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7.4 Cis-Trans Isomerism in Alkenes

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  • Page ID
    67125
  • Objectives

    After completing this section, you should be able to

    1. discuss the formation of carbon-carbon double bonds using the concept of sp2 hybridization.
    2. describe the geometry of compounds containing carbon-carbon double bonds.
    3. compare the molecular parameters (bond lengths, strengths and angles) of a typical alkene with those of a typical alkane.
    4. explain why free rotation is not possible about a carbon-carbon double bond.
    5. explain why the lack of free rotation about a carbon-carbon double bond results in the occurrence of cis-trans isomerism in certain alkenes.
    6. decide whether or not cis-trans isomerism is possible for a given alkene, and where such isomerism is possible, draw the Kekulé structure of each isomer.

    Key Terms

    Make certain that you can define, and use in context, the key term below.

    • cis-trans stereoisomers

    Study Notes

    Your previous studies in chemistry may have prepared you to discuss the nature of a carbon-carbon double bond. If not, you should review Section 1.8 of this course before beginning the present section. It is particularly important that you make molecular models of some simple alkenes to gain insight into the geometry of these compounds.

    Geometric isomerism (also known as cis-trans isomerism or E-Z isomerism) is a form of stereoisomerism. Isomers are molecules that have the same molecular formula, but have a different arrangement of the atoms in space. That excludes any different arrangements which are simply due to the molecule rotating as a whole, or rotating about particular bonds. Where the atoms making up the various isomers are joined up in a different order, this is known as structural isomerism. Structural isomerism is not a form of stereoisomerism, and is dealt with elsewhere. In stereoisomerism, the atoms making up the isomers are joined up in the same order, but still manage to have a different spatial arrangement. Geometric isomerism is one form of stereoisomerism.

    Geometric (cis / trans) isomerism

    These isomers occur where you have restricted rotation somewhere in a molecule. At an introductory level in organic chemistry, examples usually just involve the carbon-carbon double bond - and that's what this page will concentrate on. Think about what happens in molecules where there is unrestricted rotation about carbon bonds - in other words where the carbon-carbon bonds are all single. The next diagram shows two possible configurations of 1,2-dichloroethane.

    These two models represent exactly the same molecule. You can get from one to the other just by twisting around the carbon-carbon single bond. These molecules are not isomers.  If you draw a structural formula instead of using models, you have to bear in mind the possibility of this free rotation about single bonds. You must accept that these two structures represent the same molecule:

    But what happens if you have a carbon-carbon double bond - as in 1,2-dichloroethene?

    These two molecules are not the same. The carbon-carbon double bond won't rotate and so you would have to take the models to pieces in order to convert one structure into the other one. That is a simple test for isomers. If you have to take a model to pieces to convert it into another one, then you've got isomers. If you merely have to twist it a bit, then you haven't!

    Drawing structural formulae for the last pair of models gives two possible isomers:

    1. In one, the two chlorine atoms are locked on opposite sides of the double bond. This is known as the trans isomer. (trans : from latin meaning "across" - as in transatlantic).
    2. In the other, the two chlorine atoms are locked on the same side of the double bond. This is know as the cis isomer. (cis : from latin meaning "on this side")

     

    The most likely example of geometric isomerism you will meet at an introductory level is but-2-ene. In one case, the CH3 groups are on opposite sides of the double bond, and in the other case they are on the same side.

    The importance of drawing geometric isomers properly

    It's very easy to miss geometric isomers in exams if you take short-cuts in drawing the structural formulae. For example, it is very tempting to draw but-2-ene as

    CH3CH=CHCH3

    If you write it like this, you will almost certainly miss the fact that there are geometric isomers. If there is even the slightest hint in a question that isomers might be involved, always draw compounds containing carbon-carbon double bonds showing the correct bond angles (120°) around the carbon atoms at the ends of the bond. In other words, use the format shown in the last diagrams above.

    How to recognize the possibility of geometric isomerism

    You obviously need to have restricted rotation somewhere in the molecule. Compounds containing a carbon-carbon double bond have this restricted rotation. (Other sorts of compounds may have restricted rotation as well, but we are concentrating on the case you are most likely to meet when you first come across geometric isomers.) If you have a carbon-carbon double bond, you need to think carefully about the possibility of geometric isomers.

    What needs to be attached to the carbon-carbon double bond?

    Think about this case:

    Although we've swapped the right-hand groups around, these are still the same molecule. To get from one to the other, all you would have to do is to turn the whole model over. You won't have geometric isomers if there are two groups the same on one end of the bond - in this case, the two pink groups on the left-hand end. So there must be two different groups on the left-hand carbon and two different groups on the right-hand one. The cases we've been exploring earlier are like this:

    But you could make things even more different and still have geometric isomers:

    Here, the blue and green groups are either on the same side of the bond or the opposite side. Or you could go the whole hog and make everything different. You still get geometric isomers, but by now the words cis and trans are meaningless. This is where the more sophisticated E-Z notation comes in.

     

    Summary

    To get geometric isomers you must have:

    • restricted rotation (often involving a carbon-carbon double bond for introductory purposes);
    • two different groups on the left-hand end of the bond and two different groups on the right-hand end. It doesn't matter whether the left-hand groups are the same as the right-hand ones or not.

    Exercises

    1. The reading shows the two geometric isomers of 2-butene, C4H8. There are two other alkenes with the formula C4H8. Draw their structures and determine whether they too can exist in cis and trans forms.

    Answers:

    1. 2-methylpropene    2-methylpropene does not have cis and trans forms.

       

      1-butene       1-butene does not have cis and trans forms.

    Questions

    Q7.4.1

    Which of the following can have cis/trans isomers? Draw their isomers.

    (CH3CH2)CH=CH2, (CH3CH2)2C=CHCH3, (CH3CH2)CH=CHCH3

    Q7.4.2

    Name the following compounds, with cis/trans nomenclature.

    Solutions

    S7.4.1

    The last compound in the list can be a cis/trans isomer.

    S7.4.2

    A – trans-4-methyl-2-hexene

    B – cis-2,5-dibromo-3-hexene

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