Question

Draw the structural formulas for three isomers of pentane, \(\mathrm{C}_{5} \mathrm{H}_{12} .\)

Short answer

The three isomers of pentane are: 1. n-Pentane: \(\mathrm{CH}_{3}\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{3}\) 2. Isopentane (2-methylbutane): \(\mathrm{CH}_{3}\mathrm{-}\mathrm{CH\ (}\mathrm{CH}_{3})\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{3}\) 3. Neopentane (2,2-dimethylpropane): \(\mathrm{C\ (}\mathrm{CH}_{3})_{4}\)

Step-by-step solution

Draw the first isomer - n-pentane

Draw a straight chain of 5 carbon atoms bonded to each other. This straight chain is known as n-pentane, where n denotes a normal (straight) chain. \(\mathrm{CH}_{3}\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{3}\) There are no branches in this structure, and all carbon atoms are connected in a linear pattern.

Draw the second isomer - isopentane (2-methylbutane)

In this isomer, we will create a branch in the carbon skeleton by moving one carbon atom from the end of the chain to the 2nd carbon atom position in the original pentane chain. This will form a new compound, isopentane (also known as 2-methylbutane). \(\mathrm{CH}_{3}\mathrm{-}\mathrm{CH\ (}\mathrm{CH}_{3})\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{3}\) In this structure, there is a single branch on the second carbon atom, creating a new isomer.

Draw the third isomer - neopentane (2,2-dimethylpropane)

For the third isomer, create two branches by moving two carbon atoms from the end of the original pentane chain to the 2nd carbon atom position. This will form the compound neopentane, also known as 2,2-dimethylpropane. \(\mathrm{C\ (}\mathrm{CH}_{3})_{4}\) In this structure, the central carbon atom is bonded to four methyl groups (\(\mathrm{CH}_3\)), creating another unique isomer of pentane. The three isomers of pentane are: 1. n-Pentane (\(\mathrm{CH}_{3}\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{3}\)) 2. Isopentane (2-methylbutane): \(\mathrm{CH}_{3}\mathrm{-}\mathrm{CH\ (}\mathrm{CH}_{3})\mathrm{-}\mathrm{CH}_{2}\mathrm{-}\mathrm{CH}_{3}\) 3. Neopentane (2,2-dimethylpropane): \(\mathrm{C\ (}\mathrm{CH}_{3})_{4}\)

Key concepts

Structural Isomerism

In organic chemistry, structural isomerism occurs when compounds have the same molecular formula but different structural formulas. Isomers like pentane, isopentane, and neopentane illustrate this concept beautifully. Though all three share the formula \( \mathrm{C_5H_{12}} \), each has a distinct arrangement of carbon atoms. This difference in arrangement can significantly alter their physical and chemical properties. Understanding structural isomerism is crucial in predicting these properties and their applications.
This forms the basis for introducing the topic of structural diversity in organic molecules. Students often see structural isomerism as a fascinating introduction to how versatile and complex even small organic molecules can be.

Organic Chemistry

Organic chemistry is the study of carbon-containing compounds and their structures, properties, and reactions. It is a vast field, essential to understanding substances in living organisms and many synthetic materials. Organic chemistry encompasses a wide range of topics including structural isomerism, which helps chemists understand how changing the arrangement of atoms can result in different compounds.
In this area of chemistry, curiosity drives the exploration of compounds like pentane and its isomers. It not only forms the basis for creating synthetic pharmaceuticals and polymers but also helps decode biological processes. Mastering organic chemistry opens up pathways into medicinal chemistry, materials science, and biochemistry.

Alkanes

Alkanes are the simplest form of hydrocarbons, consisting solely of carbon and hydrogen atoms connected by single bonds. They are saturated hydrocarbons known for their formula \( \mathrm{C_nH_{2n+2}} \). Straight-chain alkanes, such as n-pentane, display different properties and reactivity than branched ones like isopentane and neopentane.
Understanding alkanes is foundational in organic chemistry due to their nonpolar nature and relatively inert characteristics. This makes them useful in a wide range of applications, from fuels to chemical feedstocks. Noting their role in energy production, alkanes are also central to discussions on renewable energy and environmental impact.

Chemical Structure Drawing

Chemical structure drawing is an essential skill in chemistry to visualize and understand the molecular geometry and connectivity of atoms in compounds. By using structure drawings, chemists can easily convey detailed information about the molecule's identity and perhaps predict its properties.
For instance, the structures of pentane isomers illustrate the differences that branches and molecular shapes can make. It allows chemists and students alike to grasp how subtle changes in atom placement can impact overall chemical behavior. Tools such as skeletal formulas and Lewis structures aid learners in partitioning complex compounds into understandable diagrams.