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Colleen Fried |
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May 23, 2003 |
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NOCHE IT Committee |
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JiTT |
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Developed at Air Force Academy, IUPUI, Davidson
College for their Physics program |
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http://webphysics.iupui.edu/jitt/jitt.html |
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Receive timely delivery of pertinent information |
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Increase interactions with faculty |
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Take control of their own learning |
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Gain problem-solving skills and conceptual
understanding |
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Develop their: |
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Critical thinking ability |
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Ability to frame and solve problems |
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Teamwork and communication skills |
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Warm-up or Preflight |
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Puzzles |
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Java applets – concept tests, homework, prelabs,
in-class demonstrations |
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What’s x good for? |
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This week in… |
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Pre-class assignment |
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Three questions |
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Explain |
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Predict |
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Multiple choice |
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Graded on thought process |
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Student Preparation |
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Safety considerations |
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What safety concerns are there in today’s lab,
and how will you deal with them?
What will you do with the waste you generate? |
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Being conversant with the full protocol |
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Your lab procedure calls for you to monitor your
reduction reaction using TLC.
Provide a description of how you intend to accomplish this. |
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Applying techniques to new situations |
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After isolating the crude benzocaine, the lab
procedure calls for you to recrystallize your product using an
ethanol/water solution. What is the
purpose of recrystallization, and how much solvent will you need to use if
you isolate 0.425 g of crude benzocaine? |
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Analysis of data |
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At the end of the lab, we will analyze the
product composition by GC-MS (a mass spectroscopy technique). Based on the minimal introduction to
mass spectroscopy you've received, how might you tell the starting ketone
from the product alcohol? |
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Insuring students obtain appropriate/sufficient
data |
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A pair of Chemistry 320 students ran a
bromination reaction of diphenylether, and found that the bromine color had
disappeared by the time they got the cuvet into the spectrophotometer. How
should they proceed with the experiment? |
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Move beyond cookbook |
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The following is a table of Rf values
for compounds A and B. Which
solvent would be the best solvent to use if you wished to separate these
compounds using TLC or a related chromatography? Explain. |
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A B |
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Hexanes 0.15 0.22 |
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Diethyl ether 0.28 0.46 |
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Acetonitrile 0.58 0.69 |
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Use of Symbols |
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Use of symbols sometimes masks misunderstandings |
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Students try to rely on memorization |
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Students coast in the beginning |
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Knowledge builds rapidly and is dependent on
prior knowledge |
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Ask students to translate the symbols into
verbal explanations |
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Ask students to apply knowledge |
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Reinforce critical concepts early and often |
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Insure students master concepts as they are
covered |
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8/30/00: Use a pen(cil) and paper to draw as
many isomers of C5H12 as you can. How many did you draw? Describe each structure in your own
words. |
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10/6/00: Use a pen(cil) and paper to draw all of
the isomers of C4H10O. |
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a.
Give the IUPAC name for each compound. |
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b.
How many signals in the 13C NMR would you expect for each
of these isomers? What is the
approximate location of each signal? |
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One reaction we haven’t talked about yet is
the Fischer esterification reaction.
In this sequence, a carboxylic acid is converted to an ester in the
presence of an alcohol and an acid catalyst. Propose a reasonable mechanism for the following
transformation. Remember the
mechanism for acetal formation. |
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Student answers are compiled in one document for
rapid assessment |
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Student answers can be anonymous (or coded) |
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Warm-ups for the semester can be posted in the
beginning |
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Responding to individual students is not easy |
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Isn’t dependent on a web server. |
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Easy to reply individually to students (a laptop
is a big help here) |
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Easy to save individual responses |
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One folder for each warm-up |
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One folder for each student |
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Each e-mail must be opened individually |
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Students were immediately comfortable
approaching me |
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Student
participation in class was overwhelming |
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Students seemed to move beyond memorization |
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There were fewer problems with fundamentals |
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ACS Organic final exam results |
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year(s) 1998-2000 2001/2003 |
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#tests 59
28/19 |
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median 35
39/41 |
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nat. rank 40% 54%/60% |
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36 43% |
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