α-D-(+)-glucose and β-D-(+)-glucose are[AIEEE 2008]a)epimer...
The carbon atom that generates the new chiral centre ( C-1 ) is called the anomeric carbon. Anomers are special cases — they are epimers that differ in configuration only at the anomeric carbon. For example, α-D-glucose and β-D-glucose are anomers.
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α-D-(+)-glucose and β-D-(+)-glucose are[AIEEE 2008]a)epimer...
Understanding Anomers
Anomers are a specific type of isomeric form related to carbohydrates, particularly sugars. The terms and relationships involved with glucose, especially the forms mentioned, can be clarified as follows:
Definition of Anomers
- Anomers are a subtype of epimers, differing at a single stereocenter, specifically the anomeric carbon (C1 in glucose).
- They arise during the cyclic formation of sugars when the carbonyl group (aldehyde or ketone) reacts with a hydroxyl group.
Alpha and Beta Forms of Glucose
- α-D-(+)-glucose has the hydroxyl group (-OH) on carbon 1 (the anomeric carbon) positioned below the plane of the ring.
- β-D-(+)-glucose has the -OH group on carbon 1 positioned above the plane of the ring.
- This difference in the orientation of the -OH group at the anomeric carbon differentiates the two forms.
Relation to Other Isomer Types
- Epimers: These are sugars that differ at any one stereogenic center, not just the anomeric carbon.
- Enantiomers: These are non-superimposable mirror images of each other, which is not the case here.
- Conformers: These are different spatial arrangements of the same molecule due to rotation around single bonds.
Conclusion
Since α-D-(+)-glucose and β-D-(+)-glucose differ solely at the anomeric carbon, they are classified as anomers. Understanding these relationships is vital in carbohydrate chemistry, particularly in biochemistry where glucose plays a crucial role.