Alkanes, Alkenes vs Alkynes: Difference and Comparison

Hydrocarbons are compounds that contain carbon and hydrogen atoms. These atoms are bonded in a molecular form by different chemical bonds.

Hydrocarbons have three major types – alkanes, alkenes, and alkynes.

Key Takeaways

  1. Alkanes contain only single covalent bonds, alkenes have at least one double carbon-carbon bond, and alkynes have at least one triple carbon-carbon bond.
  2. Alkanes are saturated hydrocarbons, whereas alkenes and alkynes are unsaturated hydrocarbons.
  3. Alkanes exhibit lower reactivity than alkenes and alkynes, which readily participate in addition reactions.

Alkanes vs Alkenes vs Alkynes

Alkanes is used to describe saturated hydrocarbons that have only single bonds between carbon atoms. Alkenes are unsaturated hydrocarbons that have one or more double bonds between carbon atoms. Alkynes are also unsaturated hydrocarbons, but they have one or more triple bonds between carbon atoms.

Alkanes vs Alkenes vs Alkynes

Alkanes are also known as paraffin. Hydrogen atoms fill the valencies of the four-carbon atom.

The simplest kind of alkanes is methane, ethane, and even propane. It is widely used for various industrial processes.

While alkenes are called diene, they are unsaturated hydrocarbons because of the presence of a double bond.

They can be incorporated into all sizes of rings called cycloalkenes. The simplest kind of alkenes are ethene, propene, and others and they can be prepared in the laboratory.

On the other hand, alkynes are called trienes. Alkynes are highly combustible, and the simpler alkynes are present in a gaseous state as the compound becomes bigger, the compound can be found as liquids or even as solids.

Comparison Table

Parameters of ComparisonAlkanesAlkenesAlkynes
The bond between carbon atomsSingle bondDouble bondTriple bond
Physical propertiesColourless, low molecular weight, high boiling point, and can exist as solids, liquids and gases.Colourless, nonpolar, combustible, strong smell, exist as a gas at room temperature and has a more molecular mass.Odourless and colourless (exception – alkynes have a distinctive odour), and have high boiling and melting point with a bigger molecular structure.
Chemical properties Do not react with other chemical compounds or free radicals, are weak acids, react with electrophilic reagents, and react with oxygen and hydrogen.Less soluble in water, the longer molecular chain of alkenes has a high boiling point, and the polarity of alkanes depends on functional groups.Slightly acidic and electronegative and is combustible.
ApplicationUsed in cooking, heating, liquefied petroleum gas (LPG), natural gas, aerosol sprays, and internal combustion engines.Used in the synthesis of plastic, alcohol, fuels, vinyl chloride, ethanol, acrylic acids, glycerol ester, synthetic rubbers and production of crude oil and natural gas, and others.Used in medicines, pharmaceuticals, and other drug preparation applications, polymer, PVC and rubber synthesis. It is commonly used in industries to ripe fruits and other processes.
ExampleMethane, ethaneEthene, PropeneEthyne, propyne
Pin This Now to Remember It Later
Pin This

What is Alkane?

Alkanes are saturated hydrocarbons with hydrogen and carbon atoms arranged in a tree structure. The carbon-carbon bonds in alkanes are single.

Also Read:  Clubhouse vs Houseparty: Difference and Comparison

The IUPAC (International Union Od Pure and Applied Chemistry) definition of alkanes is “acyclic branched or unbranched hydrocarbons with a general formula of Cn H (2n+2)”.

The hybridization of alkanes is sp3. It contains four signs of bonds and is joined by carbon atoms.

The longest chain of carbon atoms linked together is called the carbon skeleton and is used to determine the size of the alkane.

Alkanes are also known as paraffin since they exhibit wax-like characteristics at certain standard ambient temperatures and pressure (SATP). Alkanes can be further classified depending upon the structure – linear branched or cyclic alkanes.

If the alkane has more than three carbon atoms, it can be arranged in various structures, forming the basis of structural isomers. Alkanes are widely used in petroleum, crude oil, and natural gas.

