Meeting 3 Problem Set - 30BL

NO ONLINE QUIZ FOR THIS MEETING!

1.Using PC Spartan 2002 at the Science Learning Center (4th Floor Young Hall) do the following:

a. Draw camphor if you have not done it yet (Make sure that all hydrogen atoms are still attached!). Minimize the structures by clicking the minimize icon, , then save.

b. Go to the view mode by clicking the view icon, . Once in the view mode, click the Model menu and select Tube.

c. Select Calculations from the Setup menu.

The following window should appear. Select the options shown.



Verify the Charge is Neutral and Multiplicity is Singlet. Click OK.

• Select Submit from Setup menu.

  
  

  Under the Setup menu, select Surfaces. A window should appear. In this window click Add.

  

  A second window should appear. In this window, select the following

  

  Then click OK to exit dialog. Close the previous window.

  Select Submit from Setup menu. When the calculation is completed you will be notified.

  Under the Display menu, select Surfaces.

  

  A window should appear. In this window check the yellow box.

  

  Next, select the molecule by clicking on it. In the bottom right corner of the window, change the selection from Solid to Transparent.

d) Do the same (steps a-c) for 2-norbornanone.

2. Referring to the below reaction,

(endo/exo huh?)

answer the following questions:

a. Which isomer is expected to be the major product for this reaction? Why? (Include the LUMO diagram generated in question 1 to answer this question. Make sure to show the proper orientation! Hint: What are you trying to show here?)

b. What would change if NaBD₄ and CH₃OH/H₂O were used in this reaction? Show the structure of the product.

c. Why is the LUMO orbital used to rationalize the stereochemistry in this reaction?

3. Referring to the below reaction,

answer the following questions:

a. Draw the products formed in this reaction

b. Which product is the major and which is the minor? Explain using the LUMO generated above (Include the LUMO diagrams generated in question 1 to answer this question. Make sure to show the proper orientation!). What are the differences compared to 2-norboranone?

4. Experimental

a. Why is camphor dissolved in methanol first and the sodium borohydride is added later?

b. Why is important to avoid the evaporation of the methanol during the reaction?

c. After the reaction is completed, the reaction mixture is chilled and water is added. Why is this step performed and what is he supposed to observe at this point?

d. In lecture it was emphasized to minimize the amount of drying agent being used. Explain why. How does the student know that he added enough?

e. Why is the solvent evaporated on a water bath and not on the hotplate?

f. A student observes a melting point range of 210-212 ^oC for his final product in this reaction. Which conclusion(s) can he draw?

g. Why is it important to submit a fairly dilute sample for the acquisition of the GC?

h. How do the FTIR spectra of camphor and isoborneol differ from each other?