Organic Chemistry: Principles and Mechanisms (Second Edition)
Organic Chemistry: Principles and Mechanisms (Second Edition)
2nd Edition
ISBN: 9780393663556
Author: Joel Karty
Publisher: W. W. Norton & Company
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Chapter 1, Problem 1.45P
Interpretation Introduction

(a)

Interpretation:

Whether the given structure is a legitimate Lewis structure is to be determined.

Concept introduction:

For a valid Lewis structure of a molecule, the atoms must not exceed their normal valency. In general, this means atoms from the 2nd row onward of the periodic table must follow the octet rule. The exceptions to this rule are elements from the third row like S, P, etc., which are capable of expanding their octets to a maximum of twelve valence electrons. A hydrogen atom cannot have more than two valence electrons.

Interpretation Introduction

(b)

Interpretation:

Whether the given structure is a legitimate Lewis structure is to be determined.

Concept introduction:

For a valid Lewis structure of a molecule, the atoms must not exceed their normal valency. In general, this means atoms from the 2nd row onward of the periodic table must follow the octet rule. The exceptions to this rule are elements from the third row like S, P, etc., which are capable of expanding their octets to a maximum of twelve valence electrons. A hydrogen atom cannot have more than two valence electrons.

Interpretation Introduction

(c)

Interpretation:

Whether the given structure is a legitimate Lewis structure is to be determined.

Concept introduction:

For a valid Lewis structure of a molecule, the atoms must not exceed their normal valency. In general, this means atoms from the 2nd row onward of the periodic table must follow the octet rule. The exceptions to this rule are elements from the third row like S, P, etc., which are capable of expanding their octets to a maximum of twelve valence electrons. A hydrogen atom cannot have more than two valence electrons.

Interpretation Introduction

(d)

Interpretation:

Whether the given structure is a legitimate Lewis structure is to be determined.

Concept introduction:

For a valid Lewis structure of a molecule, the atoms must not exceed their normal valency. In general, this means atoms from the 2nd row onward of the periodic table must follow the octet rule. The exceptions to this rule are elements from the third row like S, P, etc., which are capable of expanding their octets to a maximum of twelve valence electrons. A hydrogen atom cannot have more than two valence electrons.

Interpretation Introduction

(e)

Interpretation:

Whether the given structure is a legitimate Lewis structure is to be determined.

Concept introduction:

For a valid Lewis structure of a molecule the atoms must not exceed their normal valency. In general, this means atoms from the 2nd row onward of the periodic table must follow the octet rule. The exceptions to this rule are elements from the third row like S, P, etc., which are capable of expanding their octets to a maximum of twelve valence electrons. A hydrogen atom cannot have more than two valence electrons.

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Students have asked these similar questions
1. Add nonbonding electron pairs to each atom where it is implied by the line-angle drawings shown below. 2. Use the curved arrow formalism to generate four additional, valid resonance structures for each compound. 3. Rank your resonance structures in order of increasing contribution to the overall nature of the molecule.
Please help me with this, I have attached two images which are incorrect answers, I now want to study, lone pairs DO NOT MATTER, only charge and structure.
Do not give handwriting solution.   What is the formal charge of structure C?

Chapter 1 Solutions

Organic Chemistry: Principles and Mechanisms (Second Edition)

Ch. 1 - Prob. 1.11PCh. 1 - Prob. 1.12PCh. 1 - Prob. 1.13PCh. 1 - Prob. 1.14PCh. 1 - Prob. 1.15PCh. 1 - Prob. 1.16PCh. 1 - Prob. 1.17PCh. 1 - Prob. 1.18PCh. 1 - Prob. 1.19PCh. 1 - Prob. 1.20PCh. 1 - Prob. 1.21PCh. 1 - Prob. 1.22PCh. 1 - Prob. 1.23PCh. 1 - Prob. 1.24PCh. 1 - Prob. 1.25PCh. 1 - Prob. 1.26PCh. 1 - Prob. 1.27PCh. 1 - Prob. 1.28PCh. 1 - Prob. 1.29PCh. 1 - Prob. 1.30PCh. 1 - Prob. 1.31PCh. 1 - Prob. 1.32PCh. 1 - Prob. 1.33PCh. 1 - Prob. 1.34PCh. 1 - Prob. 1.35PCh. 1 - Prob. 1.36PCh. 1 - Prob. 1.37PCh. 1 - Prob. 1.38PCh. 1 - Prob. 1.39PCh. 1 - Prob. 1.40PCh. 1 - Prob. 1.41PCh. 1 - Prob. 1.42PCh. 1 - Prob. 1.43PCh. 1 - Prob. 1.44PCh. 1 - Prob. 1.45PCh. 1 - Prob. 1.46PCh. 1 - Prob. 1.47PCh. 1 - Prob. 1.48PCh. 1 - Prob. 1.49PCh. 1 - Prob. 1.50PCh. 1 - Prob. 1.51PCh. 1 - Prob. 1.52PCh. 1 - Prob. 1.53PCh. 1 - Prob. 1.54PCh. 1 - Prob. 1.55PCh. 1 - Prob. 1.56PCh. 1 - Prob. 1.57PCh. 1 - Prob. 1.58PCh. 1 - Prob. 1.59PCh. 1 - Prob. 1.60PCh. 1 - Prob. 1.61PCh. 1 - Prob. 1.62PCh. 1 - Prob. 1.63PCh. 1 - Prob. 1.64PCh. 1 - Prob. 1.65PCh. 1 - Prob. 1.66PCh. 1 - Prob. 1.67PCh. 1 - Prob. 1.68PCh. 1 - Prob. 1.69PCh. 1 - Prob. 1.70PCh. 1 - Prob. 1.71PCh. 1 - Prob. 1.72PCh. 1 - Prob. 1.73PCh. 1 - Prob. 1.74PCh. 1 - Prob. 1.75PCh. 1 - Prob. 1.76PCh. 1 - Prob. 1.77PCh. 1 - Prob. 1.78PCh. 1 - Prob. 1.79PCh. 1 - Prob. 1.80PCh. 1 - Prob. 1.81PCh. 1 - Prob. 1.82PCh. 1 - Prob. 1.1YTCh. 1 - Prob. 1.2YTCh. 1 - Prob. 1.3YTCh. 1 - Prob. 1.4YTCh. 1 - Prob. 1.5YTCh. 1 - Prob. 1.6YTCh. 1 - Prob. 1.7YTCh. 1 - Prob. 1.8YTCh. 1 - Prob. 1.9YTCh. 1 - Prob. 1.10YTCh. 1 - Prob. 1.11YTCh. 1 - Prob. 1.12YTCh. 1 - Prob. 1.13YTCh. 1 - Prob. 1.14YTCh. 1 - Prob. 1.15YTCh. 1 - Prob. 1.16YTCh. 1 - Prob. 1.17YT
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