Optical Isomerism: Chirality of Compound in GMP?

In summary, optical isomerism, also known as chirality, occurs in certain compounds where they exist in two mirror-image forms called enantiomers. This relates to chirality as it is the property of a molecule to have a non-superimposable mirror image. GMP plays a crucial role in ensuring the quality and consistency of optically active compounds by ensuring the correct enantiomer is produced. Scientists use various analytical techniques such as polarimetry and NMR spectroscopy to determine the chirality of a compound in GMP. However, optical isomerism can cause issues in drug development and production if the desired enantiomer is not produced. There are exceptions to the rule of optical isomerism in GMP, such
  • #1
NEILS BOHR
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Homework Statement


is this compound chiral??why or why not??
http://img827.imageshack.us/i/gmp.png/


Homework Equations





The Attempt at a Solution


i don't think it is...what do u think??
 
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  • #2
Why do you think it is not chiral? Provide your reason (forum rule).
 
  • #3
If you're going to use the dash, you got to use the wedge too. Your pic doesn't make sense.
 

Related to Optical Isomerism: Chirality of Compound in GMP?

1. What is optical isomerism and how does it relate to chirality in compounds?

Optical isomerism, also known as chirality, is a phenomenon that occurs in certain compounds where they exist in two mirror-image forms that cannot be superimposed on each other. These two forms are called enantiomers and have identical chemical compositions but differ in their spatial arrangement of atoms. This relates to chirality because chirality is the property of a molecule to have a non-superimposable mirror image, and it is this property that causes optical isomerism in compounds.

2. What role does GMP play in ensuring the quality of optically active compounds?

GMP, or Good Manufacturing Practices, is a set of guidelines and regulations that ensure the consistency, quality, and safety of pharmaceutical products. In the case of optically active compounds, GMP plays a crucial role in ensuring that the correct enantiomer is produced in the desired quantity and purity. This is important as the two enantiomers of a compound can have different biological effects, and GMP ensures that only the desired enantiomer is present in the final product.

3. How do scientists determine the chirality of a compound in GMP?

There are various analytical techniques used by scientists to determine the chirality of a compound in GMP. These include polarimetry, chiral chromatography, and nuclear magnetic resonance (NMR) spectroscopy. These techniques allow scientists to analyze the spatial arrangement of atoms in a compound and determine its chirality. This is important in GMP as it ensures the correct enantiomer is produced and meets the required standards.

4. Can optical isomerism cause issues in drug development and production?

Yes, optical isomerism can cause issues in drug development and production. If a drug is intended to be a single enantiomer but is produced as a mixture of both enantiomers, it can lead to adverse effects or a lack of desired effects in patients. This is why GMP guidelines are crucial in ensuring the correct enantiomer is produced in pharmaceutical manufacturing.

5. Are there any exceptions to the rule of optical isomerism in GMP?

Yes, there are exceptions to the rule of optical isomerism in GMP. Some compounds may have more than one chiral center and can exist as multiple stereoisomers. In these cases, all the stereoisomers must be produced in the correct proportions to ensure the desired biological effects. Additionally, there are some cases where the two enantiomers of a compound may not have significantly different biological effects, and in these cases, GMP may not require the separation of enantiomers. However, this is determined on a case-by-case basis and must be carefully evaluated by scientists and regulatory bodies.

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