FiltersDone

Question type

Essay

Multiple Choice

Short Answer

True False

Matching

Exam 5: Stereoisomerism

Show Answer

Share

---

All types

Filters

Study Flashcards

Question 1

Essay

Review LaterAdd Note

Review Later

Draw the meso isomer of the following compound.

Correct Answer

verified

Show Answer

Question 2

Essay

Review LaterAdd Note

Review Later

Draw the Fischer projection of the following compound.

Correct Answer

verified

Show Answer

Question 3

Short Answer

Review LaterAdd Note

Assign the absolute configuration of the chirality center as R or S.

Convert the following Fischer projection into a wedge/dash drawing.

What is the relationship between the two structures shown?

How many stereoisomers are possible for 2,3-dimethylbutane?

Draw all the isomers with molecular formula C₄H₈.

What is the relationship of the following two structures?

Which of the following is the correct IUPAC name of the following structure? SHAPE \* MERGEFORMAT

Drawn below is the structure of Singulair (montelukast), a medication used to manage athsma. Assign the absolute configuration of the chirality center as R or S.

Draw the Fischer projection of the following compound.

Draw the structure of the compound (R)-4-ethyloctane.

Drawn below is the structure of Plavix (clopidogrel), a medication used to manage blood clots. Assign the absolute configuration of the chirality center as R or S.

Draw the enantiomer of the following compound.

Which of the following structures is a correct wedge/dash drawing of the following Fischer projection?

What is the relationship between the two structures shown?

Redraw the structure below as a wedge-dash structure and label any/all stereocenters with their absolute configuration.

The structure of Crestor (rosuvastatin) , a medication used to reduce cholesterol, is shown below. If the specific rotation for this compound is known to be +100, what would be the specific rotation for the stereoisomer shown at the right?

What is the relationship of the following two structures?

What is the specific rotation of a sample of carvone that is an equal mixture of the R and S enantiomers? (R) - carvone has a specific rotation of −61.