Introductory Chemistry: An Active Learning Approach
Introductory Chemistry: An Active Learning Approach
6th Edition
ISBN: 9781305079250
Author: Mark S. Cracolice, Ed Peters
Publisher: Cengage Learning
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 21, Problem 47E
Interpretation Introduction

Interpretation:

All possible xylene isomers and their IUPAC names are to be determined.

Concept introduction:

Isomers have the same molecular formula but with different structural formula.

To write the IUPAC name of an organic compound that contain a benzene ring, the steps to follow as:

1. Number the carbon atoms present in the benzene ring such that the substituents get the lowest locant number. The carbon atoms are numbered such that the substituents get the lowest possible locant number. If two or more different substituents are present, then the substituents are given preferences according to the IUPAC rule.

2. Specify the substituent position by number the carbon atom to which the substituent is bonded.

3. If there is more substituents in the compound, then they are named according to the alphabetical order.

4: While naming the compounds two digits are separated by a comma (,) and the digit is separated from a letter by a hyphen (-).If there is more substituents, then they are named in order of alphabetical order. If the similar substituent is present more than once, then the number of substituents is indicated by prefixes di, tri, tetra, etc.

5. Generally, the base name is benzene for a benzene ring. The format to name the molecule that contains a benzene ring is as follows:

substituent number-substitutent namebenzene

Blurred answer
Students have asked these similar questions
Draw all structural and geometric isomers of butene andname them.
Draw all the structural and geometric isomers of pentene,  that have an unbranched hydrocarbon chain
Explain Monosubstituted Benzenes ?

Chapter 21 Solutions

Introductory Chemistry: An Active Learning Approach

Ch. 21 - Prob. 11ECh. 21 - Prob. 12ECh. 21 - Prob. 13ECh. 21 - Prob. 14ECh. 21 - Prob. 15ECh. 21 - Prob. 16ECh. 21 - Prob. 17ECh. 21 - Prob. 18ECh. 21 - Prob. 19ECh. 21 - Prob. 20ECh. 21 - Prob. 21ECh. 21 - Prob. 22ECh. 21 - Is the general formula of a cycloalkanes the same...Ch. 21 - Prob. 24ECh. 21 - Draw the skeleton diagram of cyclopentane.Ch. 21 - Prob. 26ECh. 21 - Prob. 27ECh. 21 - Prob. 28ECh. 21 - Prob. 29ECh. 21 - Prob. 30ECh. 21 - Prob. 31ECh. 21 - Prob. 32ECh. 21 - Prob. 33ECh. 21 - Prob. 34ECh. 21 - Prob. 35ECh. 21 - Prob. 36ECh. 21 - What is the difference in bonding and in the...Ch. 21 - Prob. 38ECh. 21 - Draw the structural formula of trichloroethene, a...Ch. 21 - Prob. 40ECh. 21 - Prob. 41ECh. 21 - Prob. 42ECh. 21 - Prob. 43ECh. 21 - Prob. 44ECh. 21 - Give the IUPAC name of the following molecule:Ch. 21 - Give the IUPAC name of the following molecule:Ch. 21 - Prob. 47ECh. 21 - Prob. 48ECh. 21 - Prob. 49ECh. 21 - Prob. 50ECh. 21 - Prob. 51ECh. 21 - Prob. 52ECh. 21 - Prob. 53ECh. 21 - Prob. 54ECh. 21 - Write an equation for the hydrogenation of...Ch. 21 - Prob. 56ECh. 21 - Prob. 57ECh. 21 - Prob. 58ECh. 21 - Prob. 59ECh. 21 - Explain why the ether with formula C2H6O is very...Ch. 21 - Prob. 61ECh. 21 - Prob. 62ECh. 21 - Prob. 63ECh. 21 - Prob. 64ECh. 21 - Prob. 65ECh. 21 - Prob. 66ECh. 21 - Prob. 67ECh. 21 - Prob. 68ECh. 21 - Prob. 69ECh. 21 - Prob. 70ECh. 21 - Prob. 71ECh. 21 - Prob. 72ECh. 21 - Prob. 73ECh. 21 - Prob. 74ECh. 21 - Prob. 75ECh. 21 - Prob. 76ECh. 21 - Prob. 77ECh. 21 - Prob. 78ECh. 21 - Prob. 79ECh. 21 - Prob. 80ECh. 21 - Prob. 81ECh. 21 - Prob. 82ECh. 21 - Prob. 83ECh. 21 - Prob. 84ECh. 21 - Prob. 85ECh. 21 - Prob. 86ECh. 21 - Prob. 87ECh. 21 - Prob. 88ECh. 21 - Prob. 89ECh. 21 - Prob. 90ECh. 21 - Prob. 91ECh. 21 - Prob. 92ECh. 21 - Prob. 93ECh. 21 - Prob. 94ECh. 21 - Distinguish precisely, and in scientific terms,...Ch. 21 - Prob. 96ECh. 21 - What is the difference in bonding and in general...Ch. 21 - Draw all isomers of C4H8.Ch. 21 - Prob. 99ECh. 21 - Prob. 100ECh. 21 - Prob. 101ECh. 21 - Prob. 102ECh. 21 - Prob. 103ECh. 21 - Prob. 104ECh. 21 - Prob. 105ECh. 21 - Prob. 106ECh. 21 - Prob. 107ECh. 21 - Prob. 21.1TCCh. 21 - Prob. 21.2TCCh. 21 - Prob. 21.3TCCh. 21 - Prob. 21.4TCCh. 21 - Prob. 21.5TCCh. 21 - Prob. 21.6TCCh. 21 - Prob. 21.7TCCh. 21 - Prob. 21.8TCCh. 21 - Prob. 21.9TCCh. 21 - Prob. 21.10TCCh. 21 - Prob. 21.11TCCh. 21 - Prob. 21.12TCCh. 21 - Prob. 1CLECh. 21 - Prob. 2CLECh. 21 - Prob. 3CLECh. 21 - Prob. 4CLECh. 21 - Prob. 5CLECh. 21 - Prob. 6CLECh. 21 - Prob. 7CLECh. 21 - Prob. 8CLECh. 21 - Prob. 9CLECh. 21 - Prob. 10CLE
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
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Text book image
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / 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
Text book image
Introductory Chemistry For Today
Chemistry
ISBN:9781285644561
Author:Seager
Publisher:Cengage
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Chapter 4 Alkanes and Cycloalkanes Lesson 2; Author: Linda Hanson;https://www.youtube.com/watch?v=AL_CM_Btef4;License: Standard YouTube License, CC-BY
Chapter 4 Alkanes and Cycloalkanes Lesson 1; Author: Linda Hanson;https://www.youtube.com/watch?v=PPIa6EHJMJw;License: Standard Youtube License