Identifying Functional Groups. Why is this necessary? Alkanes. Why is this so important? What is a functional group? 2/1/16

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1 Identifying Functional Groups The Key to Survival Why is this so important? ver and over again, you will be asked to do reactions, the details to which you will receive in lecture and via your textbook. For each reaction, reagents will be used to convert one functional group into another. If you cannot recognize what a functional group looks like, it will be impossible for you to do this process The facts that you need to remember won t mean anything And you won t be able to draw the right pieces on your molecules What is a functional group? A functional group is any collection of bonded atoms that are not simply sp 3 -sp 3 (your basic - single bond) or sp 3 -. The only family in organic chemistry that has only - and - single bonds is the alkane family and they are recognized by their LAK of functional groups (or functionality, if you will). Why is this necessary? Knowing your functional groups will make your life much easier when its time for you to identify them in a lab assignment (Infrared Spectroscopy) or when you have to remember facts, like the reaction of an alkene with water and a catalyst forms an alcohol. If you don t know what an alkene or alcohol looks like, this class is impossible. In order to identify the functional groups, you have to know what sorts of bonds are in each kind of functional group. We ll scroll through the functional groups, one at a time and compare and contrast, until you (hopefully) get used to what they look like. Just remember, organic professors are devious and sometimes the mere change from a zig-zag structure to a condensed formula can entirely confuse you! Alkanes Just for comparison s sake, let s start with something that has no functional groups. Alkanes have - single bonds and - bonds and all the carbons are sp 3 hybridized. All of the following showing below are alkanes. Those in rings are still alkanes, and are referred to as cycloalkanes but they don t have functional groups either. 1

2 Alkyl alides The alkyl halide is identified by the presence of an sp 3 -X bond in the structure. alides can be fluorine, chlorine, bromine or iodine (X=F, l, or I). Each of the following has an alkyl halide (or more specifically, alkyl bromide, alkyl chloride, alkyl iodide, if you wish): Alkenes An alkene has a = in its structure. This = might have carbon groups or hydrogen atoms attached. Each of the following are alkenes: l I Alkynes An alkyne has a triple bond between two carbon atoms in its structure. Triple bond might have carbon groups on both or perhaps one carbon group and one hydrogen atom attached (usually not drawn!). If there are two carbon groups attached, an internal alkyne. ote the linear structure, as should be the case for sp hybridized carbon atoms. Alkynes An alkyne has a triple bond between two carbon atoms in its structure. If there is one carbon group attached (and one hydrogen atom), the functional group is still called an alkyne and we fine-tune the identification by calling it a terminal alkyne : is the same as Arenes or Aromatic Rings An arene or aromatic ring, for the purpose of this introductory course, is a six-membered ring of carbon atoms, with alternating double and single bonds. It can have up to six groups attached to it. These may also be called aryl groups. The following are examples of aromatic rings: Ethers The ether is identified by the presence of -- bond in the structure. The carbon groups on the left and right side can be alkyl groups or aryl groups but they cannot be carbonyls (=). Each of the following is an ether: 2

3 Epoxides The epoxide is a specific type of ether functional group, and contains the -- bond inside a threemembered ring. Each of the following is an epoxide: The Amine The amine functional group has a nitrogen atom. The nitrogen atom can have two hydrogen atoms ( 2 ), one hydrogen atom and one carbon group (R) or two carbon groups (R 2 or RR ). The carbon groups AT be = (carbonyl). ote how each of the following has a nitrogen: 2 What is what? ne of the following is an alkyl halide, one is an ether and one is an amine. Identify which is which. What is what? ne of the following is an alkyl halide, one is an ether and one is an amine. The ether has the oxygen surrounded by carbons. The alkyl halide has the ALIDE and the amine has the nitrogen atom. ether alkyl halide amine What is what? ne of the following is an alkene, one is a terminal alkyne and one is an internal alkyne. Assign the structures to their type of functional group. What is what? ne of the following is an alkene (with a double bond) and the others have triple bonds. They are alkynes. The alkyne in the middle of the chain is the internal alkyne and the other, at the end of the chain, is the terminal alkyne. terminal alkyne alkene internal alkyne 3

