Essential Organic Chemistry, Global Edition
Essential Organic Chemistry, Global Edition
3rd Edition
ISBN: 9781292089034
Author: Paula Yurkanis Bruice
Publisher: PEARSON
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 12.7, Problem 18P

(a)

Interpretation Introduction

Interpretation:

It should be determined that the product obtained from the reaction of Ethyl butanoate with LiAlH4 followed by treatment with dilute acid.

Concept introduction:

LiAlH4 is a powerful reducing agent which reacts violently with water, alcohol and reduces carbonyl, carboxylic acid and ester.

Reduction of carbonyl, carboxylic acid and ester using LiAlH4 yields corresponding alcohols.

Reduction of an ester (Methyl-2-pentenoate) by using LiAlH4 in presence of dilute acid is shown below,

Essential Organic Chemistry, Global Edition, Chapter 12.7, Problem 18P , additional homework tip  1

(b)

Interpretation Introduction

Interpretation:

It should be determined that the product obtained from the reaction of Methyl benzoate with LiAlH4 followed by treatment with dilute acid.

Concept introduction:

LiAlH4 is a powerful reducing agent which reacts violently with water, alcohol and reduces carbonyl, carboxylic acid and ester.

Reduction of carbonyl, carboxylic acid and ester using LiAlH4 yields corresponding alcohols.

Reduction of an ester (Methyl-2-pentenoate) by using LiAlH4 in presence of dilute acid is shown below,

Essential Organic Chemistry, Global Edition, Chapter 12.7, Problem 18P , additional homework tip  2

(c)

Interpretation Introduction

Interpretation:

It should be determined that the product obtained from the reaction of Pentatonic acid

with LiAlH4 followed by treatment with dilute acid.

Concept introduction:

LiAlH4 is a powerful reducing agent which reacts violently with water, alcohol and reduces carbonyl, carboxylic acid and ester.

Reduction of carbonyl, carboxylic acid and ester using LiAlH4 yields corresponding alcohols.

Reduction of a carboxylic acid (oleic acid) by using LiAlH4 in presence of dilute acid is shown below,

Essential Organic Chemistry, Global Edition, Chapter 12.7, Problem 18P , additional homework tip  3

Blurred answer
Students have asked these similar questions
What reactions and reagents can be used to make phenol from benzene if electrophilic aromatic substitution reactions are excluded and benzene is the only source of carbon?
What reaction converts benzoic acid to m-bromobenzoic acid? Alkylation Acylation Halogenation Hydrohalogenation Hydration Reduction Oxidation Nitration Sulfonation
Which could explain the stronger acidity of phenols compared to alcohols. Why? a.pi-electron delocalization b.steric effect c.hydrogen bonding d.hyperconjugation
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
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:9781305446021
Author:Lampman
Publisher:CENGAGE LEARNING - CONSIGNMENT
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
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
IR Spectroscopy; Author: Professor Dave Explains;https://www.youtube.com/watch?v=_TmevMf-Zgs;License: Standard YouTube License, CC-BY