last updated Fri, Sep 27, 2002

Problem set #2 (Meeting 2)


ATTN: answers to the below questions are due at the start of your lab period; these answers should be part of your pre-lab write-up.


1. What drives the reaction towards the elimination product?

2. What is the expected alkene product formed from the dehydration of the following alcohols? Show major products only. help

3. What qualitative tests will be carried out in this experiment to determine the presence of a double bond in the final product? Show the equations including the proper stereochemistry of the products.

4. What are the most important changes in the IR spectrum going from cyclohexanol to cyclohexene (functional groups and wavenumbers)?

5. What is the function of the following compounds/equipment in the elimination experiment?

a. cyclohexanol

b. sulfuric acid

c. sodium sulfate

d. Hickman head

6. What is the function of the sodium hydroxide solution in the benzoin experiment?

7. Why is it important to use fresh benzaldehyde? How can you purify benzaldehyde? (Hint: What happens if you store aldehydes for longer time?)

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

a. Use the alcohols and their protonated forms that you drew last week for this exercise.

b. Select Calculations from the Setup menu.