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In determining the R and S configuration of a carbohydrate, the priority of substituents is determined by the atomic number of the atoms directly attached to the chiral carbon, not the total number of atoms in the substituent.

The Cahn-Ingold-Prelog (CIP) priority rules are used to assign priorities to the substituents attached to a chiral center. According to these rules, the atoms directly bonded to the chiral carbon are compared based on their atomic numbers. The higher the atomic number, the higher the priority.

In the case of CH(CH₃)₂ and CH₂CH₂Br, we compare the atoms directly attached to the chiral carbon:

For CH(CH₃)₂:

  • The first carbon (C) is directly attached to the chiral carbon and has an atomic number of 6.
  • The second carbon (C) is also directly attached to the chiral carbon and has an atomic number of 6.

For CH₂CH₂Br:

  • The first carbon (C) is directly attached to the chiral carbon and has an atomic number of 6.
  • The second carbon (C) is also directly attached to the chiral carbon and has an atomic number of 6.
  • The bromine atom (Br) is also directly attached to the chiral carbon and has an atomic number of 35.

Since bromine (Br) has a higher atomic number than carbon (C), the CH₂CH₂Br substituent has higher priority over the CH(CH₃)₂ substituent. This means that in the R and S configuration, the CH₂CH₂Br substituent would have a higher priority group than CH(CH₃)₂.

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