Amino Acid Configuration and Chirality

Amino Acid Configuration and Chirality

Assessment

Interactive Video

Chemistry, Biology, Science

10th Grade - University

Hard

Created by

Aiden Montgomery

FREE Resource

The video explores the stereochemistry of amino acids, focusing on R&S and D&L classifications. It explains how to determine chirality using the Cahn-Ingold-Prelog system and provides examples with alanine, phenylalanine, and cysteine. The video also covers Fischer projections and the logic behind L and R amino acids, emphasizing that cysteine is the only L amino acid with R stereochemistry.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the main difference between R&S and D&L configurations in amino acids?

R&S are used for sugars, D&L for amino acids.

R&S are for achiral molecules, D&L for chiral molecules.

R&S refer to absolute configuration, D&L to relative configuration.

R&S are used in biological contexts, D&L in chemical contexts.

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In a Fischer projection, where is the carbonyl group typically placed?

At the bottom

On the left

On the right

At the top

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the configuration of L-phenylalanine?

D

S

R

L

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which amino acid is the only L amino acid with R stereochemistry?

Glycine

Alanine

Methionine

Cysteine

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the configuration of R-alanine in a Fischer projection?

R

L

D

S

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which atom is given the highest priority when determining chirality in amino acids?

Nitrogen

Sulfur

Hydrogen

Carbon

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What determines whether an amino acid is D or L in a Fischer projection?

The position of the R group

The position of the hydrogen atom

The position of the carbonyl group

The position of the amine group

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