L-Isoleucine (CH₃CH₂CH(CH₃)CH(NH₂)COOH) - R or S Configuration

Is L-Isoleucine R or S?

L-Isoleucine (CH₃CH₂CH(CH₃)CH(NH₂)COOH) has 1 chiral center. Has two chiral centers (α and β carbons). The sec-butyl side chain branches at the β-carbon with both ethyl and methyl groups. Focus on the α-carbon for R/S assignment.. The configuration is S based on CIP priority rules.

FormulaCH₃CH₂CH(CH₃)CH(NH₂)COOH
NameL-Isoleucine
Number of Chiral Centers1
Configuration(s)S
DifficultyAdvanced

Chiral Center Analysis

L-Isoleucine (CH₃CH₂CH(CH₃)CH(NH₂)COOH) contains 1 chiral center. Has two chiral centers (α and β carbons). The sec-butyl side chain branches at the β-carbon with both ethyl and methyl groups. Focus on the α-carbon for R/S assignment.. Each chiral center is analyzed below using CIP (Cahn-Ingold-Prelog) priority rules to determine R or S configuration.

CIP Priority Assignment

The four substituents on the chiral center are ranked by atomic number of the directly attached atom, with ties broken by exploring outward along each branch.

R/S Configuration

With the lowest priority group (priority 4) oriented away from the viewer, the remaining three substituents trace a counterclockwise path from priority 1 to 2 to 3. This gives the S configuration.

Interactive stereochemistry explorer with guided walkthroughs and practice quizzes.

Assign R/S Configuration for L-Isoleucine Step by Step

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