-1::1
Simple Hit Counter
Skip to content

Products

Solutions

×
×
Sign In

EN

EN - EnglishCN - 简体中文DE - DeutschES - EspañolKR - 한국어IT - ItalianoFR - FrançaisPT - Português do BrasilPL - PolskiHE - עִבְרִיתRU - РусскийJA - 日本語TR - TürkçeAR - العربية
Sign In Start Free Trial

RESEARCH

JoVE Journal

Peer reviewed scientific video journal

Behavior
Biochemistry
Bioengineering
Biology
Cancer Research
Chemistry
Developmental Biology
View All
JoVE Encyclopedia of Experiments

Video encyclopedia of advanced research methods

Biological Techniques
Biology
Cancer Research
Immunology
Neuroscience
Microbiology
JoVE Visualize

Visualizing science through experiment videos

EDUCATION

JoVE Core

Video textbooks for undergraduate courses

Analytical Chemistry
Anatomy and Physiology
Biology
Cell Biology
Chemistry
Civil Engineering
Electrical Engineering
View All
JoVE Science Education

Visual demonstrations of key scientific experiments

Advanced Biology
Basic Biology
Chemistry
View All
JoVE Lab Manual

Videos of experiments for undergraduate lab courses

Biology
Chemistry

BUSINESS

JoVE Business

Video textbooks for business education

Accounting
Finance
Macroeconomics
Marketing
Microeconomics

OTHERS

JoVE Quiz

Interactive video based quizzes for formative assessments

Authors

Teaching Faculty

Librarians

K12 Schools

Products

RESEARCH

JoVE Journal

Peer reviewed scientific video journal

JoVE Encyclopedia of Experiments

Video encyclopedia of advanced research methods

JoVE Visualize

Visualizing science through experiment videos

EDUCATION

JoVE Core

Video textbooks for undergraduates

JoVE Science Education

Visual demonstrations of key scientific experiments

JoVE Lab Manual

Videos of experiments for undergraduate lab courses

BUSINESS

JoVE Business

Video textbooks for business education

OTHERS

JoVE Quiz

Interactive video based quizzes for formative assessments

Solutions

Authors
Teaching Faculty
Librarians
K12 Schools

Language

English

EN

English

CN

简体中文

DE

Deutsch

ES

Español

KR

한국어

IT

Italiano

FR

Français

PT

Português do Brasil

PL

Polski

HE

עִבְרִית

RU

Русский

JA

日本語

TR

Türkçe

AR

العربية

    Menu

    JoVE Journal

    Behavior

    Biochemistry

    Bioengineering

    Biology

    Cancer Research

    Chemistry

    Developmental Biology

    Engineering

    Environment

    Genetics

    Immunology and Infection

    Medicine

    Neuroscience

    Menu

    JoVE Encyclopedia of Experiments

    Biological Techniques

    Biology

    Cancer Research

    Immunology

    Neuroscience

    Microbiology

    Menu

    JoVE Core

    Analytical Chemistry

    Anatomy and Physiology

    Biology

    Cell Biology

    Chemistry

    Civil Engineering

    Electrical Engineering

    Introduction to Psychology

    Mechanical Engineering

    Medical-Surgical Nursing

    View All

    Menu

    JoVE Science Education

    Advanced Biology

    Basic Biology

    Chemistry

    Clinical Skills

    Engineering

    Environmental Sciences

    Physics

    Psychology

    View All

    Menu

    JoVE Lab Manual

    Biology

    Chemistry

    Menu

    JoVE Business

    Accounting

    Finance

    Macroeconomics

    Marketing

    Microeconomics

Start Free Trial
Loading...
Home
JoVE Core
Organic Chemistry
Nomenclature of Aromatic Compounds with Multiple Substituents
Nomenclature of Aromatic Compounds with Multiple Substituents
JoVE Core
Organic Chemistry
A subscription to JoVE is required to view this content.  Sign in or start your free trial.
JoVE Core Organic Chemistry
Nomenclature of Aromatic Compounds with Multiple Substituents

17.3: Nomenclature of Aromatic Compounds with Multiple Substituents

9,366 Views
01:11 min
May 22, 2025

Overview

When more than one substituent is present on the benzene ring, the IUPAC nomenclature depends on the number of substituents present.

For disubstituted benzene derivatives, with two groups attached to the benzene ring, three constitutional isomers are possible. For example, consider dimethyl benzene, often called xylene, where the second methyl group can be substituted at the second, third, or fourth carbon. The relative position of the substituents is represented by prefixes ortho, meta, or para. These terms can also be represented with a single letter; ortho as ‘o’, meta as ‘m’, and para as ‘p.’ Numbers can also be used to indicate the relative position of the attached groups such as 1,2- for ortho, 1,3- for meta, and 1,4- for para. For example, the three different structures possible for dimethyl benzene are shown below.

Xylene isomers diagram with structural formulas: ortho, meta, para-dimethylbenzene.

