What does R configuration mean?

Answer 1

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:

  1. HIgher atomic number of the directly-attached atom gives higher priority
  2. Atomic number of the atom attached to the one is considered in step 1 if two substituents have the same first atom
  3. 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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Answer 2

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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Answer from HIX Tutor

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.

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