Organic Chemistry
Organic Chemistry
7th Edition
ISBN: 9780321803221
Author: Paula Y. Bruice
Publisher: Prentice Hall
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Chapter 9.2, Problem 16P

(a)

Interpretation Introduction

Interpretation:

Reason for reaction of alkyl halide with ammonia gives a low yield of primary amine but with azide ion gives a better yield has to be identified.

Concept Introduction:

  • The SN2  reaction is a type of reaction mechanism in which one bond is broken and one bond is formed i.e., in one step. SN2  is a kind of nucleophilic substitution reaction mechanism.
  • The nucleophile attacks the back side of the carbon that is attached to the halogen. Therefore it takes an inversion of configuration.
  • The configuration of the product is inverted relative to the configuration of the reactant.

(b)

Interpretation Introduction

Interpretation:

The products obtained for the given SN2  reaction has to be drawn.

Concept Introduction:

  • The SN2  reaction is a type of reaction mechanism in which one bond is broken and one bond is formed i.e., in one step. SN2  is a kind of nucleophilic substitution reaction mechanism.
  • The nucleophile attacks the back side of the carbon that is attached to the halogen. Therefore it takes an inversion of configuration.
  • The configuration of the product is inverted relative to the configuration of the reactant.

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Which or which of the statements given below is correct. I) Maleic anhydride is a carboxylic acid derivative and its reaction with water is a reduction reaction. II) Fumaric acid and maleic acid are stereoisomers of each other III) Since fumaric acid has a more stable structure than maleic acid, its boiling point is higher. A. Solo I B. I and III C. II and III D. I, II, III E. Solo III
a. What reagent(s) are needed to synthesize the enamine below. Also, draw the resonance structure(s) for the enamine. b. Predict the product of the reaction between the enamine from part a and ethyl iodide. Also explain why it forms, including any selectivities. Hint: Consider the type of reaction alkyl halides take part in and the resonance structure(s) in part a. Etl
II Provide the missing products and reagents A and B. H HO OH cat. H+ A 1. B 2. H3O+ HO Think, think, think...the aldehyde from the starting material is still here ... H

Chapter 9 Solutions

Organic Chemistry

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