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Activity 2 (Nomenclature of Carboxylic Acids)
Activity 2 (Nomenclature of Carboxylic Acids)
Carboxylic acids contain a functional group, commonly written as -CO2H or COOH (note: the acidic hydrogen is bold). The carbon atom of the acid (the carbonyl carbon) will be atom number 1 in the numbering scheme. Since it always occurs at the end(s) of the chain of carbon atoms, the number is omitted. In naming the acid, the final -e of the alkane is replaced by -oic acid (note: two words in the name). The general formula for an acid is CnH2nO2. As with several of the other functional groups discussed to this point, there are a large number of acids with common names which will be underlined.
When the -CO2H group is attached to a ring, the acid is named as a cycloalkane carboxylic acid (note the -e is retained). Di-acids occur as well. In this case, since the acid groups must be at each end of the chain, numbers are not necessary to indicate their location.
Examples naming simple acids: Compound Name methanoic acid or formic acid ethanoic acid or acetic acid propanoic acid
Line Drawing
2-methylpropanoic acid
Examples naming more complex acids: Compound Name 2-hydroxypropanoic acid or lactic acid Line Drawing
5,5-dimethyl-3-oxohexanoic acid
Acids as Substituents: In more complex molecules with higher priority functional groups, the acid is named as a carboxy- substituent. It is located by numbering the longest chain of carbons (according to the higher priority functional group) and locating the -CO2H group by this numbering scheme.
Nomenclature and examples Carboxylic acids are commonly named as indicated in the table below. Although rarely used, IUPAC-recommended names also exist. For example, butyric acid (C3H7CO2H) is, according to IUPAC guidelines, also known as butanoic acid. The carboxylate anion R-COO is usually named with the suffix -ate, so acetic acid, for example, becomes acetate ion. In IUPAC nomenclature, carboxylic acids have an -oic acid suffix (e.g., octadecanoic acid). In common nomenclature, the suffix is usually -ic acid (e.g.,stearic acid). Straight-chained, saturated carboxylic acids
IUPAC name
Chemical formula
Formic acid
Methanoic acid
HCOOH
Insect stings
Acetic acid
Ethanoic acid
CH3COOH
Vinegar
Propionic acid
Propanoic acid
CH3CH2COOH
Butyric acid
Butanoic acid
CH3(CH2)2COOH
Rancid butter
Valeric acid
Pentanoic acid
CH3(CH2)3COOH
Valerian
Caproic acid
Hexanoic acid
CH3(CH2)4COOH
Goat fat
Enanthic acid
Heptanoic acid
CH3(CH2)5COOH
Caprylic acid
Octanoic acid
CH3(CH2)6COOH
CH3(CH2)7COOH
Pelargonium
10
Capric acid
Decanoic acid
CH3(CH2)8COOH
11
Undecylic acid
Undecanoic acid
CH3(CH2)9COOH
12
Lauric acid
Dodecanoic acid
CH3(CH2)10COOH
13
Tridecylic acid
Tridecanoic acid
CH3(CH2)11COOH
14
Myristic acid
Nutmeg
15
16
Palmitic acid
Palm oil
17
margaric acid
18
Stearic acid
Octadecanoic acid
CH3(CH2)16COOH
20
Arachidic acid
Icosanoic acid
CH3(CH2)18COOH
Peanut oil
Compound class
Members
Fatty acids
medium to long-chain saturated and unsaturated monocarboxylic acids, with even number of carbons examplesdocosahexaenoic acid and eicosapentaenoic acid (nutritional supplements)
Amino acids
Keto acids
acids of biochemical significance that contain a ketone group e.g. acetoacetic acid and pyruvic acid
benzoic acid, the sodium salt of benzoic acid is used as a food preservative, salicylic acid a beta hydroxy type found in many skin care products
Dicarboxylic acids
containing two carboxyl groups examples adipic acid the monomer used to produce nylon and aldaric acid a family of sugar acids
Tricarboxylic acids
containing three carboxyl groups example citric acid found in citrus fruits and isocitric acid
containing a hydroxy group example glyceric acid, glycolic acid and lactic acid (2hydroxypropanoic acid) found in sour milk tartaric acid - found in wine
ACTIVITY: Lotion Making Ever wondered which ingredient makes up the largest percentage in lotions? Water! If you look at the ingredients list on product labels, you will notice that water is almost always listed first, meaning it is the most predominant ingredient in the product. And, it is also 'free' and readily available. So what all are you paying for? Skin care lotion is nothing more than an emulsion of oil and water. As an introduction to this wonderful and useful craft, let's make a simple lotion with just olive oil, water, and emulsifying wax. Here's what you need to make approximately a 12 fl oz batch.
Tools: - 1-cup glass measuring cup - 2-cup glass measuring cup - saucepan just large enough to fit the 1-cup measurer Ingredients: - 1/4 cup olive oil - 1 1/4 cup water - 1/4 cup emulsifying wax, available at some craft stores or online. Step 2Water Bath
Fill a small saucepan with water and set it on medium low to use as a water bath. Step 3Melt Oil and Wax
Combine the oil and e. wax into the heatproof 1-cup measurer and melt the mixture in the water bath.
Fill the 2-cup measurer with water and heat it in the microwave on high for 2 minutes or until it boils. Alternatively, boil water on the stove and pour it into the measurer. Step 5Combine
When the oil/wax mixture has melted, pour it into the water. Your lotion should now have the consistency of skim milk. Step 6Cool Slightly and Pour/Package
Let it cool slightly, stir with a spoon or chopstick and pour the lotion into a bottle while it's still warm and pourable. Otherwise, it would be hard to get the lotion into its container and you might have to use a funnel. If you're using a wide mouth jar, then this is not an issue. Step 7Shake Well
Leave the cap off to let it cool completely, but occasionally cap the lotion and give it a quick shake to help blend the mixture. Step 8Ways to Customize As is, this plain, scent-free lotion is great for babies and people with sensitive skin. But this recipe is very forgiving and you can easily vary it. Here are some suggestions: - Substitute 1/4 to 1/2 cup of the water with glycerin to make a hydrating lotion. - Substitute or combine the olive oil with other oils such as almond oil or coconut oil - Add essential oils. Use 1 - 5 drops per fl oz of lotion
ACTIVITY 2 (Nomenclature of Carboxylic Acids) Name the following structures of carboxylic acids:
1. 2. 3.
4. 5.
6. 7.
8. 9.
10.
11. 12.
13.
14.
15.
KEY TO CORRECTION:
3-ethylpentanoic acid butanedioic acid propyl pentanoate pentanoic anhydride 3-methylbutanoic acid 2-chlorobutanoic acid ethanoyl chloride benzene-1,2-dicarboxylic acid 2-methylpropanoic acid 2-hydroxybutanoic acid Sodium benzoate potassium ethanoate 2-chlorocyclopentanecarboxylic acid cyclobutanecarboxylic acid 4-amino-6-heptenoic acid