium, and copper. We had thought that there was not enough lead and copper left
after we filtered the tap water, so two spiked solutions were made. |
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Revised
form: |
The
purpose of the first part of this experiment is to determine how effectively filtration
removes lead, calcium, magnesium, and copper from tap water. Although low levels of the metals were
accurately detected in spiked solutions, no detectable Pb or Cu was found in
the filtered sample. |
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10. |
Original
text: |
This should have given us a 5.00ppm solution instead the ICP
data showed that we had a 1.373(+/-0.0374)ppm. We decided that we would use the ICP data for all our
calculations. |
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Revised
form: |
ICP
data indicated that the solution prepared to contain a Pb concentration of
5.00 ppm actually contained 1.373 +/- 0.037 ppm. The ICP values were used in subsequent calculations. |
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11. |
Original
text: |
The standard addition for the tonic water was done by using the
tonic water solution and doing a 1 to 10mL dilution on it with the sulfuric
acid. A signal was obtained for the
sample. After the first signal was
taken 15μL of 10ppm quinine sulfate stock was added, the signal was then
taken. |
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Revised
form: |
For
the standard addition measurement on tonic water, first a tonic water test
solution was diluted 1 to 10 with sulfuric acid in a 10 mL volumetric. The
absorbance was measured before and after 15 μL of a 10 ppm quinine
sulfate stock solution was added to the cuvette. |
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12. |
Original
text: |
It was observed that the barnacle sample was very well digested,
but minute traces of sludge were still found in the mud cell. Indications of this left over sludge may
be from silicon waste left in the sand and could not be further digested with
the acid used. This silicon waste was
found to be negligible due to the belief that all of the existing Nickel on
the silicon was dissolved by the HNO3. |
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Revised
form: |
The
barnacle sample was very well digested, but minute traces of particulates
remained in the mud cell. These particulates are assumed to be silica from
sand since all other known components dissolve in nitric acid. |
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13. |
Original
text: |
The following standard concentrations were used to follow Beer’s
law for the absorbances at the corresponding wavelength: (Table) |
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Revised
form: |
The
standard concentrations were measured at the corresponding wavelengths and
the data provided in Table 1. |
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14. |
Original
text: |
Some changes were made to this procedure with one of them being
that the absorption corresponding to the galactose was not found for both
sample sets. ...Another change is
that the final absorption readings were taken 20 minutes after adding the
final enzyme, β-galatose dehydrogenase, instead of 15 minutes. |
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Revised
form: |
One
change made to the written procedure was that the absorbance due to galactose
was not obtained for both sample sets. ..... A second change
was that the final absorbance
measurement was made at 20 min instead of the suggested 15 min after adding β-galatose
dehydrogenase. |
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15. |
Original
text: |
Twelve penny solutions were analyzed using flame atomic
absorption, and this data was used to construct a calibration curve for each
metal. |
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Revised
form: |
The
twelve solutions obtained by dissolving pennies were analyzed using flame
atomic absorption spectrophotometry, and these data were used to construct a
calibration curve for each metal. |
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Credits:
Oregon State University Chemistry Dept.