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Chapter 9: Q126P (page 391)

Predict the product for the following reaction and write a mechanism to explain how it is formed.

Short Answer

Expert verified

The production of the compound is via SN1 substitution reaction and the mechanism is given below,

Step by step solution

01

Prediction of product

The above mechanism will be a substitution reaction and SN1 reaction because the formation of carbocation will be stabilized through resonance.

02

Mechanism

The mechanism of the above reaction is given below,

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Most popular questions from this chapter

Draw the products of each of the following SN2/E2 reactions. If the products can exist as stereoisomers, show which stereoisomers are formed.

a.(3S,4S)-3-bromo-4-methylhexane + CH3O-

b.(3R,4R)-3-bromo-4-methylhexane + CH3O-

c.(3S,4R)-3-bromo-4-methylhexane + CH3O-

d.(3R,4S)-3-bromo-4-methylhexane + CH3O-

Rank the following alkyl halides from most reactive to least reactive in an SN1 reaction:

2-bromo-2-methylpentane, 2-chloro-2-methylpentane, 3-chloropentane, and 2-iodo-2-methylpentane.

What products (including stereoisomers, if applicable) are formed from the reaction of 3-bromo-3- methyl pentane:

a. with HO-?

b. with H2O?

Draw the products of the following intramolecular reactions:

Question:Draw the elimination products for each of the following E2 reactions; if the products can exist as stereoisomers, indicate which stereoisomers are obtained.

a. (2S,3S)-2-chloro-3-methylpentane + high concentration of CH3O-

b.(2S,3R)-2-chloro-3-methylpentane + high concentration of CH3O-

c.(2R,3S)-2-chloro-3-methylpentane + high concentration of CH3O-

d.(2R,3R)-2-chloro-3-methylpentane + high concentration of CH3O-

e.3-chloro-3-ethyl-2,2-dimethylpentane + high concentration of CH3CH2O-
See all solutions

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