last updated Monday, October 09, 2006

Meeting 3 Problem Set - 30BL

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

a. Draw camphor if you have not done it yet (Make sure that all hydrogen atooms 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.

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 diagrams generated in question 1 to answer this question. Make sure to show the proper orientation!)

b. What would change if LiAlD4 and H2O were used 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!)

4. Methanol was used as solvent in the reaction. Which problem does this solvent pose for the reaction? How are the problems minimized?

5. How many grams of camphor can be reduced with 0.150 g of sodium borohydride (in theory)? Show pertinent chemical equation and calculations.

6. After the reaction is completed, water is added to the reaction mixture. Rationalize this step.

7. The crude product is redissolved in diethyl ether. Why is this step performed?

8. In which way does the melting point help to identify the compound and establish the purity of the sample?

9. Why is it considered poor lab techniques to leave bottles and containers open?