4 The arbonyl ompounds There are a whole series of compounds that contain the carbonyl group, =. The classification of the functional group is dependent upon what is attached to either side of the carbon atom of the carbon group. Identify what is attached to the left and right sides of each of the following: The arbonyl ompounds The first compound has on the left and on the right. The second compound has on the left and on the right. The third compound has on the left and on the right. The Ketone (T KEYTE) The ketone functional group has a carbonyl group, =, surrounded by carbon groups on both sides. They can be alkyl groups or aromatic rings. The condensed formula for a ketone group is ()-. ote how each of the following has carbon groups on both the left and the right: The Aldehyde The aldehyde functional group has a carbonyl group, =, surrounded by a carbon group on one side and a atom on the other. The carbon group can be alkyl or aromatic. The condensed formula for an aldehyde is. ote how each of the following has a carbon group on one side and a hydrogen atom on the other: Which of the following is the aldehyde and which is the ketone? The compound on the left is the aldehyde functional group (see the on the right of the carbonyl?) and the compound on the right is the ketone (two carbon groups attached). 4

5 The arboxylic Acid The carboxylic acid functional group has a carbonyl group, =, surrounded by a carbon group on one side and a hydroxyl group,, on the other. The carbon group can be alkyl or aromatic. ote how each of the following has a carbon group on one side and an on the other: Which of the following is the aldehyde and which is the carboxylic acid? The compound on the left is the aldehyde functional group (see the on the right of the carbonyl?) and the compound on the right is the carboxylic acid (carbon on right, on left). Identify which of the following is the carboxylic acid, aldehyde and ketone: Identify what s on either side of the carbonyls: ketone aldehyde carboxylic acid The Ester (T ESTER) The ester functional group has a carbonyl group, =, surrounded by a carbon group on one side and an R group on the other. Either carbon group, attached to the = or on the atom, can be alkyl or aromatic. ote how each of the following has a carbon group on one side and an R on the other: 5

6 Identify which of the following is the ketone and which is the ester? Identify what s on either side of the carbonyls: ester ketone ote the difference between an ester and an ether. Esters have an R group attached to a carbonyl. Ethers do not. Does the following molecule contain an ester or an ether? ester ether These are the two most confused functional groups! With the R group on the =, this is an ester. What about this molecule? Does it have an ester? With the R group T on the =, there is not an ester in this molecule. otice that this has TW different functional groups, a ketone on the left and ether on the right. ketone ether 6

7 The Acid alide The acid halide functional group has a carbonyl group, =, surrounded by a carbon group on one side and an X atom on the other. X is typically a chloride or bromide. ote how each of the following has a carbon group on one side and an X on the other: l The Acid Anhydride The acid anhydride functional group has two carbonyl groups, =, surrounding a central oxygen atom, and carbon groups on the other sides of the carbonyls. The carbon groups can be the same or different. ote how each of the following has the two carbonyl groups, surrounding an oxygen atom: Which is an ester and which is an acid anhydride? ote the identifying characteristic of the double carbonyl in an acid anhydride. An ester only has one carbonyl (=). acid anhydride ester Which is an alkyl halide and which is an acid halide? Both have halides (in this case, bromides) but what makes them different? The acid halide has its chloride or bromide attached directly to a carbonyl group (=). The alkyl halide has an sp 3 hybridized carbon (alkyl group) attached to the halide. alkyl halide acid halide 7

8 The itrile The nitrile functional group has a - triple bond, and the nitrogen has a lone pair. Its commonly mistaken that the nitrogen atom has an undrawn hydrogen atom but that would be an error in both structure and thought. The condensed formula for a nitrile is. Each of the following contain a nitrile: Which is an alkyne (terminal, internal) and which is a nitrile? The nitrile has a nitrogen atom in its triple bond. The other two are alkynes. The alkyne at the end of the chain is the terminal one (with a typically unseen hydrogen now shown) while the one in the center of the chain is the internal alkyne. The itro The nitro functional group is typically drawn as one of two possible equivalent resonance forms (they look alike), containing one = and one -. The condensed formula for a nitro group is 2. ote how each of the following has a nitro group: terminal alkyne nitrile internal alkyne 2 2 So there you go You have now seen all of the functional groups commonly encountered in organic chemistry. There are others lurking out there but if you know TESE, you are in really great shape ow go try that problem set to double check yourself! 8