Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN: 9780618974122
Author: Andrei Straumanis
Publisher: Cengage Learning
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Chapter 9, Problem 11CTQ
Interpretation Introduction
Interpretation: The correct product needs to be identified for the given reaction.
Concept Introduction: The given reaction is an acid-catalyzed
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A common method where one alkyl halide is converted to another alkyl halide is known as Finkelstein reaction. In one example of this reaction the reaction of an alkyl chloride with potassium iodide is generally carry out in acetone to maximize the amount of alkyl iodine that this formed. Why does the solvent increase the amount of alkyl iodide. Hint: potassium idioide is soluble in acetone but potassium chloride is not.
The reaction of an amine with an alkyl halide gives an ammonium salt. The rate of this SN2 reaction is sensitive to the polarity of the solvent. Draw an energy diagram for this reaction in a nonpolar solvent and another in a polar solvent. Consider the nature of the transition state, and explain why this reaction should be sensitive to the polarity of the solvent. Predict whether it will be faster or slower in a more polar solvent.
When performing a nucleophilic substitution reaction and not knowing the structure of the starting material or product, how can you form a method to determine whether the reaction proceeds via an SN1 or SN2 mechanism?
Chapter 9 Solutions
Organic Chemistry: A Guided Inquiry
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- In an electrophilic aromatic substitution, the substitution pattern on the product is determine by the directing nature of the substituents on the ring. What controls the substitution pattern in a nucleophilic aromatic substitution reaction?arrow_forwardCan you answer both please, thank you!arrow_forwardIn an E2 reaction, what are the characteristics of a good base? How does a chemist tell a strong versus weak or bulky versus not bulky nucleophile? What is the best type of solvent for this reaction? Please define the terms.arrow_forward
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