A) It has no optical rotation. B) It cannot be superimposed on its mirror image. C) It has a linear structure. D) It has no stereocenters.
A) An atom that is bonded to two groups. B) An atom that is bonded to four different groups. C) An atom that is bonded to three different groups. D) An atom that is bonded to four identical groups.
A) 4 B) 2 C) 3 D) 1
A) Visible light. B) Infrared light. C) Plane-polarized light. D) Ultraviolet light.
A) By counting the number of carbons in a molecule. B) By measuring optical activity with a polarimeter. C) By checking the molecular weight of a compound. D) By analyzing the color of the substance.
A) A mixture of meso compounds. B) A mixture of diastereomers. C) A mixture of structurally different molecules. D) A 50:50 mixture of two enantiomers.
A) They can have different biological effects. B) They have no medicinal value. C) They have the same properties in the body. D) They are easier to synthesize.
A) A compound with no stereocenters. B) A compound with high molecular weight. C) A compound that rotates the plane of polarized light. D) A compound that absorbs light.
A) Enantiomers have identical physical properties except for optical activity. B) Chiral molecules are always more soluble than achiral molecules. C) Racemic mixtures have higher melting points than pure enantiomers. D) Diastereomers have identical boiling points. |