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 1.9P
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
Problem Draw a Lewis structure and identify the octet-rule exception for (a) H3PO4 (draw two resonance forms and select the more important); (b) BFCl2.Plan We draw each Lewis structure and examine it for exceptions to the octet rule.(a) The central atom is in Period 3, so it can have more than an octet.(b) The central atom is B, which can have fewer than an octet of electrons.
Problem Which of the following substances exhibits H bonding? For any that do, show the H bonds between two of its molecules. (a) C̟H, (b) CH;OH (c) CH3C–NH,
Problem Name each of the following anions and give the name and formula of the acid derived from it: (a) Br-; (b) IO3 -; (c) CN-; (d) SO4 2-; (e) NO2 -.

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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