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Chapter 11: Q.11-50f (page 350)

Question:What products would you expect from the reaction of 1-bromopropane with each of the following?

(f) Mg, then H2O

Short Answer

Expert verified

Answer

CH3CH2CH2叠谤+惭驳叠谤鈫扖贬3CH2CH2MgBr+H2翱鈫扖贬3CH2CH3Substitutionreaction

Step by step solution

01

'Step1: SN2 reaction

It is a nucleophilic substitution reaction in which an old bond is broken, and a new bond is formed. Both processes occur simultaneously. Hence, it is a single step reaction.

Two reacting species are involved in the rate-determining steps.

02

 Reaction of CH3CH2CH2Br+MgBr/H2O

CH3CH2CH2叠谤+惭驳叠谤鈫扖贬3CH2CH2MgBr+H2翱鈫扖贬3CH2CH3Substitutionreaction

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Most popular questions from this chapter

How might you prepare each of the following molecules using a nucleophilic substitution reaction at some step?

d.CH3CH2CH2CH2NH2

Question: The reactions shown below are unlikely to occur as written. Tell what is wrong with each, and predict the actual product.

b.

Which reactant in each of the following pairs is more nucleophilic? Explain.

(e) I- or Cl-

Question: (R)-2-Bromooctane undergoes racemization to give (卤)-2-bromooctane when treated with NaBr in dimethyl sulfoxide. Explain.

Propose a structure for an alkyl halide that gives only (E)-3-methyl-2-phenyl-2-pentene on E2elimination. Make sure you indicate the stereochemistry.
See all solutions

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