Chapter 15.4, Problem 5PTS

 (a)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.

To Identify: The number of proton signals the structure would exhibits.

 (b)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.

 (c)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.

 (d)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.

 (e)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.

 (f)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.

 (g)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.

 (h)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.

 (i)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.

 (j)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.

 (k)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.

(l)

Interpretation Introduction

Interpretation: For a given set of molecules the number of signals expected in ${}^{\text{1}}\text{H}\text{NMR}$ spectrum to be identified.

Concept Introduction:

${}^{\text{1}}\text{H NMR}$: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

Homotopic: If the protons are interchangeable through rotational symmetry, then the protons are chemically equivalent and termed as homotopic.

Enantiotopic protons: If subjected protons in the molecule can be interchanged through rotational or reflection symmetry known as Enantiotopic protons and the protons are chemically equivalent.

Diastereotopic: If the protons are not interchangeable through either of the symmetry operations, then the protons are Diastereotopic; the protons are not chemically equivalent if a chiral center present in the molecule.

Replacement test: In the molecule replacing each one of the subjected protons with deuterium gives the two compounds are same; then the protons are chemically equivalent.