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)?

Short Answer

Expert verified

a. The value of ee for[α] values, –50, –83, and –120 are 30%, 50%, and 73%, respectively.

b. The values are mentioned below:

  • For 30% ee, the amount of quinine and quinine’s enantiomer are 65% and 35%, respectively.
  • For 50% ee, the amount of quinine and quinine’s enantiomer are 75% and 25%, respectively.
  • For 73% ee, the amount of quinine and quinine’s enantiomer are 86.5% and 13.5%, respectively.

c. The value of [α] for enantiomer of quinine is +165.

d. The ee of the solution is 60%.

e. The value of [α] of the solution in part (d) is -99.

Step by step solution

01

Formula for ee calculation

The formula that is used to calculate ee is given as follows:

ee=αmixtureαpureenantiomer×100%

02

Explanation for a, b, and c

a. The[α] values are given as –50, –83, and –120. The calculation of ee for each value is shown below:

Substitute the values in the formula.

ee=-50-165×100%=30%

ee=-83-165×100%=50.3%

ee=-120-165×100%=72.7%

Thus, the value of ee for [α] values, –50, –83, and –120, are 30%, 50%, and 73%, respectively.

b. The % ee value represents the excess of one compound, and the remaining of it contains the mixture of 2 compounds equally.

For 30% ee, 30% represents the excess of quinine, and 70% remaining contains a mixture of 2 compounds; quinine and quinine’s enantiomer.

The amount of quinine and quinine’s enantiomer is calculated as follows:

localid="1648533965427" Amountofquinine=30+35=65%Amountofquinineenantiomer=35%

For 50% ee, 50% represents the excess of quinine, and 50% remaining contains a mixture of 2 compounds; quinine and quinine’s enantiomer.

The amount of quinine and quinine’s enantiomer is calculated as follows:

localid="1648533974379" Amountofquinine=50+35=75%Amountofquinineenantiomer=25%

For 73% ee, 50% represents the excess of quinine, and 27% remaining contains a mixture of 2 compounds; quinine and quinine’s enantiomer.

The amount of quinine and quinine’s enantiomer is calculated as follows:

localid="1648533984709" Amountofquinine=73+35=86.5%Amountofquinineenantiomer=13.5%

c. The value of [α] for a pure enantiomer is given as -165. Thus, the enantiomer of quinine is +165.

03

Explanation for d and e

d. The ee values are given as 80% quinine and 20% of its enantiomer. The ee of the solution is calculated as follows:

Amountofsolution=80%-20%=60%

Thus, the amount of solution is 60%.

e. The ee for the solution in part (d) is calculated as follows:

60%=αmixture-165×100%αmixture=60%(-165)100%=-99

Thus, the value of [α] of the solution in part (d) is -99.

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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 all the possible stereoisomers for each compound and label pairs of enantiomers and diastereomers.

a.

b.

(S)-Lactic acid has a specific rotation of +3.8. (a) If the ee of a solution of lactic acid is 60%, what is[α]this solution? (b) How much of a dextrorotatory and levorotatory isomer does the solution contain?

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.

Explain each statement by referring to compounds A-E.

a. A has a mirror image but no enantiomer.

b. B has an enantiomer and no diastereomer.

c. C has both an enantiomer and a diastereomer.

d. D has a diastereomer but no enantiomer.

e. E has a diastereomer but no enantiomer.

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