The resonance structure of the hydrazoic acid molecule should be found. Concept Introduction: Sometimes the chemical bonding of a molecule cannot be represented using a single Lewis structure. In these cases, the chemical bonding are described by delocalization of electrons and is known as resonance. In some molecules, there is possibility of more than one Lewis structure where all the structures are equally acceptable. One of the acceptable Lewis structures of these molecules is called resonance structure. All the possible resonance structures are imaginary whereas the resonance hybrid is real. Any of the possible structure does not exist as such like a stable real molecule. So it is not possible to isolate one resonance structure. These structures will differ only in the arrangement of the electrons not in the relative position of the atomic nuclei. Structure with greater number of covalent bonds are more stable comparing to that with lower number of covalent bonds. Structure which does not involve charge separation is more stable when comparing with structure having positive and negative charge separation. While drawing resonance structure of a molecule some rules should be followed where the position, over whole charge and chemical framework remains intact. Also only π and nonbonding electron has been moved in all the three resonance structures

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Answer 1

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Chapter 6, Problem 6.37QP

Interpretation Introduction

Interpretation: The resonance structure of the hydrazoic acid molecule should be found.

Concept Introduction: Sometimes the chemical bonding of a molecule cannot be represented using a single Lewis structure. In these cases, the chemical bonding are described by delocalization of electrons and is known as resonance.

In some molecules, there is possibility of more than one Lewis structure where all the structures are equally acceptable. One of the acceptable Lewis structures of these molecules is called resonance structure.

All the possible resonance structures are imaginary whereas the resonance hybrid is real.

Any of the possible structure does not exist as such like a stable real molecule. So it is not possible to isolate one resonance structure.

These structures will differ only in the arrangement of the electrons not in the relative position of the atomic nuclei.

Structure with greater number of covalent bonds are more stable comparing to that with lower number of covalent bonds.

Structure which does not involve charge separation is more stable when comparing with structure having positive and negative charge separation.

While drawing resonance structure of a molecule some rules should be followed where the position, over whole charge and chemical framework remains intact. Also only π and nonbonding electron has been moved in all the three resonance structures

Interpretation Introduction

Interpretation: The formal charges of hydrazoic acid molecule should be found.

Concept Introduction

A formal charge (FC) is the charge assigned to an atom in a molecule, irrespective of relative electronegativity by thinking that electrons in all chemical bonds are shared equally among atoms.

This method is used to identify the most probable Lewis structures if more than one possibility exists for a compound.

The Lewis structure with formal charge on each of the atoms close to zero is taken as the most plausible structure.

Formal charge of an atom can be determined by the given formula.

Formal charge (F C) = (no.of valence electron in atom)−12(no.of bonding electrons)−(no.of non-bonding electrons)

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Students have asked these similar questions

The carbonate anion, CO32- , is a resonance hybrid. Draw all of the important resonance structures for this molecule. If an atom has a nonzero formal charge, be sure the formal charge is shown clearly in the structure. Use the resonance structures to calculate the average formal charge on each O atom (which are all equivalent in the "true" structure). [Note: all of the important contributing resonance structures have octets around each atom that desires an octet.]

When gaseous sulfur trioxide is dissolved in concentratedsulfuric acid, disulfuric acid forms:SO₃(g)+ H₂SO₄(l) →H₂S₂O₇(l) Use bond energies Table to determine ΔH°ᵣₓₙ. (The S atoms in H₂S₂O₇ are bonded through an O atom. Assume Lewis structures with zero formal charges; BE of SNO is 552 kJ/mol.)

Write all resonance structures for NCO− ion. Use formal charges to predict the most stable one (i.e. the one that has the lowest energy configuration) and the least stable. Briefly explain.

Answer 2

Question

Chapter 6, Problem 6.37QP

Interpretation Introduction

Interpretation: The resonance structure of the hydrazoic acid molecule should be found.

Concept Introduction: Sometimes the chemical bonding of a molecule cannot be represented using a single Lewis structure. In these cases, the chemical bonding are described by delocalization of electrons and is known as resonance.

In some molecules, there is possibility of more than one Lewis structure where all the structures are equally acceptable. One of the acceptable Lewis structures of these molecules is called resonance structure.

All the possible resonance structures are imaginary whereas the resonance hybrid is real.

Any of the possible structure does not exist as such like a stable real molecule. So it is not possible to isolate one resonance structure.

These structures will differ only in the arrangement of the electrons not in the relative position of the atomic nuclei.

Structure with greater number of covalent bonds are more stable comparing to that with lower number of covalent bonds.

Structure which does not involve charge separation is more stable when comparing with structure having positive and negative charge separation.

While drawing resonance structure of a molecule some rules should be followed where the position, over whole charge and chemical framework remains intact. Also only π and nonbonding electron has been moved in all the three resonance structures

Interpretation Introduction

Interpretation: The formal charges of hydrazoic acid molecule should be found.

