EP ORGANIC CHEMISTRY-OWL V2 ACCESS
EP ORGANIC CHEMISTRY-OWL V2 ACCESS
8th Edition
ISBN: 9781305582453
Author: Brown
Publisher: Cengage Learning
bartleby

Concept explainers

Question
Book Icon
Chapter 18.9, Problem 18.9P

(a)

Interpretation Introduction

Interpretation:

The way by which the given conversion can be done in good yield has to be shown.

Concept introduction:

Acid chlorides are most often prepared by treating a carboxylic acid with thionyl chloride.

EP ORGANIC CHEMISTRY-OWL V2 ACCESS     , Chapter 18.9, Problem 18.9P , additional homework tip  1

Gilman reagent:

It is generally represented as R2CuLi and it is a lithium and copper reagent which is used to form a new carbon-carbon bond formation in organic synthesis.

General Reaction of Gilman reagent with carbonyl compounds:

EP ORGANIC CHEMISTRY-OWL V2 ACCESS     , Chapter 18.9, Problem 18.9P , additional homework tip  2

(b)

Interpretation Introduction

Interpretation:

The way by which the given conversion can be done in good yield has to be shown.

Concept introduction:

Alkyl or aryl magnesium halides (RMgX) are known as Grignard reagent. The Grignard reaction is an organometallic chemical reaction in which the Grignard reagent act as nucleophile and attack electrophilic carbon atom that are present within polar bonds to yield a carbon-carbon bond

Synthesis of Grignard reagent is shown below,

RXAlkyl/arylhalide+MgEtherRMgXGrignardreagent

Addition of a Grignard reagent to carbon dioxide followed by protonation will produce carboxylic acid.

EP ORGANIC CHEMISTRY-OWL V2 ACCESS     , Chapter 18.9, Problem 18.9P , additional homework tip  3

Acid chlorides are most often prepared by treating a carboxylic acid with thionyl chloride.

EP ORGANIC CHEMISTRY-OWL V2 ACCESS     , Chapter 18.9, Problem 18.9P , additional homework tip  4

Blurred answer
Students have asked these similar questions
3. Write all necessary chemical reactions. Name reactants & products. TOLLEN'S "SILVER MIRROR" TEST Acetaldehyde: Acetone: Formaldehyde: Methyl Ethyl Ketone (2-Butanone): Benzaldehyde: BENEDICT'S TEST Acetaldehyde: Acetone: Formaldehyde: Methyl Ethyl Ketone (2-Butanone): Benzaldehyde:
Complete each reaction giving the product or the reactants, whichever applies.
Show how you might bring about the following conversions. For any conversion involving more than one step, show  intermediate compound

Chapter 18 Solutions

EP ORGANIC CHEMISTRY-OWL V2 ACCESS

Ch. 18.8 - The following sequence of steps is used to create...Ch. 18.9 - Prob. 18.8PCh. 18.9 - Prob. 18.9PCh. 18.10 - Prob. 18.10PCh. 18.10 - Show how to convert (R)-2-phenylpropanoic acid to...Ch. 18 - Prob. 18.12PCh. 18 - Write the IUPAC name for each compound. (a)...Ch. 18 - Prob. 18.14PCh. 18 - Prob. 18.15PCh. 18 - Propose a structural formula for compound A,...Ch. 18 - Propose a structural formula for compound B,...Ch. 18 - Propose a structural formula for each compound...Ch. 18 - Draw a structural formula for the principal...Ch. 18 - Prob. 18.20PCh. 18 - Prob. 18.21PCh. 18 - Prob. 18.22PCh. 18 - Prob. 18.23PCh. 18 - Prob. 18.24PCh. 18 - Show the product expected when the following...Ch. 18 - The reagent diisobutylaluminum hydride (DIBALH)...Ch. 18 - Prob. 18.27PCh. 18 - Prob. 18.28PCh. 18 - Prob. 18.29PCh. 18 - Nicotinic acid, more commonly named niacin, is one...Ch. 18 - Prob. 18.31PCh. 18 - Prob. 18.32PCh. 18 - Prob. 18.33PCh. 18 - Prob. 18.34PCh. 18 - Prob. 18.35PCh. 18 - Isoniazid, a drug used to treat tuberculosis, is...Ch. 18 - Prob. 18.37PCh. 18 - A step in a synthesis of PGE1 (prostaglandin E1,...Ch. 18 - Prob. 18.39PCh. 18 - Prob. 18.40PCh. 18 - Show how to synthesize 5-nonanone from...Ch. 18 - Prob. 18.42PCh. 18 - The following sequence of steps converts...Ch. 18 - Prob. 18.44PCh. 18 - Prob. 18.45PCh. 18 - Prob. 18.46PCh. 18 - Prob. 18.47PCh. 18 - Following is a retrosynthetic analysis for the...Ch. 18 - Prob. 18.50PCh. 18 - Given this retrosynthetic analysis, propose a...Ch. 18 - Prob. 18.52PCh. 18 - Prob. 18.53PCh. 18 - Prob. 18.54PCh. 18 - In Problem 7.28, we saw this step in Johnsons...Ch. 18 - Prob. 18.56PCh. 18 - Prob. 18.57PCh. 18 - Prob. 18.58PCh. 18 - Prob. 18.59PCh. 18 - Prob. 18.60PCh. 18 - Prob. 18.61PCh. 18 - Prob. 18.62PCh. 18 - Using your reaction roadmap as a guide, show how...Ch. 18 - Using your reaction roadmap as a guide, show how...Ch. 18 - Using your reaction roadmap as a guide, show how...Ch. 18 - Using your reaction roadmap as a guide, show how...Ch. 18 - Minoxidil is a molecule that causes hair growth in...Ch. 18 - Prob. 18.69PCh. 18 - Prob. 18.70PCh. 18 - Prob. 18.71P
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
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning