ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.)
ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.)
4th Edition
ISBN: 9781119761068
Author: Klein
Publisher: WILEY
Question
Book Icon
Chapter 1.2, Problem 1.2P
Interpretation Introduction

Interpretation:

A systematic name for the given compound has to be provided.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 1.2, Problem 1.2P , additional homework tip  1

Concept Introduction:

Nomenclature of aromatic compounds:

  • The parent is benzene ring.  Functional groups attached to it other than hydrogens are called substituents.  The name of substituent must be placed before the name of the compound as a prefix in any substituted hydrocarbon.

    Ex.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 1.2, Problem 1.2P , additional homework tip  2

  • The numerical prefixes such as di, tri, and tetra must be included in the nomenclature if more than one similar substituents are attached to the benzene ring.

    Ex.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 1.2, Problem 1.2P , additional homework tip  3

  • If different substituent groups are attached to the benzene ring, the no. one position is determined by the parent.  So the first step is to choose a suitable parent.  Then the locants are assigned in a manner that gives the lower possible number to the next substituent.

    Ex.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 1.2, Problem 1.2P , additional homework tip  4

  • For disubstituted benzenes, prefixes such as ortho, meta and para should be used.

    Ex.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 1.2, Problem 1.2P , additional homework tip  5

Blurred answer
Students have asked these similar questions
16. The proton NMR spectral information shown in this problem is for a compound with formula CioH,N. Expansions are shown for the region from 8.7 to 7.0 ppm. The normal carbon-13 spec- tral results, including DEPT-135 and DEPT-90 results, are tabulated: 7 J Normal Carbon DEPT-135 DEPT-90 19 ppm Positive No peak 122 Positive Positive cus и 124 Positive Positive 126 Positive Positive 128 No peak No peak 4° 129 Positive Positive 130 Positive Positive (144 No peak No peak 148 No peak No peak 150 Positive Positive してし
3. Propose a synthesis for the following transformation. Do not draw an arrow-pushing mechanism below, but make sure to draw the product of each proposed step (3 points). + En CN CN
Show work..don't give Ai generated solution...
Knowledge Booster
Background pattern image
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
Chemistry: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co
Text book image
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781285199030
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry In Focus
Chemistry
ISBN:9781337399692
Author:Tro, Nivaldo J.
Publisher:Cengage Learning,
Text book image
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Text book image
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning