EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
2nd Edition
ISBN: 9780393630817
Author: KARTY
Publisher: W.W.NORTON+CO. (CC)
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter F, Problem F.18P
Interpretation Introduction

(a)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(b)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’. If the alkyl part of the root is a cyclic alkane, the root name is cycloalkanecarboxamide.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Interpretation Introduction

(c)

Interpretation:

For the given molecule, the IUPAC is to be written.

Concept introduction:

The IUPAC name of an amide is made of two parts. The first part is based on the number of carbons in the longest continuous carbon chain of the carboxylic acid from which the amide is derived. This may include the names of any substituents present as a prefix. The final e in the name of the root alkane is replaced by the functional group suffix ‘amide’.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules and listed at the start along with the carbon number.

Blurred answer
Students have asked these similar questions
Assuming that no equilibria other than dissolution are involved, calculate the molar solubility of each of the following from its solubility product: (a) KHC4H4O6
Answer the following by equation  1. reactio of CH3MgBr with Acetone [CH3COCH3] 2. acetal formation reaction of acetaldehyde [CH3CHO] 3. preparation of ethylmethylether [C2H5OCH3]  4. the acidity of the carboxylic acid depends and affected by the substitutions on the rest of the acid molecule: draw 2 structures of acids to show the different effects on acidity by different subs
Consider the reaction sequence below to answer the following questions: 0 0 0 0 0 1. NaOEt, EtOH H3O* OEt OET 2 PhCH Br heat Ph + EtOH + CO₂ CHh B C A A. The starting material A in this reaction sequence is called a a. ẞ-keto ester b. a-carboethoxy ketone C. malonic ester d. acetoacetic ester B. Conversion of A into B is a type of reaction termed a. an acylation b. an enolation C. d. an alkylation a phenylation f reactions
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
Text book image
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Text book image
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
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
Text book image
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Text book image
Macroscale and Microscale Organic Experiments
Chemistry
ISBN:9781305577190
Author:Kenneth L. Williamson, Katherine M. Masters
Publisher:Brooks Cole
Nomenclature: Crash Course Chemistry #44; Author: CrashCourse;https://www.youtube.com/watch?v=U7wavimfNFE;License: Standard YouTube License, CC-BY