How can you separate optical isomers?
Painfully and carefully.
Examine this previous response.
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Optical isomers can be separated using techniques such as chiral chromatography, which exploits the differences in interactions between the stationary phase and the enantiomers. Another method is crystallization, where one enantiomer forms crystals faster or slower than the other. Additionally, some chemical reactions can selectively convert one enantiomer into a different compound, leaving the other enantiomer unchanged.
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When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
- The pure #beta# and #alpha# forms of D-glucose rotate the plane of polarized light to the right by 112° and 18.7° respectively (denoted as +112 and +18.7). Are these two forms of glucose enantiomers or diastereomers?
- Which molecules are achiral and chiral?
- What is the difference between the physical properties of enantiomers and diastereomers?
- How can you determine whether a molecule is an enantiomer?
- What type of isomers are glucose and galactose?

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