An epimer is a type of diastereomer that differs in the stereochemistry at only one chiral center, while diastereomers differ in stereochemistry at two or more chiral centers.
The stereochemical relationship between the pair of molecules is that they are enantiomers, which are mirror images of each other but cannot be superimposed.
Epimers are a type of diastereomers that differ in the configuration of only one chiral center, while diastereomers are stereoisomers that are not mirror images of each other and differ in at least one chiral center.
Constitutional isomers have different connectivity of atoms in their structures, while stereoisomers have the same connectivity of atoms but differ in their spatial arrangement.
In organic chemistry, the R and S configurations are used to describe the spatial arrangement of atoms around a chiral center. The R configuration indicates a clockwise arrangement of substituents, while the S configuration indicates a counterclockwise arrangement.
Stereoisomers have the same connectivity of atoms but differ in their spatial arrangement, while conformational isomers have the same connectivity and spatial arrangement but differ in the rotation around single bonds.
The stereochemical relationship between the pair of molecules is that they are enantiomers, which are mirror images of each other but cannot be superimposed.
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Epimers are a type of diastereomers that differ in the configuration of only one chiral center, while diastereomers are stereoisomers that are not mirror images of each other and differ in at least one chiral center.
In stereochemistry, topicity is the stereochemical relationship between substituents and the structure to which they are attached. Depending on the relationship, such groups can be heterotopic, homotopic, enantiotopic, or diastereotopic.
Constitutional isomers have different connectivity of atoms in their structures, while stereoisomers have the same connectivity of atoms but differ in their spatial arrangement.
A committed relationship could simply be an agreement between two people. Marriage is a legally binding arrangement, licensed by the state.
Vomerine hold the prey and maxilary crush the prey.
In organic chemistry, the R and S configurations are used to describe the spatial arrangement of atoms around a chiral center. The R configuration indicates a clockwise arrangement of substituents, while the S configuration indicates a counterclockwise arrangement.
Q No. 3: (a) How MMU is used to address the physical and logical cache arrangement? Explain the difference between Least recently used and least frequently used replacement algorithm.
Stereoisomers have the same connectivity of atoms but differ in their spatial arrangement, while conformational isomers have the same connectivity and spatial arrangement but differ in the rotation around single bonds.
The difference between the first and second republic of Nigeria is the new political arrangement which is the two-party system.
Morphology focuses on the structure and formation of words, while syntax deals with the arrangement and relationships of words in sentences.