Organic Chemistry II
	Professor Carl C. Wamser
Chem 335 - Winter 2005	Exam 2

1. (15 points) Write complete names for each of the following, including stereochemistry if it is specifically shown.

a)

b)

c)

d)

e)

2. (15 points) Write accurate structures for each of the following:

a) p-nitrobenzoic acid

b) 2,6-dimethylpyridine

c) 2-(4-methoxyphenyl)ethanol

d) the HOMO of benzene (either one)

e) the product of a Birch reduction on o-diethylbenzene

3. (15 points) Compare each of the following with respect to the property indicated. Write “MOST” and “LEAST” under the compounds with the highest and lowest values.

a) reactivity towards Br2

b) amount of para substitution expected

c) SN1 reactivity

d) reactivity in a Friedel-Crafts alkylation

e) relative energy level (MOST = most stable, or lowest energy)

4. (15 points) Complete each of the following reactions by adding the missing part: either the starting compound, the necessary reagents and conditions, or the expected major product.

a)

b)

c)

d)

e)

5. (20 points) Write a synthetic sequence of reactions that could be used to prepare the following compounds, starting from benzene.

6. (10 points) Write a complete mechanism for the bromination of chlorobenzene to form
p-bromochlorobenzene. Show all steps and show all resonance forms for any intermediates involved.

7. (10 points) The heterocycle shown below has two tautomeric forms, which are readily interconverted by acid.
Identify which structures (A, B, and/or C) would be classified as aromatic.
Write all the resonance forms for B, including lone pairs.