Organic Chemistry
Organic Chemistry
8th Edition
ISBN: 9781305580350
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
bartleby

Concept explainers

Question
Book Icon
Chapter 18.1, Problem 18.1P

(a)

Interpretation Introduction

Interpretation:

The structural formula for the given compound has to be drawn.

Concept introduction:

Nomenclature of amides and imides:

The acyl group bonded to a nitrogen atom is the functional group of an amide.

The naming of an amide can be done by giving the suffix –oic acid from the IUPAC name of the parent acid and adding –amide.

The location of the alkyl or aryl group attached on nitrogen atom in an amide is indicated by ‘N-‘

The indication “ N,N-di-“ is used for two identical alkyl or aryl groups on nitrogen atom

(b)

Interpretation Introduction

Interpretation:

The structural formula for the given compound has to be drawn.

Concept introduction:

Nomenclature of esters of carboxylic acids:

The acyl group bonded to -ORorOAr is the functional group of a carboxylic ester.

The naming of an ester of a carboxylic acid is done by naming alkyl or aryl group bonded to oxygen first followed by the name of the acid in which the suffix –ic acid is replaced by the suffix –ate.

(c)

Interpretation Introduction

Interpretation:

The structural formula for the given compound has to be drawn.

Concept introduction:

Nomenclature of esters of carboxylic acids:

The acyl group bonded to -ORorOAr is the functional group of a carboxylic ester.

The naming of an ester of a carboxylic acid is done by naming alkyl or aryl group bonded to oxygen first followed by the name of the acid in which the suffix –ic acid is replaced by the suffix –ate.

(d)

Interpretation Introduction

Interpretation:

The structural formula for the given compound has to be drawn.

Concept introduction:

Nomenclature of amides and imides:

The acyl group bonded to a nitrogen atom is the functional group of an amide.

The naming of an amide can be done by giving the suffix –oic acid from the IUPAC name of the parent acid and adding –amide.

The location of the alkyl or aryl group attached on nitrogen atom in an amide is indicated by ‘N-‘

The indication “ N,N-di-“ is used for two identical alkyl or aryl groups on nitrogen atom

The two acyl groups bonded to a nitrogen atom is the functional group of an imide.

(e)

Interpretation Introduction

The structural formula for the given compound has to be drawn.

Concept introduction:

Nomenclature of esters of carboxylic acids:

The acyl group bonded to -ORorOAr is the functional group of a carboxylic ester.

The naming of an ester of a carboxylic acid is done by naming alkyl or aryl group bonded to oxygen first followed by the name of the acid in which the suffix –ic acid is replaced by the suffix –ate.

(f)

Interpretation Introduction

Interpretation:

The structural formula for the given compound has to be drawn.

Concept introduction:

Nomenclature of amides and imides:

The acyl group bonded to a nitrogen atom is the functional group of an amide.

The naming of an amide can be done by giving the suffix –oic acid from the IUPAC name of the parent acid and adding –amide.

The location of the alkyl or aryl group attached on nitrogen atom in an amide is indicated by ‘N-‘

The indication “ N,N-di-“ is used for two identical alkyl or aryl groups on nitrogen atom

Blurred answer
Students have asked these similar questions
What carboxylic acid and amine are needed to synthesize the pain reliever phenacetin? Phenacetin was once a component of the over-the-counter pain reliever APC (aspirin, phenacetin, caffeine), but it is no longer used because of its kidney toxicity.
Q1. How are the alkaloids classified? Q2. Give any four biological sources of quinine? Give the isolation and extraction of quinine. Q3. Give the synthesis of capsaicin from vanillin.
Explain this difference in potency and speed of onset by pointing out the main differences in functional groups between morphine and heroin.

Chapter 18 Solutions

Organic Chemistry

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
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:9781305446021
Author:Lampman
Publisher:CENGAGE LEARNING - CONSIGNMENT
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
Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning