Question

A compound with two double bonds is called a diene. The name of the structure shown is 1,4 pentadiene. Apply your knowledge of IUPAC nomenclature to draw the structure of 1,3-penadiene. $$\mathrm{H}_{2} \mathrm{C}=\mathrm{CH}-\mathrm{CH}_{2}-\mathrm{CH}=\mathrm{CH}_{2}$$

Short answer

The structure of 1,3-pentadiene, based on the IUPAC nomenclature, would have double bonds in the first and third positions in the carbon chain. The structure is: \(\mathrm{H}_{2}\mathrm{C}=\mathrm{CH}\)-\(\mathrm{CH}=\mathrm{CH}\)-\(\mathrm{CH}_{2}\).

Step-by-step solution

Understand the nomenclature for 1,4-pentadiene

The given name is 1,4-pentadiene. This means that there is a five-carbon chain (indicated by "pent") with double bonds on the first and fourth carbons. The structure is shown as: \(\mathrm{H}_{2}\mathrm{C}=\mathrm{CH}\)-\(\mathrm{CH}_{2}\)-\(\mathrm{CH}=\mathrm{CH}_{2}\)

Determine the position of the double bonds for 1,3-pentadiene

The name 1,3-pentadiene indicates that there is also a five-carbon chain, but with double bonds on the first and third carbons.

Draw the structure of 1,3-pentadiene

Based on the IUPAC nomenclature, the structure of 1,3-pentadiene should have the double bonds in the first and third positions in the carbon chain. So the structure will be: \(\mathrm{H}_{2}\mathrm{C}=\mathrm{CH}\)-\(\mathrm{CH}=\mathrm{CH}\)-\(\mathrm{CH}_{2}\)

Key concepts

Organic Chemistry and IUPAC Nomenclature

Organic chemistry is the scientific study of the structure, properties, composition, reactions, and synthesis of organic compounds that are composed of carbon atoms. Among its core principles is the standardized naming system for these compounds, known as IUPAC nomenclature. This system allows chemists to communicate complex information clearly and concisely.

The International Union of Pure and Applied Chemistry (IUPAC) established rules for naming organic chemical compounds. These rules ensure that each compound has a unique and universal name. When interpreting the name of an organic molecule, like 1,3-pentadiene, it is crucial to understand the meaning of each part: 'pent' refers to the five carbon atoms that form the main chain of the molecule, 'di' indicates the presence of two double bonds, and the numbers '1,3' denote the positions of these double bonds in the carbon chain.

Learning the IUPAC nomenclature is essential for students of organic chemistry as it lays the foundation for a shared language among scientists, allowing them to discuss intricate molecular structures with precision.

Chemical Bonding in Alkenes

Chemical bonding refers to the forces that hold atoms together in molecules. Organic molecules, such as alkenes, have specific types of bonds that define their structure and behavior. Alkenes are hydrocarbons that contain carbon-carbon double bonds (C=C), which are called olefinic bonds.

These double bonds are the defining feature of alkenes and have significant implications for their chemistry. The C=C bond consists of one sigma (σ) bond and one pi (π) bond. The σ bond is a single bond formed by the overlap of orbitals directly between the bonding atoms, providing the framework of the molecule. The π bond is formed by the side-to-side overlap of p orbitals and allows for the delocalization of electrons above and below the plane of the atoms involved.

This π bond results in restricted rotation around the double bond and creates a region of higher electron density, making alkenes more reactive than alkanes (which have only single bonds). In the context of IUPAC naming, understanding the bonding in alkenes helps explain why knowing the exact position of double bonds is crucial for describing the structure of the compound accurately.

Understanding Alkenes through 1,3-Pentadiene

Alkenes are a pivotal class of organic compounds in both nature and industry. They serve as fundamental building blocks in the creation of complex molecules and materials. When we look at the example of 1,3-pentadiene, we examine an alkene that contains two double bonds, characterized as a 'diene'.

To understand the structure of 1,3-pentadiene, it's important to identify the pattern indicated by its IUPAC name. The '1,3' tells us that the double bonds are located at the first and third carbons of the carbon chain. Thus, the first carbon (C1) and the third carbon (C3) in the main chain are involved in double bonds with their adjacent carbons.

The ability to draw the structure of alkenes based on their IUPAC names is an invaluable skill in organic chemistry, essential for students studying chemical reactions involving alkenes. Without a correct understanding of the structure, predicting the outcomes of these reactions or synthesizing new compounds would be challenging. Exploring structures like 1,3-pentadiene paves the way for grasping more complex concepts in the field.