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Chapter 9: Q125P (page 391)

What products are formed when the following stereoisomer of 2-chloro-1,3-dimethylcyclohexane reacts with methoxide ion?

Short Answer

Expert verified

The products formed by Substitution and elimination reactions are given as below,

Step by step solution

01

Reaction procedure

The following compound undergoes reaction through elimination and substitution reaction. The formation of products and their mechanism are given below,

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Most popular questions from this chapter

Two bromoethers are obtained from the reaction of the following alkyl dihalide with methanol. Draw the structures of the ethers.

Two elimination products are obtained from the following E2 reaction

a. What are the elimination products?

b. Which is formed in greater yield? (Hint:See Problem 91.)

After a proton is removed from the OH group, which compound in each pair forms a cyclic ether more rapidly?

For each of the following reactions, (1) decide whether an E2 or an E1 occurs, and (2) draw the major elimination product:

Show how each of the following compounds can be synthesized from the given starting materials:
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