If the two substituents are different, they are numbered and listed in alphabetical order as a prefix to the benzene.

Chemical structure of 1-Chloro-4-ethylbenzene, molecular diagram for organic chemistry learning.

When one of the substituents is part of a common name, the compound is named as a derivative of that parent compound.

Chemical structure of p-chlorobenzaldehyde molecule; aromatic compound with chlorine substituent.

Polysubstituted benzene derivatives have three or more substituents attached to the benzene ring. To name them, numbers are used to indicate the relative positions of attached groups, and the lowest possible numbers are assigned to each group, as shown below.

Benzene ring numbering for correct IUPAC nomenclature; chemical structure diagram.

Finally, the substituents are alphabetically ordered as a prefix to the benzene, as shown below.

Chemical structure diagram, 4-Chloro-1-ethyl-2-propylbenzene, illustrating molecular bonds.

When one of the substituents imparts a common name, it is given locant 1, and the molecule is named as a derivative of that parent compound, as shown below.

Chemical structure of 2,5-Dichloroaniline with molecular formula and aromatic ring diagram.

Transcript

The IUPAC nomenclature of aromatic compounds with multiple substituents depends on the number and position of the substituents.

To name the disubstituted benzene derivatives, the substituent's positions are indicated either by using the prefixes ortho, meta, and para, abbreviated as o, m, and p, respectively, or using numbers like 1,2- for ortho, 1,3-  for meta, and 1,4- for para. 

If the two substituents are different, they are numbered and listed alphabetically.

When one of the substituents imparts a common name to the compound, the compound is named as a derivative of that parent molecule.

To name polysubstituted benzene derivatives with more than two substituents, numbers are used to indicate the positions of substituents.

The substituents are given the lowest possible numbers and are listed alphabetically.

If any substituent imparts a common name, it is assigned locant one, and the compound is named as the derivative of that parent molecule.

Explore More Videos

Aromatic CompoundsNomenclatureIUPAC NomenclatureDisubstituted BenzeneConstitutional IsomersDimethyl BenzeneXyleneOrthoMetaParaPolysubstituted BenzeneSubstituentsAlphabetical OrderCommon Name

Related Videos

Aromatic Compounds: Overview

01:25

Aromatic Compounds: Overview

Aromatic Compounds

12.5K Views

Nomenclature of Aromatic Compounds with a Single Substituent

01:23

Nomenclature of Aromatic Compounds with a Single Substituent

Aromatic Compounds

9.4K Views

Nomenclature of Aromatic Compounds with Multiple Substituents

01:11

Nomenclature of Aromatic Compounds with Multiple Substituents

Aromatic Compounds

9.4K Views

Structure of Benzene: Kekulé Model

01:07

Structure of Benzene: Kekulé Model

Aromatic Compounds

10.9K Views

Structure of Benzene: Molecular Orbital Model

01:18

Structure of Benzene: Molecular Orbital Model

Aromatic Compounds

10.9K Views

Criteria for Aromaticity and the Hückel 4<em>n</em> + 2 Rule

01:20

Criteria for Aromaticity and the Hückel 4<em>n</em> + 2 Rule

Aromatic Compounds

12.1K Views

Hückel's Rule Diagram of π MOs: Frost Circle

01:08

Hückel's Rule Diagram of π MOs: Frost Circle

Aromatic Compounds

5.2K Views

Frost Circles for Different Conjugated Systems

01:18

Frost Circles for Different Conjugated Systems

Aromatic Compounds

3.3K Views

Aromatic Hydrocarbon Anions: Structural Overview

01:18

Aromatic Hydrocarbon Anions: Structural Overview

Aromatic Compounds

3.3K Views

Aromatic Hydrocarbon Cations: Structural Overview

01:18

Aromatic Hydrocarbon Cations: Structural Overview

Aromatic Compounds

3.4K Views

Five-Membered Heterocyclic Aromatic Compounds: Overview

01:13

Five-Membered Heterocyclic Aromatic Compounds: Overview

Aromatic Compounds

4.8K Views

NMR Spectroscopy of Aromatic Compounds

01:14

NMR Spectroscopy of Aromatic Compounds

Aromatic Compounds

5.5K Views

JoVE logo
Contact Us Recommend to Library
Research
  • JoVE Journal
  • JoVE Encyclopedia of Experiments
  • JoVE Visualize
Business
  • JoVE Business
Education
  • JoVE Core
  • JoVE Science Education
  • JoVE Lab Manual
  • JoVE Quizzes
Solutions
  • Authors
  • Teaching Faculty
  • Librarians
  • K12 Schools
About JoVE
  • Overview
  • Leadership
Others
  • JoVE Newsletters
  • JoVE Help Center
  • Blogs
  • Site Maps
Contact Us Recommend to Library
JoVE logo

Copyright © 2025 MyJoVE Corporation. All rights reserved

Privacy Terms of Use Policies
WeChat QR code