Essential Organic Chemistry (3rd Edition)
Essential Organic Chemistry (3rd Edition)
3rd Edition
ISBN: 9780321937711
Author: Paula Yurkanis Bruice
Publisher: PEARSON
Question
Book Icon
Chapter 12.7, Problem 19P

(a)

Interpretation Introduction

Interpretation:

It should be determined that the amide used to produce Benzylmethylamine on reaction with LiAlH4.

Concept introduction:

LiAH4 (Lithium aluminium hydride):

Lithium aluminium hydride is used as a reducing agent.

Lithium aluminium hydride is reduced the amide as an amine which is shown below.

Essential Organic Chemistry (3rd Edition), Chapter 12.7, Problem 19P , additional homework tip  1

(b)

Interpretation Introduction

Interpretation:

It should be determined that the amide used to produce Ethylamine on rection with LiAlH4.

Concept introduction:

LiAH4 (Lithium aluminium hydride):

Lithium aluminium hydride is used as a reducing agent.

Lithium aluminium hydride is reduced the amide as an amine which is shown below.

Essential Organic Chemistry (3rd Edition), Chapter 12.7, Problem 19P , additional homework tip  2

(c)

Interpretation Introduction

Interpretation:

It should be determined that the amide used to produce Diethylamine on rection with LiAlH4.

Concept introduction:

LiAH4 (Lithium aluminium hydride):

Lithium aluminium hydride is used as a reducing agent.

Lithium aluminium hydride is reduced the amide as an amine which is shown below.

Essential Organic Chemistry (3rd Edition), Chapter 12.7, Problem 19P , additional homework tip  3

(d)

Interpretation Introduction

Interpretation:

It should be determined that the amide used to produce Triethylamine on rection with LiAlH4.

Concept introduction:

LiAH4 (Lithium aluminium hydride):

Lithium aluminium hydride is used as a reducing agent.

Lithium aluminium hydride is reduced the amide as an amine which is shown below.

Essential Organic Chemistry (3rd Edition), Chapter 12.7, Problem 19P , additional homework tip  4

Blurred answer
Students have asked these similar questions
Q3: Describes the relationship (identical, constitutional isomers, enantiomers or diastereomers) of each pair of compounds below. ག H CH3 OH OH CH3 H3C OH OH OH ////////// C CH3 CH3 CH3 CH3 H3C CH 3 C/III..... Physics & Astronomy www.physics.northweste COOH H нош..... H 2 OH HO CH3 HOOC H CH3 CH3 CH3 Br. H H Br and H H H H
Q1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label each compound as chiral or achiral. OH HO CI Br H CI CI Br CI CI Xf x f g Br D OH Br Br H₂N R. IN Ill I -N S OMe D II H CO₂H 1/111 DuckDuckG
These are synthesis questions. You need to show how the starting material can be converted into the product(s) shown. You may use any reactions we have learned. Show all the reagents you need. Show each molecule synthesized along the way and be sure to pay attention to the regiochemistry and stereochemistry preferences for each reaction. If a racemic molecule is made along the way, you need to draw both enantiomers and label the mixture as "racemic". All of the carbon atoms of the products must come from the starting material! ? H H
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Text book image
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Text book image
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Text book image
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Text book image
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Text book image
Chemistry In Focus
Chemistry
ISBN:9781337399692
Author:Tro, Nivaldo J.
Publisher:Cengage Learning,