Organic Chemistry II
	Professor Carl C. Wamser
Chem 335 - Winter Term	Exam 1

1.  (14 points)  Write complete structures for the following.

a)  (4 points)  the 1,2- and 1,4- addition products of Br2 to 2,4-hexadiene (ignore stereochemistry)

b)  (4 points)  both HOMOs of benzene

c)  (6 points)  aromatic compounds that have the following molecular formulae:

C4H5N

C5H5N

C6H7N

2.  (16 points)  Write complete structures for the following.

a)  (4 points)  both enantiomers of 1,3-dichloro-1,2-propadiene

b)  (6 points)  all the resonance forms for m-methoxybenzyl cation

c)  (6 points)  The nucleic acid adenine includes the heterocyclic structure shown below.

Is it aromatic?
For each of the five nitrogens, identify the expected hybridization of N, and indicate in which orbital the lone pair would be expected.

3.  (15 points)  Arrange the following in order with respect to the property indicated.  Write “MOST” under the compound with the highest value and “LEAST” under the compound with the lowest value.

a)  reactivity as a dienophile in a Diels-Alder reaction

b)  reactivity in nucleophilic substitution

c)  reactivity in nucleophilic substitution

d)  reactivity in nitration

e)  relative stability

4.  (15 pts)  Complete each of the following reactions by adding the expected major product. 

a)

b)

c)

d)

e)

5.  (15 points)  Predict the properties of a  CH3S-  substituent in electrophilic aromatic substitution. 

Is it activating or deactivating?      

Is it o,p- or m-directing?

Write a complete mechanism for the chlorination of the compound below to illustrate your prediction.

6.  (10 points)  Show a reaction sequence that could be used to prepare the following compound starting from benzene plus any other needed compounds or reagents.

7.  (15 points)  Chloroprene, shown below, undergoes 1,4-polymerization to form the common polymer Neoprene.  Illustrate the repeat unit of this polymer.  If there are stereochemical possibilities, show all isomers.

Illustrate both the 1,2- and 1,4- addition of HBr to chloroprene, showing the resonance forms for the expected intermediates.