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Explain D and L configuration in sugars.

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The simplest carbohydrates glyceraldehyde is chosen as the standard, to assign D and L configuration to monosaccharides.

Glyceraldehyde contains one asymmetric carbon atom and exist in two enantiomeric forms

The dextro entantiomer is represented as (+) glyceraldehyde and it is referred as D-configuration i.e., D-glyceraldehyde. 

The laevo enantiomer of glyceraldehyde is represented as (-) glyceraldehyde and it corelated as Lconfiguration i.e., L-glyceraldehyde.

In Fischer projection formula, 

A monosaccharide is assigned D-configuration if the (- OH) hydroxyl group at the last chiral carbon and lies towards right hand side. 

On the other hand it is assigned L-configuration if the – OH group on the last chiral carbon atom and lies on the left hand side. 

In monosaccharides, the most oxidised carbon (i.e., -CHO) is at the top.

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