Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
2nd Edition
ISBN: 9780393655551
Author: KARTY, Joel
Publisher: W. W. Norton & Company
bartleby

Concept explainers

Question
Book Icon
Chapter E, Problem E.35P
Interpretation Introduction

(a)

Interpretation:

The complete IUPAC name of the given molecule is to be written.

Concept introduction:

In an aldehyde, one side to the alkyl groups or aryl groups and on the other side to an H atom, the carbonyl carbon C=O is bonded. In the nomenclature of aldehyde, suffix “one” is added to the IUPAC name.

In the IUPAC name, the root name indicates the longest carbon chain at the end of the compound’s name. The suffix ‘al’ refers to the carbonyl group, (C=O), functional group. Any other alkyl groups, attached to the carbonyl carbon atom in an aldehyde, are treated as substituents and added in the name as a prefix. Other, lower priority, functional groups are listed as prefixes, along with numbers indicating their positions on the longest carbon chain. Prefixes, di, tri, etc., are used to denote the number of identical substituents. The substituents are written in alphabetical order when writing the IUPAC name.

Interpretation Introduction

(b)

Interpretation:

The complete IUPAC name of the given molecule is to be written.

Concept introduction:

In an aldehyde, one side to the alkyl groups or aryl groups and on the other side to an H atom, the carbonyl carbon C=O is bonded. In the nomenclature of aldehyde, suffix “one” is added to the IUPAC name.

In the IUPAC name, the root name indicates the longest carbon chain at the end of the compound’s name. The suffix ‘al’ refers to the carbonyl group, (C=O) functional group. Any other alkyl groups, attached to the carbonyl carbon atom in an aldehyde, are treated as substituents and added in the name as a prefixOther, lower priority, functional groups are listed as prefixes, along with numbers indicating their positions on the longest carbon chain. Prefixes, di, tri, etc., are used to denote the number of identical substituents. The substituents are written in alphabetical order when writing the IUPAC name.

Interpretation Introduction

(c)

Interpretation:

The complete IUPAC name of the given molecule is to be written.

Concept introduction:

In an aldehyde, one side to the alkyl groups or aryl groups and on the other side to an H atom, the carbonyl carbon C=O is bonded. In the nomenclature of aldehyde, suffix “one” is added to the IUPAC name.

In the IUPAC name, the root name indicates the longest carbon chain at the end of the compound’s name. The suffix ‘al’ refers to the carbonyl group, (C=O) functional group. Any other alkyl groups, attached to the carbonyl carbon atom in an aldehyde, are treated as substituents and added in the name as a prefix. Other, lower priority, functional groups are listed as prefixes, along with numbers indicating their positions on the longest carbon chain. Prefixes, di, tri, etc., are used to denote the number of identical substituents. The substituents are written in alphabetical order when writing the IUPAC name.

Interpretation Introduction

(d)

Interpretation:

The complete IUPAC name of the given molecule is to be written.

Concept introduction:

In an aldehyde, one side to the alkyl groups or aryl groups and on the other side to an H atom, the carbonyl carbon C=O is bonded. In the nomenclature of aldehyde, suffix “one” is added to the IUPAC name.

In the IUPAC name, the root name indicates the longest carbon chain at the end of the compound’s name. The suffix ‘al’ refers to the carbonyl (C=O) functional group. Any other alkyl groups, attached to the carbonyl carbon atom in an aldehyde, are treated as substituents and added in the name as a prefix. Other, lower priority, functional groups are listed as prefixes, along with numbers indicating their positions on the longest carbon chain. Prefixes, di, tri, etc., are used to denote the number of identical substituents. The substituents are written in alphabetical order when writing the IUPAC name.

Interpretation Introduction

(e)

Interpretation:

The complete IUPAC name of the given molecule is to be written.

Concept introduction:

In an aldehyde, one side to the alkyl groups or aryl groups and on the other side to an H atom, the carbonyl carbon C=O is bonded. In the nomenclature of aldehyde, suffix “one” is added to the IUPAC name.

In the IUPAC name, the root name indicates the longest carbon chain at the end of the compound’s name. The suffix ‘al’ refers to the carbonyl (C=O) functional group. Any other alkyl groups, attached to the carbonyl carbon atom in an aldehyde, are treated as substituents and added in the name as a prefix. Other, lower priority, functional groups are listed as prefixes, along with numbers indicating their positions on the longest carbon chain. Prefixes, di, tri, etc., are used to denote the number of identical substituents. The substituents are written in alphabetical order when writing the IUPAC name.

Blurred answer
Students have asked these similar questions
Cite three reactions in which formaldehyde behaves differently fromother aldehydes.
Provide the IUPAC name for the aldehyde molecule displayed below. H
Provide the proper IUPAC or common name for the following compound. [do not use italics in Canvas] N. H. n-methylbutanamide
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.
Recommended textbooks for you
Text book image
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,
Text book image
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
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