Which of the following cyclic molecules are meso compounds?

a.

b.

c.

Short Answer

Expert verified
  1. Not a meso
  2. Meso
  3. Not a meso

Step by step solution

01

Meso compound 

A compound is said to be meso if it follows two conditions given below:

  • Two or more chiral centers.
  • Plane of symmetry.
02

Plane of symmetry

The plane of symmetry is present when a molecule has the same groups at both sides of the plane.

03

Explanation

a. The molecule has two chiral centers due to the presence of four different groups at each chiral center.

One chiral center has a methyl group above the plane and one methyl group below the plane. Therefore, the molecule does not have any plane of symmetry (neither horizontal nor vertical).

Hence, the molecule is not a meso compound.

Not a meso compound

b. The molecule has two chiral centers, and both the methyl groups are present above the plane. Therefore, a plane passes through the middle of the carbon and divides the molecule into two equal halves.

Hence, the molecule is a meso compound.

Meso compound

c. The molecule has two chiral centers, but the groups at each chiral center are different. Therefore, the molecule does not have any plane. Hence, the molecule is not a meso compound.

Not a meso compound

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Most popular questions from this chapter

Amygdalin, a compound isolated from the pits of apricots, peaches, and wild cherries, has been used as an unsanctioned anticancer drug both within and outside of the United States. One hydrolysis product formed from amygdalin is mandelic acid, used in treating common skin problems caused by photo-aging and acne.

a. How many stereogenic centres are present in amygdalin? What is the maximum number of stereoisomers possible?

b. Draw both enantiomers of mandelic acid and label each stereogenic centre as R or S.

c. Pure (R)-mandelic acid has a specific rotation of –154. If a sample contains 60% of the R isomer and 40% of its enantiomer, what is [α]of this solution?

d. Calculate the ee of a solution of mandelic acid having [α] = +50. What is the percentage of each enantiomer present?

Draw the structure of (S)-citalopram, a drug used to treat depression and anxiety that is much more potent than its R enantiomer.

citalopram

Label each compound as chiral or achiral. Compounds that contain a single carbon common to two rings are called spiro compounds. Because carbon is tetrahedral, the two rings are perpendicular to each other.

a.

b.

c.

d.

The facts in Section 5.4A can be used to locate stereogenic centers in any molecule, no matter how complicated. Always look for carbons surrounded by four different groups. With this in mind, locate the four stereogenic centers in aliskiren, a drug introduced in 2007 for the treatment of hypertension.

The [α] of pure quinine, an antimalarial drug, is –165.

a. Calculate the ee of a solution with the following [α] values: –50, –83, and –120.

b. For each ee, calculate the percent of each enantiomer present.

c. What is [α] for the enantiomer of quinine?

d. If a solution contains 80% quinine and 20% of its enantiomer, what is the ee of the solution?

e. What is [α] for the solution described in part (d)?

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