ETEXT+MASTERINGCHEMISTRY STANDALONE AC
ETEXT+MASTERINGCHEMISTRY STANDALONE AC
7th Edition
ISBN: 9781269736947
Author: Bruice
Publisher: PEARSON
bartleby

Concept explainers

Question
Book Icon
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.

Blurred answer
Students have asked these similar questions
Why is the reaction of the type shown below usually done? a.To make an aldehyde or ketone less water soluble b.To make the molecule more reactive c.To protect a ketone or aldehyde carbonyl d.To increase the oxygen content e.To make the alpha hydrogens more acidic
1. Put these three common types of carbonyl compound in order of decreasing reactivity ester          amide          acid chloride    2. For the least reactive, show the interconversion to its other resonance form: How does this electron delocalisation make it stable? 3. For the most reactive, draw the mechanism of its undergoing hydrolysis (reaction with H2O): Why makes this type of carbonyl so reactive to nucleophiles?
Briefly explain why OtBu- sometimes favored over hydroxide as an elimination reagent?

Chapter 9 Solutions

ETEXT+MASTERINGCHEMISTRY STANDALONE AC

Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning