A structure for an L-amino acid that has R configuration just like cysteine is to be given. Concept introduction: In Fischer projection formula, the amino acid molecule is represented by placing the COO- group on the top of the chiral carbon. The configuration in which the NH 3 + group is placed on right is said to be D configuration while that which has NH 3 + group on the left is called to have L configuration. Based on sequence rules, the four groups attached to the chiral carbon are arranged in the order of priorities. While viewing the molecule from the side far away from the group of lowest priority, if the arrangement of first highest priority, second highest priority and third highest priority is clockwise the molecule is said to have R configuration and if the arrangement is anti-clockwise the molecule is said to have S configuration. To give: A structure for an L-amino acid that has R configuration like cysteine.

Question

Want to see the full answer?

Answer 1

Question

Chapter 26.SE, Problem 30AP

Interpretation Introduction

Interpretation:

A structure for an L-amino acid that has R configuration just like cysteine is to be given.

Concept introduction:

In Fischer projection formula, the amino acid molecule is represented by placing the COO- group on the top of the chiral carbon. The configuration in which the NH₃⁺ group is placed on right is said to be D configuration while that which has NH₃⁺ group on the left is called to have L configuration.

Based on sequence rules, the four groups attached to the chiral carbon are arranged in the order of priorities. While viewing the molecule from the side far away from the group of lowest priority, if the arrangement of first highest priority, second highest priority and third highest priority is clockwise the molecule is said to have R configuration and if the arrangement is anti-clockwise the molecule is said to have S configuration.

To give:

A structure for an L-amino acid that has R configuration like cysteine.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Identifying electron-donating and For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects NH2 ○ donating NO2 Explanation Check withdrawing no inductive effects Resonance Effects Overall Electron-Density ○ donating O withdrawing O no resonance effects O donating O withdrawing O donating withdrawing O no inductive effects Ono resonance effects O electron-rich electron-deficient O similar to benzene O electron-rich O electron-deficient O similar to benzene olo 18 Ar 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility

Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation Check Х (Choose one) OH (Choose one) OCH3 (Choose one) OH (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center

Assign R or S to all the chiral centers in each compound drawn below porat bg 9 Br Br