BIOLOGY
AMINO ACIDS
Question
[CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
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2-aminoethanoic acid
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2-aminopropanoic acid
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3-amino-3-methylbuthanoic acid
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2-amino-2-methylpropanoic acid
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Detailed explanation-1: -The 2-aminopropanoic acid will exist in optically active form as it contains an asymmetric C atom which is a C atom to which 4 different atoms or groups are attached.
Detailed explanation-2: -2-aminopropanoic acid (alanine) has two enantiomers (optical isomers) because it has a chiral molecule containing an asymmetric carbon atom. One enantiomer is a non-superimposable mirror image of the other.
Detailed explanation-3: -2-hydroxypropanoic acid has a central carbon atom, which is linked to four different groups. This carbon atom is called chiral carbon atom and the molecule is called chiral molecule. Hence, 2-hydroxypropanoic acid shows optical isomerism.
Detailed explanation-4: -A chiral molecule that rotates light is said to be optically active. If the molecule rotates the plane-polarized light in the clockwise direction, we call that rotation a dextrorotatory rotation. However, if the light rotates counterclockwise, we call that rotation levorotatory.