1. Which of the following alkyl bromides will undergo the Sn2
reaction the fastest?

2. Rank the following carbocations in order of increasing
stability (least stable to most stable)   

1	2	3

1, 3, 2
1, 2, 3
3, 2, 1
2, 1, 3
2, 3, 1

3. Of the carbocations in question 2, which ones are prone to 
rearangement?

1 and 2
1 only
2 only
2 and 3
None of them will rearange

4. What is the product of the following reaction:
 

5. What is the major product of the following reaction?









None of the Above

6. Which is the major product of the following reaction?

7. How many potential E2 elimination products can form from the
addition of NaOH to the following: (hint: remember that E2 elimination
occurs only with antiperiplanar stereochemistry) 


1
2
3
No Elimination Products are Possible

8.  Which of the following alkyl halides will react more quickly 
in the E1 reaction

9. Free radical chlorination (Cl2, hv) is not very selective.  Which
of the following compounds will give the most selective 
mono-chlorination (ie. only one product)?

10. What will not be a product of the following reaction?

All can be products