Question 1
Which configuration results when the sequence of priority groups around a chiral center is clockwise?
Question 2
Which compound is optically inactive despite having chiral centers?
Question 3
What does the term 'achiral' refer to?
Question 4
What is a characteristic feature of racemic mixtures?
Question 5
What is the main difference between constitutional isomers and configurational isomers?
Question 6
How would you determine the configuration if the priority 4 group is in front of the plane (on a wedge)?
Question 7
In Fisher projections, how are horizontal lines typically interpreted?
Question 8
Which stereoisomers differ in configuration at only some (but not all) chiral centers?
Question 9
What is a chiral center?
Question 10
What kind of isomerism do E and Z forms represent?
Question 11
Which configuration label would be assigned if the direction of priority groups around a chiral center is counterclockwise?
Question 12
When assigning priorities based on atomic number, which priority number is given to the group with the highest atomic number?
Question 13
Which type of optical rotation corresponds to a dextrorotary substance?
Question 14
What distinguishes diastereomers from enantiomers?
Question 15
How are enantiomers related in terms of their configuration at chiral centers?