The different examples of methane, ethane, propane, butane, pentane, hexane, heptane, octane, and other various types.

What is Alkene?

Alkenes are a type of unsaturated hydrocarbon that has a double carbon-carbon bond. They are apolar compounds and are very reactive.

A sigma bond and a pi bond are the double bonds of carbon atoms. The bond is very strong and more stable than most single covalent bonds.

The double bond is shorter. The bond length of alkenes is 133 pm or 1.33 Å. The hybridization of alkenes is sp2.

The alkenes do not freely rotate because of an energetic cost to break. The bond angles of an alkene are about 120° from each other.

Alkenes are stable compounds but undergo several reactions like addition, hydrogenation, hydration, halogenation, hydrohalogenation, oxidation, halohydrin formation, polymerization, metal complexation, alkylation, and numerous other reactions.

Also Read:  IQ vs EQ: Difference and Comparison

Alkynes are widely used in the synthesis of plastic, alcohol, fuels, vinyl chloride, ethanol, acrylic acids, glycerol ester, synthetic rubbers, and production of crude oil and natural gas, and several other industrial processes. Example of alkenes is ethene, propene, butene, pentene, hexene, heptene, octene, nonene, and other isomers.

What is Alkyne?

Alkynes are unsaturated hydrocarbons that contain a triple carbon bond. Alkynes were known as acetylenes initially. The bond angle between the carbon atoms is 180°.

The alkynes have a rod-like structure. They are also known as olefins.

The bond length between the C-atoms is very short and 121 pm. The triple bond has a strong bond strength which is about 839 kJ/mol.

It has an sp hybridization where the s and p orbitals overlap each other and forms the three bonds.

Alkynes are named by following a suffix of “ene” after that. Alkynes can be synthesized by several processes, like cracking or dehydrohalogenation.

Alkynes are a reactive functional group and can have the following reactions like hydrogenation, halogen addition, hydration, tautomerism, cycloaddition, oxidation, or trimerization.

Alkynes are widely used in medicines, pharmaceuticals, and other drug preparation applications. Also used for polymer, PVC, and rubber synthesis.

It is commonly used in industries to ripe fruits. Examples of alkynes are propyne, butyne, pentyne, hexyne, and others.

Main Differences Between Alkanes, Alkenes, and Alkynes

  1. The chemical formula of alkanes is Cn H(2n+2), while that of alkenes is Cn H2n, while that of alkynes is Cn H(2n-2).
  2. The hybridization of an alkane is sp3, while that of alkenes is sp2, and that of alkynes is sp.
  3. Alkanes are saturated hydrocarbons, while alkanes and alkynes are unsaturated hydrocarbons.
  4. Alkanes are called paraffin, while alkanes and alkenes are called olefins.
  5. Alkanes have Van der Waals dispersion force, alkenes have weak dipole-dipole interaction, and alkynes have London dispersion forces as intermolecular forces.
  6. The bond length of alkanes is 153 pm, alkenes are 134 pm, while that of alkynes is 121 pm.
References
  1. https://pubs.rsc.org/en/content/articlehtml/2009/cc/b820048c
  2. https://aip.scitation.org/doi/abs/10.1063/1.1680347
dot 1
One request?

I’ve put so much effort writing this blog post to provide value to you. It’ll be very helpful for me, if you consider sharing it on social media or with your friends/family. SHARING IS ♥️

Emma Smith
Emma Smith

Emma Smith holds an MA degree in English from Irvine Valley College. She has been a Journalist since 2002, writing articles on the English language, Sports, and Law. Read more about me on her bio page.

5 Comments

  1. I appreciate the breakdown of alkanes, alkenes, and alkynes. It’s important to understand their differences and applications.

    • The explanations are well-researched and provide a comprehensive understanding of these hydrocarbons.

Leave a Reply

Your email address will not be published. Required fields are marked *

Want to save this article for later? Click the heart in the bottom right corner to save to your own articles box!