ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
6th Edition
ISBN: 9781319306977
Author: LOUDON
Publisher: INTER MAC
Question
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Chapter 6, Problem 6.43AP
Interpretation Introduction

(a)

Interpretation:

The age of the skull sample is to be calculated.

Concept introduction:

A carbon atom that has four nonequivalent atoms or groups attached to it is known as the chiral carbon atom. Chiral carbon centers are also called asymmetric or stereogenic centers. A chiral molecule is an optically active molecule. It rotates the plane of a plane polarized light. The specific optical rotation of a compound is given by the expression as shown below.

[α]=αcl

Expert Solution
Check Mark

Answer to Problem 6.43AP

The age of the skull sample is 205.128yr.

Explanation of Solution

The rate of racemization in skull samples follows the equation

ln(1+r1r)=kt …(1)

Where,

  • k is the rate constant (6.24×104yr1).
  • t is the age of the sample in years.
  • r is the ratio of (R)-()- and (S)-(+)- aspartic acid.

The percentage of (R)-()- aspartic acid in the skull sample is 6%.

The percentage of (S)-(+)- aspartic acid in the skull sample is 94%.

The expression for r is shown below,

r=P%(R)P%(S) …(2)

Where,

  • P%(R) is the percentage of (R)-()- aspartic acid.
  • P%(S) is the percentage of (S)-(+)- aspartic acid.

Substitute the value of P%(R) and P%(S) in the equation (2).

r=6%94%=0.064

Substitute the values of r and k in the equation (1).

ln(1+0.06410.064)=(6.24×104yr1)tln(1.0640.936)=(6.24×104yr1)tln(1.0640.936)=(6.24×104yr1)t0.128=(6.24×104yr1)t

Rearrange the above expression for the value of t.

t=0.1286.24×104yr1=205.128yr

Therefore, the age of the skull sample is 205.128yr.

Conclusion

The age of the skull sample is 205.128yr.

Interpretation Introduction

(b)

Interpretation:

The enantiomeric excess of the (S)-(+)- aspartic acid in the sample is to be calculated.

Concept introduction:

A carbon atom that has four nonequivalent atoms or groups attached to it is known as the chiral carbon atom. Chiral carbon centers are also called asymmetric or stereogenic centers. A chiral molecule is an optically active molecule. It rotates the plane of a plane polarized light. The specific optical rotation of a compound is given by the expression as shown below.

[α]=αcl

Expert Solution
Check Mark

Answer to Problem 6.43AP

The enantiomeric excess of the (S)-(+)- aspartic acid in the sample is 88%.

Explanation of Solution

The percentage of (R)-()- aspartic acid in the skull sample is 6%.

The percentage of (S)-(+)- aspartic acid in the skull sample is 94%.

The enantiomeric excess of a sample is given by the formula as shown below.

EE=2(%majorenantiomer)100%

Substitute the value of percentage of (S)-(+)- aspartic acid in the skull sample in the above equation.

EE=2(94%)100%=88%

Therefore, The enantiomeric excess of the (S)-(+)- aspartic acid in the sample is 88%.

Conclusion

The enantiomeric excess of the (S)-(+)- aspartic acid in the sample is 88%.

Interpretation Introduction

(c)

Interpretation:

The observed rotation of 100mg of the forensic sample in 10mL of 6M aqueous HCl is to be calculated.

Concept introduction:

A carbon atom that has four nonequivalent atoms or groups attached to it is known as the chiral carbon atom. Chiral carbon centers are also called asymmetric or stereogenic centers. A chiral molecule is an optically active molecule. It rotates the plane of a plane polarized light. The specific optical rotation of a compound is given by the expression as shown below.

[α]=αcl

Expert Solution
Check Mark

Answer to Problem 6.43AP

The observed rotation of 100mg of the forensic sample in 10mL of 6M aqueous HCl is 0.2156degrees.

Explanation of Solution

The specific rotation of (S)-(+)-aspartic acid, [α]D20=+24.5degreesmLg1dm1.

The mass of the forensic sample is 100mg.

The volume of 6M aqueous HCl is 10mL.

The standard path length is 1dm.

The enantiomeric excess of the (S)-(+)- aspartic acid in the sample is 88%.

The specific rotation of the mixture is given by the expression as shown below.

EE=100%×[α]mixture[α]pure

Where,

  • [α]mixture is the specific rotation of the mixture.
  • [α]pure is the specific rotation of the pure enantiomer.

Rearrange the above equation for the value of [α]mixture.

Substitute the value of [α]mixture and [α]pure in the above equation.

[α]mixture=EE×[α]pure100%

Substitute the value of EE and [α]pure in the above equation.

[α]mixture=(88%)(+24.5degreesmLg1dm1)100%=+21.56degreesmLg1dm1

The concentration of solution is given by the formula as shown below.

c=mV

Where,

  • m is the mass of the solute.
  • V is the volume of the solution.

Substitute the value of and in the above equation.

c=(100mg10mL)(1g1000mg)=0.01gmL1

The observed rotation of a compound is given by the expression as shown below.

α=cl[α] …(3)

Where,

  • α is the observed rotation.
  • [α] is the specific rotation.
  • c is the concentration of the solution in gmL1.
  • l is the path length in dm.

Substitute the value of [α], c and l in the equation (3).

α=(0.01gmL1)(1dm)(+21.56degreesmLg1dm1)=0.2156degrees

Therefore, the observed rotation of 100mg of the forensic sample in 10mL of 6M aqueous HCl is 0.2156degrees.

Conclusion

The observed rotation of 100mg of the forensic sample in 10mL of 6M aqueous HCl is 0.2156degrees.

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