Quiz 5 Practice | Baamboozle - Baamboozle | The Most Fun Classroom Games!

0%

0 0 0

What would be the E2 product for the following reaction.

No reaction.

Give an example of a reagent that will favor Hoffman and one that will favor Zaitsev products

Hoffman = Ethoxide Zaitsev = tert-butoxide

Name the following

5-chloro-1,4dimethylcyclohex-1-ene

Draw the Sn2 product for (R)-2-bromohexane and NaCN

Check image

Challenge: What would be the product for the following?

SN1

Sn1/E1 rates increase with

Better leaving group, more stable carbocations, polar protic solvents

What does the S, N and the 1/2 stand in Sn1/SN2 reactions?

S for substitution. N for nucleophilic and 1/2 for the order of the rate of reaction.

Arrange the following constitutional isomers of C4H9Br in order of increasing reactivity towards SN2. Hint: Table 7.2

Check image

What are the rate-determining steps in E1 and Sn1 reactions?

Loss of leaving group, carbocation formation

Determine whether the following is Sn1/Sn2/E1 or E2 mechanism

E1,E2,E1