Assertion (A): All naturally occurring \(\alpha\)-amino acids except glycine are optically active. Reason (R): Most naturally occurring amino acids have L-configuration.
Assertion (A) is false, but Reason (R) is true.
Step 1: Understanding optical activity of amino acids. All naturally occurring \(\alpha\)-amino acids, except for glycine, are optically active because they contain a chiral carbon atom (except glycine, which has two hydrogen atoms on the chiral center, making it achiral).
Step 2: L-configuration of amino acids. Most naturally occurring amino acids are in the L-configuration, which is why they are optically active (except glycine).
Step 3: Conclusion. Thus, both Assertion (A) and Reason (R) are true, and Reason (R) correctly explains Assertion (A), making option (A) the correct answer.
(a) Define the following:
(i) Enantiomers
(ii) Racemic mixture
The CORRECT statement(s) regarding the given molecules is(are):
How many different stereoisomers are possible for the given molecule?
An object has moved through a distance can it have zero displacement if yes support your answer with an example.
Acidified \(KMnO_4\) oxidizes sulphite to:
The correct IUPAC name of \([ \text{Pt}(\text{NH}_3)_2\text{Cl}_2 ]^{2+} \) is:
Consider the following compounds:
(i) CH₃CH₂Br
(ii) CH₃CH₂CH₂Br
(iii) CH₃CH₂CH₂CH₂Br
Arrange the compounds in the increasing order of their boiling points.
Alkyl halides undergoing nucleophilic bimolecular substitution reaction involve: