Question

Draw the structure of glyceryl trilaurate. When this triester is saponified, what are the products?

Short answer

The products are glycerol and sodium laurate upon saponification.

Step-by-step solution

Understand Glyceryl Trilaurate Structure

Glyceryl trilaurate is a triester derived from glycerol and lauric acid. Glycerol (or glycerine) is a three-carbon molecule with the formula \( C_3H_5(OH)_3 \). Lauric acid is a 12-carbon saturated fatty acid with the formula \( C_{12}H_{24}O_2 \). Glyceryl trilaurate is formed by esterification where each hydroxyl group of glycerol forms an ester bond with a carboxyl group of lauric acid. The structure consists of a glycerol backbone with three laurate chains.

Draw the Glyceryl Trilaurate Structure

Start by drawing the glycerol backbone: three carbons connected in a row. Attach a hydroxyl group to each carbon to represent the original glycerol structure. Now, erase the hydrogen atoms of the hydroxyl groups and connect the oxygen to the carbon atom of the lauric acid to form ester linkages. Each lauric acid chain (\( C_{11}H_{23}COO^- \)) is attached, forming three ester bonds.

Understand Saponification Reaction

Saponification is the process of breaking down an ester into an alcohol and a salt of a carboxylic acid (soap) using a strong base like NaOH. In this case, glyceryl trilaurate will react with NaOH to yield glycerol and sodium laurate (the soap).

Complete Saponification Reaction

In the presence of NaOH, the esters in the glyceryl trilaurate are hydrolyzed. Each ester bond is cleaved, and glycerol (\( C_3H_5(OH)_3 \)) is regenerated as each lauric acid becomes a carboxylate anion \(( C_{11}H_{23}COO^- )\) paired with sodium ions from NaOH, forming sodium laurate.

Key concepts

Glyceryl Trilaurate

Glyceryl trilaurate is a fascinating molecule that combines glycerol and lauric acid. This compound is classified as a triester, meaning it is formed from three ester linkages. To visualize glyceryl trilaurate, imagine a backbone made of glycerol, a simple yet essential molecule that holds three reactive sites. Each of these sites interacts with lauric acid molecules through a process called esterification.

• Building Blocks: Glycerol is a three-carbon compound with three hydroxyl (-OH) groups, one attached to each carbon atom.
• Lauric Acid: A 12-carbon fatty acid (saturated), known for its role in coconut oil.

In the structure of glyceryl trilaurate, each hydroxyl group of glycerol bonds to the carboxyl group of a lauric acid, creating three ester linkages. This unified structure is what gives glyceryl trilaurate its distinct characteristics.

Esterification

Esterification is the chemical reaction responsible for the formation of ester bonds. This process typically involves an acid and an alcohol. When the acid donates its carboxyl group and the alcohol contributes its hydroxyl group, they form an ester linkage and release water as a byproduct. In the case of glyceryl trilaurate, this means lauric acid and glycerol join through ester functional groups.

• This reaction is crucial in making various esters, including those used in flavors and fragrances.
• It is often catalyzed by acidic conditions to speed up the reaction.

The formation of glyceryl trilaurate through esterification demonstrates the union of organic compounds to form more complex molecules with beneficial properties, such as in making natural soaps.

Glycerol

Glycerol is a versatile and well-known compound in biochemistry and industry. Also referred to as glycerine, it is characterized by its structure of three carbon atoms each bonded to a hydroxyl group. This gives glycerol its identity as a triol.

• Chemical Formula: \( C_3H_5(OH)_3 \)
• Its hygroscopic nature allows it to attract and retain moisture, making it valuable in skincare products and foodstuffs.

Upon the saponification of glyceryl trilaurate, glycerol is released as one of the key products. Its ability to mix well with other compounds thanks to its hydrophilic nature makes it an essential component in many health and beauty formulations.

Lauric Acid

Lauric acid is a saturated medium-chain fatty acid commonly found in coconut oil. It is renowned for its antimicrobial properties and its role in health-related products. Structurally, it contains 12 carbon atoms proportionally balanced with hydrogen, making it a saturated fatty acid.

• Chemical Formula: \( C_{12}H_{24}O_2 \)
• As a lauric acid derivative, sodium laurate acts as a natural soap in saponification reactions.

The reaction between glyceryl trilaurate and a strong base like NaOH yields sodium laurate, significantly contributing to the soap-making process. Lauric acid's balanced structure underpins these interactions and other industrial applications where it acts as a primary ingredient.