Question

Draw Haworth and conformational structures for each of the following disaccharides: a. \(6-\mathrm{O}-\beta-D\) -glucopyranosyl- \(\beta-D\) -glucopyranose b. \(4-\mathrm{O}-\beta-D\) -galactopyranosyl- \(\alpha-D\) -glucopyranose c. \(4-\mathrm{O}-\beta-D\) -xylopyranosyl- \(\beta-L\) -arabinopyranose d. \(6-\mathrm{O}-\alpha-D\) -galactopyranosyl \(-\beta-D\) -fructofuranose

Short answer

First, understand the disaccharide structure; draw both Haworth and chair forms for accuracy.

Step-by-step solution

Understanding Disaccharide Structure

Disaccharides are composed of two monosaccharide units connected by a glycosidic bond. The naming indicates which carbons are connected and the orientation of the glycosidic linkage (alpha or beta). The exercise requires drawing the cyclic (Haworth) and chair (conformational) forms of the given disaccharides.

Identifying Monosaccharide Units

For each disaccharide, identify and write down the two monosaccharides involved. Determine which hydroxyl groups connect to form the glycosidic bond.

Drawing Haworth Projections

For each disaccharide, draw the Haworth projection by arranging the monosaccharides in their cyclic pyranose (or furanose if applicable) forms. Ensure the correct positioning of glycosidic bonds (e.g., beta means that the anomeric OH is opposite to CH2OH in D sugars).

Drawing Conformational Structures

Convert each Haworth projection into a chair conformational structure. The chair conformation is a more accurate representation of the three-dimensional structure and can illustrate the steric effects. Place substituents axially or equatorially based on the stereochemistry described in the Haworth structure.

Drawing Example a - 6-O-β-D-glucopyranosyl-β-D-glucopyranose

Identify the components: two glucose units. Draw glucose in a cyclic form for each as β-D-glucopyranose and connect the C6 of one to the C1 of the other in the β position (both OH groups are up in β form).

Drawing Example b - 4-O-β-D-galactopyranosyl-α-D-glucopyranose

Identify the components: galactose and glucose. Draw galactose in β-D-galactopyranose form and glucose as α-D-glucopyranose. Connect C4 of galactose to C1 of glucose in the α position (OH group of glucose is down).

Drawing Example c - 4-O-β-D-xylopyranosyl-β-L-arabinopyranose

Draw β-D-xylopyranose and β-L-arabinopyranose using their cyclic forms. Connect C4 of xylose to C1 of arabinose using the β configuration (OH groups point up).

Drawing Example d - 6-O-α-D-galactopyranosyl-β-D-fructofuranose

Draw α-D-galactopyranose and β-D-fructofuranose in their respective cyclic forms. Connect C6 of galactose to C2 of fructose such that galactose is in the α configuration.

Key concepts

Haworth Projection

The Haworth projection is a common way to depict the cyclic structures of monosaccharides in a more approachable two-dimensional form. It is particularly useful for visualizing the specific orientation of atoms around the ring. To draw a Haworth projection:

• Start by understanding the sugar type (aldose or ketose) and the number of carbon atoms it has.
• Form a hexagonal or pentagonal ring based on pyranose or furanose formation.
• Position the oxygen atom in the clockwise direction (usually at the top-right corner of the ring).

When glucose forms a ring, it can either be in a six-membered pyranose form or a five-membered furanose form. The different orientations of hydroxyl groups and the hydrogen atoms in the Haworth projection help distinguish the alpha and beta anomers.

• The beta form shows the hydroxyl group on the anomeric carbon (C1 for aldoses) pointing up in D-sugars.
• The alpha form has the hydroxyl group pointing down.

This type of projection is essential for understanding interactions and reactivity in biochemistry.

Conformational Structures

In addition to Haworth projections, conformational structures provide a more accurate depiction of three-dimensional sugar molecules and help understand their physical and chemical behavior. The chair conformation is the most stable and preferred form for six-membered sugar rings like pyranoses due to reduced steric hindrance. To draw a chair conformation:

• Draft a zig-zag shape resembling a chair with two parallel lines depicting the main carbon chain.
• Identify axial and equatorial positions for substituents, crucial for stereochemistry understanding.

Axial substituents point up or down directly, while equatorial substituents are angled slightly toward the plane, reducing steric clashes. Assigning groups accurately in the chair model is tied tightly to the orientation in the corresponding Haworth projection. In certain sugars, like glucopyranose, the chair conformation accurately highlights anti or gauche interactions, making it possible to gauge the molecule's stability. Understanding this structure helps in analyzing molecular behavior during chemical reactions, making the 3D structure significantly impactful in organic and stereochemical studies.

Glycosidic Bonds

Glycosidic bonds are the covalent linkages that bind monosaccharide units in disaccharides and polysaccharides. These bonds form between the hydroxyl groups of two sugar molecules, creating branching or linear chains with specific attributes based on their formation. Important characteristics of glycosidic bonds include:

• Formation can occur in alpha or beta configurations, affecting the resulting structure and linkage direction.
• Numbering the carbon atoms is crucial for identifying which carbons participate in the bond, usually denoted like 1→4 or 1→6 linkages.

For example, in 6-O-β-D-glucopyranosyl-β-D-glucopyranose, the description tells us that carbon 1 of one glucopyranose unit is bonded to carbon 6 of the second unit through a beta linkage. All these bonding patterns have significant implications on the molecule’s properties, including solubility and reactivity. These linkages also determine more complex carbohydrate formations such as cellulose, starch, or glycogen, each having unique biological roles and properties based on their glycosidic connections.

Pyranose and Furanose Forms

Sugars can adopt different ring formations called pyranose and furanose forms, which describe the ring's size. These forms are significant due to their effect on the molecule's stability and reactivity. The pyranose form features a six-membered ring, while the furanose form realizes a compact five-membered ring configuration.

• Pyranose forms result from cyclicization at the C1 for aldoses or C2 for ketoses and involves the creation of a hemiacetal or hemiketal linkage.
• Furanose forms usually involve the carbonyl group reacting with an oxygen from a hydroxyl group further away, such as C1 and C5 in glucose labeling to form a five-membered ring.

These formations ease the cyclical reaction conversion equilibrium between open-chain and ring forms, crucial for sugar reactivity and interactions. The form adopted by a particular sugar impacts its structural role in biological systems. For instance, in the case of 6-O-α-D-galactopyranosyl-β-D-fructofuranose, the galactose is in the pyranose form, and fructose is in the furanose form, demonstrating the flexibility and variety of structures even within a single disaccharide.