ORGANIC CHEMISTRY-PACKAGE >CUSTOM<
ORGANIC CHEMISTRY-PACKAGE >CUSTOM<
10th Edition
ISBN: 9781260028355
Author: Carey
Publisher: MCG CUSTOM
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Chapter 16, Problem 36P

A diol ( C 8 H 18 O 2 ) does not react with periodic acid. Its H 1  NMR spectrum is shown in

Figure 16.6. What is the structure of this diol?

Chapter 16, Problem 36P, A diol (C8H18O2) does not react with periodic acid. Its H1NMR spectrum is shown in Figure 16.6. What

Expert Solution & Answer
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Interpretation Introduction

Interpretation:

The structure for the diol having molecular formula (C8H18O2) that does not react with periodic acid is to be determined from the given 1H NMR spectrum.

Concept introduction:

The vicinal diols on treatment with periodic acid (HIO4) undergo cleavage of carbon-carbon bond, where the hydroxyl groups attached and results in two carbonyl compounds.

The oxygen atoms do not show any effect on the index of hydrogen deficiency.

The index of hydrogen deficiency (IHD) represents the presence of number of multiple bonds or a ring in a molecule which can be calculated from the following formula,

IHD = 12(CnH2n+2 - CnHx)

Here, CnHx is the molecular formula of given compound.

The 1H NMR spectrum gives the information about the various hydrogen atoms in a molecule.

The chemical shift for the protons at carbon bonded to electron withdrawing group increases due to de-shielding effect.

Answer to Problem 36P

Solution: The structure for the diol having molecular formula (C8H18O2) that does not react with periodic acid is as follows:

ORGANIC CHEMISTRY-PACKAGE >CUSTOM<, Chapter 16, Problem 36P , additional homework tip  1

Explanation of Solution

As it is mentioned that the diol having molecular formula (C8H18O2) does not react with periodic acid, it must not be a vicinal diol.

As the oxygen atoms have no effect on index of hydrogen deficiency, the molecular formula of the given compound can be written as (C8H18).

Thus, the index of hydrogen deficiency in the given molecule can be calculated as follows:

Index of hydrogen deficiency = 12(CnH2n+2 - CnHx)=12(C8H2(8)+2 - C8H18)=0

This shows that the molecule does not have a ring or multiple bond. It is saturated compound.

The approximate chemical shift values from the given 1H NMR spectrum are written below:

a) 1.2δ(singlet), 12H

b) 1.6δ(singlet), 4H

c) 2.5δ(singlet), 2H

The arrangement of atoms in a molecule form the given chemical shift values are as follows:

1.2δ(singlet), 12H

The chemical shift at 1.2δ is corresponds to singlet twelve protons which describes that there are four methyl groups in a molecule. Four methyl groups cannot be bonded to single carbon, so there must be two -C(CH3)2 groups. The chemical shift value 1.2δ represents the methyl protons are de-shielded, thus the tertiary carbon bonded to methyl groups must be attached to oxygen atom. The possible connectivity is shown below:

ORGANIC CHEMISTRY-PACKAGE >CUSTOM<, Chapter 16, Problem 36P , additional homework tip  2

1.6δ(singlet), 4H

The peak at 1.6δ corresponds to singlet four protons, means there are two methylene groups bonded to tertiary carbon atom as shown below:

ORGANIC CHEMISTRY-PACKAGE >CUSTOM<, Chapter 16, Problem 36P , additional homework tip  3

2.5δ(singlet), 2H

The peak at 2.5δ corresponds to two hydroxyl groups which are bonded to the carbon having no hydrogen attached. The possible connectivity is shown below:

ORGANIC CHEMISTRY-PACKAGE >CUSTOM<, Chapter 16, Problem 36P , additional homework tip  4

Hence, the structure of diol having molecular formula (C8H18O2) is as follows:

ORGANIC CHEMISTRY-PACKAGE >CUSTOM<, Chapter 16, Problem 36P , additional homework tip  5

Conclusion

The structure of diol having molecular formula (C8H18O2) is shown.

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