What does R configuration mean?
It is a stereochemical label to indicate the relative spatial orientation of each atom in a molecule with a non-superimposable mirror image.
R indicates that a clockwise circular arrow that goes from higher priority to lower priority crosses over the lowest priority substituent and that lowest-priority substituent is in the back.
The R and S stereoisomers are non-superimposable mirror images, which means if you reflect them on a mirror plane, they do not become the exact same molecule when you overlay them.
When you label a molecule as R or S, you consider the priorities of each substituent on the chiral carbon (connected to four different functional groups).
Let's take this chiral amino acid for example:
Some general ways you could determine the priorities are:
- HIgher atomic number of the directly-attached atom gives higher priority
- Atomic number of the atom attached to the one is considered in step 1 if two substituents have the same first atom
- Higher number of same-atom branches determines greater priority if the overall substituents are too similar (e.g. isopropyl has higher priority than ethyl)
With (R)-alanine:
#"NH"_2# has priority 1 due to highest atomic number for#"N"# .#"COOH"# has priority 2 due to the higher atomic number of#"O"# vs.#"H"# in#"CH"_3# #"CH"_3# has priority 3 as a result.#"H"# has priority 4.Now, if you draw a circular arrow starting at
#"NH"_2# , going to#"COOH"# , crossing over#"H"# since it is in the back, and to#"CH"_3# , then you would have gone clockwise.Since the lowest priority atom is in the back, the clockwise arrow corresponds to the R configuration.
If you had started from the same R configuration but oriented
#"H"# in the front and#"CH"_3# in the back, it would have been S configuration. Let's call this S configuration A, where you just nudge two substituents to flip them from front/back to back/front.If you reflect the same R configuration over a mirror plane, keeping the orientations of
#"H"# in the back and#"CH"_3# in the front after the flip, the configuration is also S. Let's call this S configuration B, where you've actually done a reflection.If you start from S configuration B, and flipped it over a vertical axis (literally rotating
#180^o# in space), you would get S configuration A.
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The R configuration is a way to describe the spatial arrangement of atoms around a chiral center in a molecule. It indicates the orientation of the substituent groups relative to each other based on the Cahn-Ingold-Prelog priority rules. In an R configuration, the highest priority substituent is positioned on the right side of the chiral center when viewed in a specific orientation.
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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.
- If a pure R isomer has a specific rotation of –142.0°, and a sample contains 77.0% of the R isomer and 23.0% of its enantiomer, what is the observed specific rotation of the mixture?
- What does achiral mean?
- Does CH3Cl have a plane of symmetry?
- Which alkenes will result in a meso-form when the alkenes below reacts with molecular bromide (#Br_2#) cold/dark?
- How does a chiral molecule differ from an achiral molecule?
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