Concept Introduction

A formal charge (FC) is the charge assigned to an atom in a molecule, irrespective of relative electronegativity by thinking that electrons in all chemical bonds are shared equally among atoms.

This method is used to identify the most probable Lewis structures if more than one possibility exists for a compound.

The Lewis structure with formal charge on each of the atoms close to zero is taken as the most plausible structure.

Formal charge of an atom can be determined by the given formula.

Formal charge (F C) = (no.of valence electron in atom)−12(no.of bonding electrons)−(no.of non-bonding electrons)

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Answer 3

Question

Chapter 6, Problem 6.37QP

Interpretation Introduction

Interpretation: The resonance structure of the hydrazoic acid molecule should be found.

Concept Introduction: Sometimes the chemical bonding of a molecule cannot be represented using a single Lewis structure. In these cases, the chemical bonding are described by delocalization of electrons and is known as resonance.

In some molecules, there is possibility of more than one Lewis structure where all the structures are equally acceptable. One of the acceptable Lewis structures of these molecules is called resonance structure.

All the possible resonance structures are imaginary whereas the resonance hybrid is real.

Any of the possible structure does not exist as such like a stable real molecule. So it is not possible to isolate one resonance structure.

These structures will differ only in the arrangement of the electrons not in the relative position of the atomic nuclei.

Structure with greater number of covalent bonds are more stable comparing to that with lower number of covalent bonds.

Structure which does not involve charge separation is more stable when comparing with structure having positive and negative charge separation.

While drawing resonance structure of a molecule some rules should be followed where the position, over whole charge and chemical framework remains intact. Also only π and nonbonding electron has been moved in all the three resonance structures

Interpretation Introduction

Interpretation: The formal charges of hydrazoic acid molecule should be found.

Concept Introduction

A formal charge (FC) is the charge assigned to an atom in a molecule, irrespective of relative electronegativity by thinking that electrons in all chemical bonds are shared equally among atoms.

This method is used to identify the most probable Lewis structures if more than one possibility exists for a compound.

The Lewis structure with formal charge on each of the atoms close to zero is taken as the most plausible structure.

Formal charge of an atom can be determined by the given formula.

Formal charge (F C) = (no.of valence electron in atom)−12(no.of bonding electrons)−(no.of non-bonding electrons)

Expert Solution & Answer

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Answer 4

Question

Chapter 6, Problem 6.37QP

Interpretation Introduction

Interpretation: The resonance structure of the hydrazoic acid molecule should be found.

Concept Introduction: Sometimes the chemical bonding of a molecule cannot be represented using a single Lewis structure. In these cases, the chemical bonding are described by delocalization of electrons and is known as resonance.

In some molecules, there is possibility of more than one Lewis structure where all the structures are equally acceptable. One of the acceptable Lewis structures of these molecules is called resonance structure.

All the possible resonance structures are imaginary whereas the resonance hybrid is real.

Any of the possible structure does not exist as such like a stable real molecule. So it is not possible to isolate one resonance structure.

These structures will differ only in the arrangement of the electrons not in the relative position of the atomic nuclei.

Structure with greater number of covalent bonds are more stable comparing to that with lower number of covalent bonds.

Structure which does not involve charge separation is more stable when comparing with structure having positive and negative charge separation.

While drawing resonance structure of a molecule some rules should be followed where the position, over whole charge and chemical framework remains intact. Also only π and nonbonding electron has been moved in all the three resonance structures

Interpretation Introduction

Interpretation: The formal charges of hydrazoic acid molecule should be found.

Concept Introduction

A formal charge (FC) is the charge assigned to an atom in a molecule, irrespective of relative electronegativity by thinking that electrons in all chemical bonds are shared equally among atoms.

This method is used to identify the most probable Lewis structures if more than one possibility exists for a compound.

The Lewis structure with formal charge on each of the atoms close to zero is taken as the most plausible structure.

Formal charge of an atom can be determined by the given formula.

Formal charge (F C) = (no.of valence electron in atom)−12(no.of bonding electrons)−(no.of non-bonding electrons)

Expert Solution & Answer

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Check out a sample textbook solution

See solution

Answer 5

Chapter 6, Problem 6.37QP

Interpretation Introduction

Interpretation: The resonance structure of the hydrazoic acid molecule should be found.

Concept Introduction: Sometimes the chemical bonding of a molecule cannot be represented using a single Lewis structure. In these cases, the chemical bonding are described by delocalization of electrons and is known as resonance.

In some molecules, there is possibility of more than one Lewis structure where all the structures are equally acceptable. One of the acceptable Lewis structures of these molecules is called resonance structure.

All the possible resonance structures are imaginary whereas the resonance hybrid is real.

Any of the possible structure does not exist as such like a stable real molecule. So it is not possible to isolate one resonance structure.

These structures will differ only in the arrangement of the electrons not in the relative position of the atomic nuclei.

Structure with greater number of covalent bonds are more stable comparing to that with lower number of covalent bonds.

Structure which does not involve charge separation is more stable when comparing with structure having positive and negative charge separation.

