
Write the structure of D-erythrose?
Answer
561k+ views
Hint: Erythrose is a tetrose saccharide with the chemical formula ${C_4}{H_8}{O_4}$. It has one aldehyde group, and is part of the aldose family.
Complete answer:
Saccharide, is a group that includes sugars, starch, and cellulose commonly known as carbohydrates. The saccharides are divided into four chemical groups: monosaccharides, disaccharides, oligosaccharides, and polysaccharides. Carbohydrates are polyhydroxy aldehydes, ketones, alcohols, acids, their simple derivatives and their polymers having linkages of the acetyl type.
A Fischer projection is used to differentiate between L- and D- carbohydrates. On a Fischer projection of a monosaccharide, the penultimate carbon (alternatively, the last stereogenic carbon) of D sugars are depicted with hydrogen on the left and hydroxyl on the right. L sugars will be shown with the hydrogen on the right and the hydroxyl on the left. The D/L system (named after Latin dexter and laevus, right and left) names molecules by relating them to the molecule.
D-erythrose is the D-enantiomer of erythrose. It has a role as a plant metabolite. It is an enantiomer of a L-erythrose. Enantiomers are chiral molecules that are mirror images of one another. These molecules are non-superimposable on one another.
D-erythrose is a chiral molecule. $C-2$ and $C-3$ are stereocenters, both of which have the R configuration.
Note:
While assigning the D and L configurations of sugars, we directly look for the OH group of the bottom asymmetric carbon in the Fischer projection. If it's located on the right, we designate it with D, and if located on the left we designate it with L.
Complete answer:
Saccharide, is a group that includes sugars, starch, and cellulose commonly known as carbohydrates. The saccharides are divided into four chemical groups: monosaccharides, disaccharides, oligosaccharides, and polysaccharides. Carbohydrates are polyhydroxy aldehydes, ketones, alcohols, acids, their simple derivatives and their polymers having linkages of the acetyl type.
A Fischer projection is used to differentiate between L- and D- carbohydrates. On a Fischer projection of a monosaccharide, the penultimate carbon (alternatively, the last stereogenic carbon) of D sugars are depicted with hydrogen on the left and hydroxyl on the right. L sugars will be shown with the hydrogen on the right and the hydroxyl on the left. The D/L system (named after Latin dexter and laevus, right and left) names molecules by relating them to the molecule.
D-erythrose is the D-enantiomer of erythrose. It has a role as a plant metabolite. It is an enantiomer of a L-erythrose. Enantiomers are chiral molecules that are mirror images of one another. These molecules are non-superimposable on one another.
D-erythrose is a chiral molecule. $C-2$ and $C-3$ are stereocenters, both of which have the R configuration.
Note:
While assigning the D and L configurations of sugars, we directly look for the OH group of the bottom asymmetric carbon in the Fischer projection. If it's located on the right, we designate it with D, and if located on the left we designate it with L.
Recently Updated Pages
A man running at a speed 5 ms is viewed in the side class 12 physics CBSE

The number of solutions in x in 02pi for which sqrt class 12 maths CBSE

State and explain Hardy Weinbergs Principle class 12 biology CBSE

Write any two methods of preparation of phenol Give class 12 chemistry CBSE

Which of the following statements is wrong a Amnion class 12 biology CBSE

Differentiate between action potential and resting class 12 biology CBSE

Trending doubts
What are the major means of transport Explain each class 12 social science CBSE

Which are the Top 10 Largest Countries of the World?

Draw a labelled sketch of the human eye class 12 physics CBSE

Explain sex determination in humans with line diag class 12 biology CBSE

Explain sex determination in humans with the help of class 12 biology CBSE

Differentiate between homogeneous and heterogeneous class 12 chemistry CBSE

