IB Chemistry IA Lab Report Guidance
IB Chemistry IA Lab Report Guidance
This should show evidence of curiosity, personal and initiative – even if it just relates
to straightforward IB Chemistry syllabus coverage.
Key phrases:
“I wondered if…”
“I can imagine that… this might lead to …”
Needs to be focused and relevant. It is best to phrase this as a question; make sure
that your independent and dependent variables are clearly identified.
Avoid the use of vague terms such as `efficiency' and `suitable'. Remember
that in chemistry the word `amount' refers to amount of substance in moles.
Can I extract X from Y? is not likely to be very successful (no quantitative data)
Which brand of X contains the most Y? is not likely to produce sufficient quantitative
data, and anyway is of commercial concern rather than chemical concern
Method:
Must be clearly outlined (detailed enough that someone else could follow it).
Include a labelled photo or diagram of your equipment especially if you have used
a non- standard method or adapted a standard one.
The rationale behind the method should be included:
What options for method were there?
Why was this method chosen?
Why were these stoichiometric quantities / concentrations chosen? (Prior trials,
theoretical calculations).
In the middle box you could draw a distinction between the proximate variable
(e.g. the variable you actually measure such as time for a colour change) and the
ultimate variable (the thing you actually want to know, after processing, such as
relative rate of reaction).
A common error is to identify variables in a list and then not address them
explicitly in the method.
Recording Raw Data (actual measurements recorded in lab):
Data tables need informative titles outlining what the data is (i.e. not just ‘Table
1’). All columns labelled with variables, units (in headings) and uncertainties (in
headings). Variables in full (‘initial rate’ not ‘rate’; ‘time for colour of iodine to
disappear’ not ‘time’). Record numerical data and errors to the correct no of
sf/dp. Report data with academic integrity (honesty).
QUALITATIVE data also included, ie, relevant observations, with your raw data.
VALUES of controlled variables should be included (e.g. don’t just assume room
temperature for all solutions)
Explain your rationale for estimates of uncertainties: e.g. I have used twice the
smallest increment or I’ve chosen the mid point of the data set or I’ve estimated
the time uncertainty as 0.5 s as a reasonable reaction time
Graphs obtained using a sensor which show no processing are raw data.
Data obtained from secondary sources:
If you follow this route, DO NOT ASSUME that all errors/uncertainties are
negligible.
There are likely to be discussion points surrounding the limitations of the data and
the methodology used.
Similarly, do not assume there are no ethical concerns surrounding data. Where is
it from? Who is it available to?
Ensure numerical data has been appropriately and correctly processed and units
shown in a sample calculation (otherwise this will impact on your conclusion).
Absolute uncertainties should be stated to 1 s.f. (if random uncertainty more than
2%) but 2 s.f. (if random uncertainty more than 2%).
The related quantity should be rounded to the same degree of precision, e.g. 24
±0.05 cm3 is incorrect, 24.00 ±0.05 cm3 is correct.
Generally speaking, standard deviation calculations and t-tests are not appropriate
in most chemistry analyses.
Identify any outliers and decide how to treat such data points.
In raw data, sig figs should be consistent with the quoted uncertainty, and should
be consistent within a given column. (Don’t write the uncertainty is 0.1 cm3 and
then quote figures to 0.001 cm3.)
In processed data, sig figs should be consistent with the uncertainty propagated to
obtain that data. (If the total uncertainty is 10%, you can’t quote 5 sig figs in your
answer.)
Presentation of Data (Graphs etc):
Axes labels, graph titles (NOT ‘graph 1’, but a meaningful title).
Don’t assume MS Excel will give you the best marker points (they are usually too
large), scale, axes, trendline etc. All these things can be edited. If in doubt draw it
by hand and scan it in.
Analysing Data:
If you need to describe it in some detail, then do so: At values of X below 10, Y
increases steadily with X. At higher values of X, the increase of Y slows down.
Remember the graph line is your final statement of the pattern, NOT the raw data.
One useful purpose of error bars is to help you determine a plausible maximum
and minimum gradient for your data.
Interpretation of Conclusions/Analysis:
You may be trying to establish a known relationship between variables. You can
apply theoretical chemistry to this. HOWEVER, if your data doesn’t quite fit, think
about reasons (non-standard conditions, other confounding variables, etc).
If your investigation is open-ended and you really don’t know the ‘right’ answer –
it is OK to speculate. Often there are multiple plausible explanations, which might
lead to different answers. Sometimes several factors are at work, pushing the data
in different directions. Don’t overstate any apparent trends.
Consider the reliability (precision) of your results between trials and the validity
(accuracy) of your results in comparison to the literature (or manufacturer's
value(s)) or background theory (if any).
Determine whether your answer is close enough to the literature value (within the
limits of your random uncertainties). If it is not – you should suggest possible
systematic errors.
Were there any methodological issues that prevented you reaching a firm
conclusion?
Many students only identify procedural weaknesses (why the planned method was
not properly implemented); be sure to identify any relevant methodological
weaknesses (why the designed method itself was flawed or limited).
Identify and evaluate the relative magnitude of the major source(s) of random
and/or systematic error.
This should focus on reducing the magnitude of the major source(s) of random
and/or systematic error.
Classic wrong answer: You establish that the random uncertainties only account
for a 2% error. However, the answer you achieve is 25% away from the literature
value. It is therefore POINTLESS to assert that decreasing the random uncertainty
(e.g. with more precise glassware) is worthwhile. Instead you should be looking for
systematic uncertainties.
Extensions to the Investigation:
What could you usefully do to extend your investigation? Other variables, more
data within a certain range, alternative method?
Communication
Structure of report
Ensure that your method contains sufficient detail that another student could
repeat exactly what you did to obtain similar results.
Your report must contain at least one worked example calculation (including
error analysis), so the reader can understand how the data was processed.
Ensure that terms such as amount (moles), mass and weight are used correctly.
Technical aspects and conventions
Take care with labelling graph axes, use of units, decimal places and significant
figures.
Ensure that APA citations (both in-text and in the Works Cited list) are
handled correctly.
Carefully check that chemical formulas, equations (with state symbols) and units are
correctly formatted (superscripts, subscripts ,etc.).
If you are having difficulty sourcing the information you need, you could
try posting a descriptive question on a question and answer site like the
Chemistry Stack Exchange or Quora.