While drawing resonance structure of a molecule some rules should be followed where the position, over whole charge and chemical framework remains intact. Also only π and nonbonding electron has been moved in all the three resonance structures

Interpretation Introduction

Interpretation: The formal charges of hydrazoic acid molecule should be found.

Concept Introduction

A formal charge (FC) is the charge assigned to an atom in a molecule, irrespective of relative electronegativity by thinking that electrons in all chemical bonds are shared equally among atoms.

This method is used to identify the most probable Lewis structures if more than one possibility exists for a compound.

The Lewis structure with formal charge on each of the atoms close to zero is taken as the most plausible structure.

Formal charge of an atom can be determined by the given formula.

Formal charge (F C) = (no.of valence electron in atom)−12(no.of bonding electrons)−(no.of non-bonding electrons)

Answer 6

Chapter 6, Problem 6.37QP

Interpretation Introduction

Interpretation: The resonance structure of the hydrazoic acid molecule should be found.

Concept Introduction: Sometimes the chemical bonding of a molecule cannot be represented using a single Lewis structure. In these cases, the chemical bonding are described by delocalization of electrons and is known as resonance.

In some molecules, there is possibility of more than one Lewis structure where all the structures are equally acceptable. One of the acceptable Lewis structures of these molecules is called resonance structure.

All the possible resonance structures are imaginary whereas the resonance hybrid is real.

Any of the possible structure does not exist as such like a stable real molecule. So it is not possible to isolate one resonance structure.

These structures will differ only in the arrangement of the electrons not in the relative position of the atomic nuclei.

Structure with greater number of covalent bonds are more stable comparing to that with lower number of covalent bonds.

Structure which does not involve charge separation is more stable when comparing with structure having positive and negative charge separation.

While drawing resonance structure of a molecule some rules should be followed where the position, over whole charge and chemical framework remains intact. Also only π and nonbonding electron has been moved in all the three resonance structures

Answer 7

Chapter 6, Problem 6.37QP

Interpretation Introduction

Interpretation: The resonance structure of the hydrazoic acid molecule should be found.

Concept Introduction: Sometimes the chemical bonding of a molecule cannot be represented using a single Lewis structure. In these cases, the chemical bonding are described by delocalization of electrons and is known as resonance.

In some molecules, there is possibility of more than one Lewis structure where all the structures are equally acceptable. One of the acceptable Lewis structures of these molecules is called resonance structure.

All the possible resonance structures are imaginary whereas the resonance hybrid is real.

Any of the possible structure does not exist as such like a stable real molecule. So it is not possible to isolate one resonance structure.

These structures will differ only in the arrangement of the electrons not in the relative position of the atomic nuclei.

Structure with greater number of covalent bonds are more stable comparing to that with lower number of covalent bonds.

Structure which does not involve charge separation is more stable when comparing with structure having positive and negative charge separation.

While drawing resonance structure of a molecule some rules should be followed where the position, over whole charge and chemical framework remains intact. Also only π and nonbonding electron has been moved in all the three resonance structures

Answer 8

Interpretation Introduction

Interpretation: The formal charges of hydrazoic acid molecule should be found.

Concept Introduction

A formal charge (FC) is the charge assigned to an atom in a molecule, irrespective of relative electronegativity by thinking that electrons in all chemical bonds are shared equally among atoms.

This method is used to identify the most probable Lewis structures if more than one possibility exists for a compound.

The Lewis structure with formal charge on each of the atoms close to zero is taken as the most plausible structure.

Formal charge of an atom can be determined by the given formula.

Formal charge (F C) = (no.of valence electron in atom)−12(no.of bonding electrons)−(no.of non-bonding electrons)

Answer 9

Interpretation Introduction

Interpretation: The formal charges of hydrazoic acid molecule should be found.

Concept Introduction

A formal charge (FC) is the charge assigned to an atom in a molecule, irrespective of relative electronegativity by thinking that electrons in all chemical bonds are shared equally among atoms.

This method is used to identify the most probable Lewis structures if more than one possibility exists for a compound.

The Lewis structure with formal charge on each of the atoms close to zero is taken as the most plausible structure.

Formal charge of an atom can be determined by the given formula.

Formal charge (F C) = (no.of valence electron in atom)−12(no.of bonding electrons)−(no.of non-bonding electrons)

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 6.2 - Classify the following bonds as nonpolar, polar,...Ch. 6.2 - Classify the following bonds as nonpolar, polar,...Ch. 6.2 - Prob. 1PPB Ch. 6.2 - Electrostatic potential maps are shown for HCl and...Ch. 6.2 - Prob. 6.2WE Ch. 6.2 - Prob. 2PPA Ch. 6.2 - Prob. 2PPB Ch. 6.2 - Prob. 2PPC Ch. 6.2 - Prob. 6.3WE Ch. 6.2 - Prob. 3PPA

Solution Summary: The author explains that the chemical bonding of a molecule can't be represented using'single' Lewis structures, which are described by delocalization of electrons.

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