We can write the structure of butane (C4H10) by stringing four carbon atoms in a row,
–C–C–C–C–
and then adding enough hydrogen atoms to give each carbon atom four bonds:
The compound butane has this structure, but there is another way to put 4 carbon atoms and 10 hydrogen atoms together. Place 3 of the carbon atoms in a row and then branch the fourth one off the middle carbon atom:
Now we add enough hydrogen atoms to give each carbon four bonds.
There is a hydrocarbon that corresponds to this structure, which means that two different compounds have the same molecular formula: C4H10. The two compounds have different properties—for example, one boils at −0.5°C; the other at −11.7°C. Different compounds having the same molecular formula are called isomers. The common name for the compound with this branched chain is isobutane (Figure 12.4 “Butane and Isobutane”).
Notice that C4H10 is depicted with a bent chain in Figure 12.4 “Butane and Isobutane”. The four-carbon chain may be bent in various ways because the groups can rotate freely about the C–C bonds. However, this rotation does not change the identity of the compound. It is important to realize that bending a chain does not change the identity of the compound; all of the following represent the same compound:
The formula of isobutane shows a continuous chain of three carbon atoms only, with the fourth attached as a branch off the middle carbon atom of the continuous chain.
Unlike C4H10, the compounds methane (CH4), ethane (C2H6), and propane (C3H8) do not exist in isomeric forms because there is only one way to arrange the atoms in each formula so that each carbon atom has four bonds.
Next beyond C4H10 in the homologous series is pentane. Each compound has the same molecular formula: C5H12. (Table 12.2 “The First 10 Straight-Chain Alkanes” has a column identifying the number of possible isomers for the first 10 straight-chain alkanes.) The compound at the far left is pentane because it has all five carbon atoms in a continuous chain. The compound in the middle is isopentane; like isobutane, it has a one CH3 branch off the second carbon atom of the continuous chain. The compound at the far right, discovered after the other two, was named neopentane (from the Greek neos, meaning “new”). Although all three have the same molecular formula, they have different properties, including boiling points: pentane, 36.1°C; isopentane, 27.7°C; and neopentane, 9.5°C.
Note
A continuous (unbranched) chain of carbon atoms is often called a straight chain even though the tetrahedral arrangement about each carbon gives it a zigzag shape. Straight-chain alkanes are sometimes called normal alkanes, and their names are given the prefix n-. For example, butane is called n-butane. We will not use that prefix here because it is not a part of the system established by the International Union of Pure and Applied Chemistry.
Concept Review Exercises
-
In alkanes, can there be a two-carbon branch off the second carbon atom of a four-carbon chain? Explain.
-
A student is asked to write structural formulas for two different hydrocarbons having the molecular formula C5H12. She writes one formula with all five carbon atoms in a horizontal line and the other with four carbon atoms in a horizontal line, with a CH3 group extending down from the first carbon atom. Do these structures represent different molecules? Explain why or why not.
Answers
Key Takeaway
- Alkanes with four or more carbon atoms can exist in isomeric forms.
Exercises
-
Briefly identify the important distinctions between a straight-chain alkane and a branched-chain alkane.
-
How are butane and isobutane related? How do they differ?
-
Name each compound.
-
Write the structural formula for each compound.
- hexane
- octane
-
Indicate whether the structures in each set represent the same compound or isomers.
-
CH3CH2CH2CH3 and
-
CH3CH2CH2CH2CH3 and
-
Answers
Candela Citations
- The Basics of General, Organic, and Biological Chemistry v. 1.0. Provided by: Saylor Academy. Located at: https://saylordotorg.github.io/text_the-basics-of-general-organic-and-biological-chemistry/. License: CC BY-NC: Attribution-NonCommercial. License Terms: This text was adapted by Saylor Academy under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License without attribution as requested by the work's original creator or licensor.