Chemistry 351 - Principles of Organic Chemistry II
  Spring Semester 2015, Winona State University, Dr. Thomas Nalli

Guidelines for Lab Reports

Learning how to effectively report experimental results is extremely important in all of the sciences. Although the customary format may vary between discipline, a scientific report should be clear, thorough, concise and well organized and should make effective use of tables and graphs.

General Guidelines

Formatting

  • Reports should be word-processed and double-spaced.
  • Do not ignore the need for subscripts and superscripts in chemical formulas. These are easily available in all modern word processors.
  • Use a minimum font size of 11 and left and right page margins of 1.0".

Conciseness

  • Strive to make your report as concise as possible. A page limit of 12 pages (not counting attachments) applies to all lab reports. (Please number the pages!)
  • In achieving conciseness, it is important that you use standard abbreviations and/or chemical formulas where possible in place of full chemical names. For example write "MeOH" instead of "methanol" and CDCl3 instead of chloroform-d.
  • All measurement units have standard abbreviations and these should always be used in conjunction with the numerical value for the measurement, e.g. always write "15 cm" not "15 centimeters" or "fifteen centimeters".
  • Here is a spreadsheet with commonly needed standard abbreviations. Remember to use these freely and to not waste space defining them.
  • Also consider creating your own abbreviations to replace long compound names. Define these simply by placing parentheses immediately after the first instance of the full compound name in the report.

Data Interpretation

  • Students are encouraged to bring rough drafts and questions about data interpretation to the instructor prior to submitting their final report. (Unless otherwise announced in lab.)

Organization

Title Page

  • Give the number and title of the experiment, your name, course number and section, and the date submitted.

Purpose

  • Give specific information on the reaction being carried out including chemical equations showing structures of all reactants and products.

Mechanism

  • Present and discuss the accepted mechanism for the reaction carried out. Make sure to use equations/structures/curved arrows as necessary to show the mechanism properly.

Results Tables

  • Present all of the results of the experiment in table form.
    • Try to make your results tables as concise and well organized as possible.
    • Number and title your tables. The title should give fairly complete information about the data contained in the table.
    • Include structures of the compounds in the tables.
  • Include the absolute yield (mass), theoretical yield, and percent yield (rounded to the nearest whole number) of any product obtained. (Show the calculation of theoretical and percent yield on an attachment.)
  • A melting point range should be reported for every crystalline solid product.
  • Include literature values for any physical constants measured. 
  • Make sure to give units where required. (A well-organized table gives the units in the column headings rather than repeatedly throughout the table.)
  • Also include summaries (i.e., peak listings) of any spectroscopic data (NMR, IR, MS) obtained.
    • Round off IR frequencies to the nearest 1 cm-1 and MS peaks to the nearest 1 m/z unit. Carbon NMR peak shifts should be rounded off to the nearest 0.1 ppm except when greater precision is needed to distinguish closely spaced peaks. (These guidelines are taken verbatim from the Journal of Organic Chemistry's guidelines for authors.)
  • Do not include solvent peaks (e.g., CDCl3) in NMR tables.
  • Do include literature values of chemical shifts, wavenumbers, and m/z when available.
  • For NMR, IR and MS tables you should include a column for "peak assignment".
    • For NMR the assignment should be a letter that refers to a labeled chemical structure included with the table.
    • For IR the assignment should refer to the specific type of bond vibration and the functional group family, e.g., C=O (ketone), C=O (anhydride), O-H (alcohol).
    • For MS, the assignment can take form of describing the neutral fragment lost, e.g. M - CH3, M - Br, or preferably show the structure of the cation detected
  • Make sure to observe the significant figures convention! Significant Figures Tutorial
  • Use footnotes as necessary to fill in missing details or to give definitions of abbreviations used in the table.
  • Also use footnotes to give references for literature values. (Refer to each reference by its number in your report-end list of references. For example a table footnote might typically read, "See reference 3.")

Results and Discussion 

  • Start by presenting key results from the results tables briefly in a non-interpretive way. Point out the most important take-home points from the table and/or any trends you would like to draw attention to.
  • Go on to explain your interpretation of these results. Your main aim is to show how they support the theories presented in the background.
  • Make liberal use of structural diagrams, equations, curved arrows, images of molecular models, etc., to illustrate points being made as appropriate.
  • For puzzling results that do not seem to fit the theoretical expectations, are there valid explanations for them? Are they erroneous (due to systematic experimental error) (identify the specific reason for the systematic error if you think it is present). If you can rule out systematic error then examine how the theories could be modified to accommodate the results.
  • This section should include answers to the assigned questions. Make sure to explain all answers completely even if the question does not ask for an explanation. 
  • Above all, make sure your answers and interpretations make sense! Do not just take a stab at interpreting the results! If uncertain, do some Internet and/or library research or ask the instructor if you are on the right track.
  • For synthesis experiments always discuss:
    • Yield - Actual yield of product versus the theoretical yield (percent yields) and possible reasons for loss of yield. Please see this page for more info: Yield Reporting and Discussion
    • Spectra Interpretation - Evidence for the structure of the product from NMR, IR and/or chemical tests.
    • Purity - Purity of the product as indicated by mp, bp, NMR,  etc. Identify impurities that are present if possible, explaining thoroughly the reasoning behind your conclusions.

Summary

  • Reiterate the main points from your results and discussion sections in very brief form. Ideally, you can boil down the experiment to four or five main conclusions, each stated in one or two sentences.
  • Give actual data again in this section to support each conclusion. The data can be concisely included simply by providing it in parentheses at the appropriate places within the text.
  • Comment on whether the experiment was successful or not and feel free to make suggestions as to how the experiment could have been better designed or carried out.

References

Attachments

  • Calculations - An example of each non-trivial calculation, including % and theoretical yield calculations, should be shown. Do not include trivial calculations such as subtraction of tare weights.

  • Spectra - Attach printouts of all spectra obtained. Make sure the spectra are completely labeled (name, date section number, expt number and title). All peaks should always be labeled. By labeling all solvent peaks and other expected extraneous peaks (e.g., TMS, water, CHCl3) you make clear what they are without unnecessarily devoting lab report discussion to them.

Product Submission

  • Products are ordinarily submitted for grading and then proper disposal. Submitted products should be fully labeled with the compound name and structure, your name, experiment number, and course number.
  • Solid products should be placed in small 2"x2" zip-lock baggies.
  • Liquid products should be placed in screw-top vials (not conical vials or reaction flasks).

Team Contribution Surveys (TCSs)

  • These are made available on D2L the same day the lab report is due for each experiment. They are due within one week of the lab report submission.