What are the threo and erythro isomers?
Erythro Isomers: In erythro isomers, the two identical substituents are on the same side. Threo isomers: In threo isomers, the two identical substituents are on the opposite sides. In the structure (I), the two hydroxyl groups are on the same side.
What are threo and erythro diastereomers?
Erythro and Threo Diastereomers A Diastereomer is called erythro if its Fischer projection shows similar groups on the same side of the molecule. It is called threo if similar groups are on the opposite sides of the Fischers projection.
What are erythro and threo compounds?
Erythro and threo are two configurations in which molecules are written when the molecules have a chiral carbon atom. Erythro is the configuration when the same groups are on the same side of the carbon atom and Threo is the configuration when the same groups are on the opposite side of the carbon atom.
What are Threo enantiomers?
What we see is that when two common substitutes, in this case the H and OH groups, of the stereogenic centers are on the same side, we have the sugar erythrose and when they are on opposite sides, it is the threose. Threose and erythrose exist in two enantiomeric forms which are designated as D and L enantiomers.
What does Threo mean in chemistry?
Compounds having two different chiral or assymetric carbon atoms are named by using prefix- erythro or threo. When two same groups are on the same side of chiral carbon atom in fischer Projection formula then it is ‘ erythrose ‘.
What are threo and erythro isomers give examples?
When two similar groups at non-identical chiral carbons are on the same side of the vertical line of the Fischer projection, the isomer is called erythro isomer, if the groups are on opposite sides, the isomers are called threo isomers.
What are erythro and threo isomers give examples?
Erythro / threo In the case of saccharides, when drawn in the Fischer projection the erythro isomer has two identical substituents on the same side and the threo isomer has them on opposite sides. When drawn as a zig-zag chain, the erythro isomer has two identical substituents on different sides of the plane (anti).
Which of the following is Threo isomer?
The prefixes erythro and threo are used for distinguishing a pair of enantriomers containing two chiral carbon atoms when two of the atoms or groups on each chiral carbon atom are the two identical groups are on the same side of the Fischer projection formula, is called the erythro isomer while the isomer, in which the …
Why is erythro isomer more stable than threo isomer?
The meso-form is usually thought to be more thermodynamically stable than (&)-pairs, and erythro-isomers are likely to be more stable than threo-isomers for substituted ethane derivatives except in those cases where strong intramolecular bonding is possib1e. 6 These results are presum- ably due to hydrogen bonding.
What is the difference between erythro and threo isomers?
Each pair of threo is a diastereomer of each pair of erythro isomers. The terms erythro and threo are generally used only with molecules that do not have symmetric ends. Enantiomers have identical chemical and physical properties, except theri optical rotation.
Is threo a diastereomer of erythro?
Each pair of threo is a diastereomer of each pair of erythro isomers. The terms erythro and threo are generally used only with molecules that do not have symmetric ends.
What is the erythro/threo configuration?
Erythro or threo configurations can also be evident in sawhorse projections. If the two identical groups on both chiral centers can be eclipsed, then we have the erythro configuration: However, some uncertainty arose when the erythro/threo nomenclature was applied to systems with only one common substituent on the two neighboring chiral centers.
What are the enantiomers of threo-2-3-dihydroxybutanoic acid?
For example, hydroxylation of trans-crotonic acid gives two enantiomers of the threo-2,3-dihydroxybutanoic acid whereas the same reaction with cis-crotonic acid gives the erythro enantiomers. Each pair of threo is a diastereomer of each pair of erythro isomers.