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6.2: Uses of Extraction

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    535980
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    There are several reasons to use extraction in the chemistry lab. It is a principal method for isolating compounds from plant materials. Extraction moves compounds from one liquid to another, so that they can be more easily manipulated or concentrated. It also enables the selective removal of components in a mixture.

    Extracting Natural Compounds

    Fruit and plant leaves are primarily composed of cellulose and water, but also contain "essential oils." a greasy mixture of compounds that capture the "essence" of the plant material's smell and taste. Orange oil is roughly 95% limonene, and due to its nonpolar structure, can be extracted from its rind into an organic solvent like hexanes or dichloromethane. The oil can then be concentrated and used to flavor or scent foods, cleaning supplies, and candles.

    Selective Removal of Components

    When conducting an experiment that synthesizes a chemical product, a reaction is often complete whenever stirring or heating is complete. Directly afterwards more steps are needed to "work-up" the reaction in some way. A work-up refers to methods aimed at isolating the product from the reaction mixture, and often begins by using a separatory funnel and extractions.

    For example, imagine that acetic acid and isopentanol have been heated in the presence of an acid catalyst for one hour in order to make isopentyl acetate, an ester that smells of bananas. After the one-hour time period, there is unfortunately not just the banana-smelling ester in the flask. The flask will also contain byproducts, leftover starting materials if the reaction is incomplete, as well as any catalysts used. In this example, there could be five compounds in the reaction flask after heating is complete.

    Chemical reaction: acetic acid plus isopentanol react in the presence of sulfuric acid to form isopentyl acetate plus water.
    Reaction scheme to produce isopentyl acetate.

    When "working up" this reaction, the resulting mixture is often poured into a separatory funnel along with some water and organic solvent. This produces two layers in the separatory funnel: an aqueous layer and an organic layer.

    After shaking this heterogeneous mixture, the compounds distribute themselves based on their solubility. Compounds that have high water solubility favor the aqueous layer while less polar compounds favor the organic layer. In this example, the acid catalyst and residual carboxylic acid or alcohol would likely be drawn into the water layer. The ester would have a greater affinity for the organic layer than the aqueous layer, causing it to be isolated from the other components in the reaction mixture.

    Diagram of extraction. Stage one: products and reactants from previous reaction floating in one liquid layer. Stage 2: new liquid layer added on top with isopentyl acetate. All other molecules remain in the bottom layer.
    Extraction using water and an organic solvent to isolate isopentyl acetate from the reaction mixture.

    Adapted from Uses of Extraction by Lisa Nichols.


    6.2: Uses of Extraction is shared under a CC BY-NC 4.0 license and was authored, remixed, and/or curated by LibreTexts.

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