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Chapter 9: Q121P (page 391)

Propose a mechanism for the following reaction:

Short Answer

Expert verified

The mechanism of the product formation is SN1 reaction via carbocation rearrangement. The mechanism is given below.

Step by step solution

01

mechanism

The above product forms through SN1 mechanism via carbocation rearrangement.

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Most popular questions from this chapter

a. Which reacts faster in an SN2 reaction?

b.Which reacts faster in an E1 reaction?

c.Which reacts faster in an SN1 reaction?

Rank the following from most reactive to least reactive in an E2reaction:

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

Draw the structure of DDE.

How will the rate of the reaction between bromomethane and hydroxide ion be affected if the following changes in concentration are made?

a. The concentration of the alkyl halide is not changed and the concentration of the nucleophile is tripled.

b. The concentration of the alkyl halide is cut in half and the concentration of the nucleophile is not changed.

c. The concentration of the alkyl halide is cut in half and the concentration of the nucleophile is doubled.
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