Home
Class 12
CHEMISTRY
Assertion: Except glycine, all naturally...

Assertion: Except glycine, all naturally occurring `alpha`-amino acids are optically active.
Reason : All `alpha`-amino acids occurring naturally except glycine has at least one asymmetric carbon.

A

Assertion and reason both are correct statements and reason is correct explanation for assertion.

B

Assertion and reason both are correct statements but reason is not correct explanation for assertion.

C

Assertion is correct statement but reason is wrong statement.

D

Assertion is wrong statement but reason is correct statement.

Text Solution

AI Generated Solution

The correct Answer is:
To solve the assertion and reason question, we will analyze both statements step by step. ### Step 1: Analyze the Assertion **Assertion:** Except glycine, all naturally occurring alpha-amino acids are optically active. - **Understanding Alpha-Amino Acids:** Alpha-amino acids have the general structure: \[ \text{NH}_2 - \text{CH}(\text{R}) - \text{COOH} \] where R represents a variable side chain. - **Glycine Structure:** Glycine is the simplest alpha-amino acid and has the structure: \[ \text{NH}_2 - \text{CH}_2 - \text{COOH} \] In this case, the R group is a hydrogen atom (H). - **Chirality in Amino Acids:** For a molecule to be optically active, it must have at least one chiral center (asymmetric carbon). A chiral center is a carbon atom that is bonded to four different groups. - **Conclusion on Assertion:** Since glycine has no chiral center (the carbon is bonded to two hydrogens), it is not optically active. All other naturally occurring alpha-amino acids have at least one chiral center due to their unique R groups. Therefore, the assertion is **true**. ### Step 2: Analyze the Reason **Reason:** All alpha-amino acids occurring naturally except glycine have at least one asymmetric carbon. - **Understanding Asymmetric Carbon:** An asymmetric carbon is a carbon atom that has four different substituents. In the case of alpha-amino acids (other than glycine), the carbon atom attached to the amino group (NH2) and carboxylic group (COOH) also has a distinct R group. - **Conclusion on Reason:** Since all naturally occurring alpha-amino acids (except glycine) have an R group that is different from hydrogen, they possess at least one asymmetric carbon. Thus, the reason is also **true**. ### Step 3: Determine the Relationship - The reason provided explains why the assertion is true. The presence of an asymmetric carbon in all amino acids except glycine directly leads to their optical activity. ### Final Conclusion Both the assertion and reason are true, and the reason correctly explains the assertion. ### Answer: **Both Assertion and Reason are True; Reason is the correct explanation of Assertion.** ---
Promotional Banner

Topper's Solved these Questions

  • BIOMOLECULES

    MODERN PUBLICATION|Exercise Revision Exercises (Objective Questions)(Very Short Answer Questions)|33 Videos
  • BIOMOLECULES

    MODERN PUBLICATION|Exercise Revision Exercises (Objective Questions)(Short Answer Questions)|70 Videos
  • BIOMOLECULES

    MODERN PUBLICATION|Exercise Revision Exercises (Objective Questions)(Multiple Choice Questions)(Passage Based Questions)|10 Videos
  • ALDEHYDES ,KETONES AND CARBOXYLIC ACIDS

    MODERN PUBLICATION|Exercise UNIT PRACTICE TEST|13 Videos
  • CHEMISTRY IN EVERYDAY LIFE

    MODERN PUBLICATION|Exercise UNIT PRACTICE TEST|13 Videos

Similar Questions

Explore conceptually related problems

Assertion: All naturally occuring alpha -amino acids are optically active Reason: Most naturally occuring amino acids have D-configuration.

Which of the following alpha -amino acids is not optically active?

Which amino acid has no asymmetric carbon?

Assertion (A) All naturally occurring alpha -aminoacids except glycine are optically active. Reason (R) Most naturally occurring amino acids have L-configuration.

Naturally occurring sugars and amino acids have configuratoin respectively.

Which of the following amino acid is not optically active and has achiral carbon ?