"

D7.1 Hydrocarbons: Why Use Lewis Structures?

Let’s start with what molecules actually look like—well, our best guess. Shown below is space-filling models of simple molecules made only of carbon and hydrogen: methane (CH4), ethane (C2H6), and propane (C3H8). These are all examples of hydrocarbons—molecules composed entirely of carbon and hydrogen atoms.

As you examine their structures, some patterns should stand out:

  • Carbon (dark atoms) tends to form four connections.
  • Hydrogen (light atoms) always forms one connection.
  • The shapes are not flat—they’re three-dimensional, with atoms arranged to minimize repulsion between electron regions.

These 3D space-filling representations give you a tangible sense of how atoms pack together. They show approximate relative sizes, angles, and how tightly atoms are bonded. But they’re also hard to sketch and annotate, especially as molecules get larger or more complex.

To make structure easier to communicate, chemists use a 2D system called Lewis structures—a symbolic shorthand for representing molecules in two dimensions. Lewis structures represent bonding and valence electrons using simple conventions:

  • Bonds are shown as lines.
  • Lone electron pairs (if any) are shown as dots.
  • Atom connectivity is drawn in flat space.

Instead of memorizing these conventions right away, we will unpack them from the 3D models. You can see, for instance, that in every structure above, carbon appears bonded to four other atoms. Lewis structures encode that information with four lines extending from each carbon.

Activity: Hydrogen and carbon connections

Look closely at the three models above. How many hydrogen atoms are bonded to each carbon? What pattern(s) do you notice about how carbon and hydrogen connect?

Write in your notebook, then left-click here for an explanation.

Methane: 4 H atoms are bonded to the C atom.

Ethane: 3 H atoms are bonded to the left C atom and 3 H atoms are bonded to the right C atom.

Propane: 3 H atoms are bonded to each of the end (terminal) C atom, and 2 H atoms are bonded to the center C atom.

Each carbon atom is bonded to four other atoms (H or C). Each hydrogen atom is bonded to one other atom.

3D space-filling models are great for visualizing how atoms occupy space and how they’re arranged. But they’re not so great for drawing on a whiteboard, annotating with electron counts, or quickly comparing two different molecules. That’s why chemists developed Lewis structures. Let’s go back to our example molecules: methane, ethane, and propane. If we translate their 3D structures into 2D Lewis structures, we notice some clear conventions:

  • Each carbon makes four lines (bonds).
  • Each hydrogen connects with one line (bond).
  • We show electrons only when they’re not in bonds.

These are not arbitrary rules—they’re patterns that emerge from the molecular models themselves. Lewis structures don’t create the structure; they reflect it.

2D Lewis structures of methane, ethane, and propane.

Activity: Hydrocarbon Lewis structures

Examine the Lewis structures for methane, ethane, and propane. How does each one encode the bonding patterns you saw in the 3D models? What is simplified or abstracted in the Lewis version?

Write in your notebook, then left-click here for an explanation.
a
Comments
Please use this form to report any inconsistencies, errors, or other things you would like to change about this page. We appreciate your comments. 🙂 (Note that we cannot answer questions via the google form. If you have a question, please post it on Piazza.)

License

Icon for the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License

Chem 109 Fall 2024 Copyright © by Chem 109 Team is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, except where otherwise noted.

Share This Book