-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
Structure of Alkanes
Structure of Alkanes
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
Structure of Alkanes

3.1: Structure of Alkanes

31,812 Views
02:23 min
April 30, 2023

Overview

The formation of carbon-carbon bonds leading to the creation of the carbon chain is the basis of organic chemistry. August Kekulé and Archibald Scott Couper independently developed this idea of carbon chain formation.

Hydrocarbons are the simplest organic compounds composed of carbons and hydrogens. Based on the bond order between carbons, the hydrocarbons are further classified into alkanes, alkenes, and alkynes.

Alkanes are the simplest hydrocarbons with sp3 hybrid carbon atoms. These sp3 carbon atoms can form sigma bonds with sp3 orbitals of other carbon atoms or with the 1s atomic orbitals of hydrogen atoms. Since alkanes possess only single bonds between carbon atoms, they are also known as saturated hydrocarbons. The general formula of alkanes is CnH2n+2, indicating that for every "n" carbon atom, alkanes have "2n+2" hydrogen atoms.

The Lewis structure of alkanes can be simplified using the condensed structural formula. In this representation, bonds between carbon-hydrogen and carbon-carbon are omitted to simplify the structure. Further simplification is done with the help of the line-angle formula. The lines represent carbon-carbon bonds. The line end and vertex represent the carbon atoms. The hydrogens are not explicitly shown and are assumed to be present, satisfying the carbon valency.

Transcript

Compounds containing carbon and hydrogen atoms are called hydrocarbons. The simplest hydrocarbon, methane, has a tetravalent carbon atom bonded to four hydrogen atoms.

If one of the hydrogen atoms of methane is replaced with a carbon atom bonded to three hydrogen atoms, the next hydrocarbon, ethane, is formed.

Methane and ethane belong to the family of hydrocarbons called alkanes. Since alkanes contain only single covalent bonds, they are saturated hydrocarbons.

In any alkane, for example ethane, the carbon atoms are sp3 hybridized, making them tetrahedral carbons. These singly occupied hybrid orbitals overlap with the sp3 hybrid orbitals of the neighboring carbon atom to form a carbon-carbon sigma bond.

The other hybrid orbitals of carbon form sigma bonds with the 1s orbitals of each of the hydrogen atoms. The bonded atoms are at an angle of 109.5° to each other.

Examine the structures of three simple alkanes — methane, ethane, and propane. Methane, CH4, has one carbon and four hydrogen atoms; ethane, C2H6, has two carbons and six hydrogen atoms; and propane, C3H8, has three carbons and eight hydrogen atoms.

Notice that each succeeding formula has one carbon and two hydrogens — namely, a CH2 group more than the preceding formula.

In general, for every n number of carbon atoms, there will be 2n+2 hydrogen atoms. Thus, alkanes have the characteristic molecular formula: CnH2n+2.

A condensed structural formula simplifies the Lewis structure of alkanes by omitting the bonds to hydrogens or even carbon-carbon bonds.

Hydrocarbons can also be represented using line-angle or skeletal structures. The lines denote carbon-carbon bonds, with each vertex and endpoint implying a carbon atom. The hydrogens, although not explicitly shown, are assumed to be bonded to the carbons, satisfying their valency.

Key Terms and Definitions

  • Alkanes - Simplest organic compounds, composed of carbons and hydrogens.
  • Structural formula of alkanes - Represents bonds between carbon and hydrogen in alkanes.
  • Cnh2n+2 general formula - It indicates that for every n carbon atom, alkanes have 2n+2 hydrogen atoms.
  • Condensed structural formula alkanes - Simplifies Lewis structure by omitting bonds between carbon-hydrogen and carbon-carbon.
  • Saturated Hydrocarbons - Another name for Alkanes, as they possess only single bonds.

Learning Objectives

  • Define Alkanes - Explain what they are (e.g., Alkanes are simplest organic compounds).
  • Contrast structural formula vs condensed structural formula - Explain key differences (e.g., Bonds omission).
  • Explore Hydrocarbons - Describe the different types (e.g., Alkanes).
  • Explain Saturated Hydrocarbons - Describe why alkanes are considered saturated.
  • Apply Alkanes structural formula - Breakdown of its formula (e.g., c for carbon and n for number of carbon atoms).

Questions that this video will help you answer

  • What are alkanes and their general formula?
  • What does Structural formula of alkanes represent?
  • What are Saturated Hydrocarbons and why are alkanes considered saturated?

This video is also useful for

  • Students – Understand how the concept of Alkanes supports student understanding in organic chemistry.
  • Educators – Provides a clear framework to help in teaching the topic of Alkanes, their structures, and properties.
  • Researchers – Relevance for scientific study or methodology around organic compounds and hydrocarbons.
  • Chemistry Enthusiasts – Offers insights into organic compound structures, broadening interest and curiosity.

Explore More Videos

Carbon-carbon BondsOrganic ChemistryCarbon Chain FormationHydrocarbonsAlkanesAlkenesAlkynesSp3 Hybrid Carbon AtomsSigma BondsSaturated HydrocarbonsGeneral FormulaCondensed Structural FormulaLine-angle FormulaCarbon Valency

Related Videos

Structure of Alkanes

02:23

Structure of Alkanes

Alkanes and Cycloalkanes

31.8K Views

Constitutional Isomers of Alkanes

02:18

Constitutional Isomers of Alkanes

Alkanes and Cycloalkanes

21.4K Views

Nomenclature of Alkanes

02:22

Nomenclature of Alkanes

Alkanes and Cycloalkanes

25.5K Views

Physical Properties of Alkanes

02:33

Physical Properties of Alkanes

Alkanes and Cycloalkanes

13.5K Views

Newman Projections

02:06

Newman Projections

Alkanes and Cycloalkanes

19.8K Views

Conformations of Ethane and Propane

02:18

Conformations of Ethane and Propane

Alkanes and Cycloalkanes

16.4K Views

Conformations of Butane

02:20

Conformations of Butane

Alkanes and Cycloalkanes

17.1K Views

Cycloalkanes

02:28

Cycloalkanes

Alkanes and Cycloalkanes

14.9K Views

Conformations of Cycloalkanes

02:29

Conformations of Cycloalkanes

Alkanes and Cycloalkanes

13.7K Views

Conformations of Cyclohexane

02:11

Conformations of Cyclohexane

Alkanes and Cycloalkanes

14.7K Views

Chair Conformation of Cyclohexane

02:02

Chair Conformation of Cyclohexane

Alkanes and Cycloalkanes

17.4K Views

Stability of Substituted Cyclohexanes

02:30

Stability of Substituted Cyclohexanes

Alkanes and Cycloalkanes

14.4K Views

Disubstituted Cyclohexanes: <em>cis-trans</em> Isomerism

02:37

Disubstituted Cyclohexanes: <em>cis-trans</em> Isomerism

Alkanes and Cycloalkanes

13.6K Views

Combustion Energy: A Measure of Stability in Alkanes and Cycloalkanes

02:14

Combustion Energy: A Measure of Stability in Alkanes and Cycloalkanes

Alkanes and Cycloalkanes

7.5K 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