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
Question
Book Icon
Chapter 1, Problem 1.62P
Interpretation Introduction

(a)

Interpretation:

Given Lewis structure is to be drawn using line structure.

Concept introduction:

Line structures are compact like condensed structures. When drawing line structures, carbon atoms and hydrogen atoms attached to them are not drawn explicitly. A carbon atom is implied at the intersection of two bonds and at the end of each bond. All the other atoms except carbon and hydrogen are shown explicitly. Non-bonding electrons are usually not shown unless they are important to emphasize an aspect of the atom.

Interpretation Introduction

(b)

Interpretation:

Given Lewis structure is to be drawn using line structure.

Concept introduction:

Line structures are compact like condensed structures. When drawing line structures, carbon atoms and the hydrogen atoms attached to them are not drawn explicitly. A carbon atom is implied at the intersection of two bonds and at the end of each bond. All the other atoms except carbon and hydrogen are shown explicitly. Non-bonding electrons are usually not shown unless they are important to emphasize an aspect of the atom.

Interpretation Introduction

(c)

Interpretation:

Given Lewis structure is to be drawn using line structure.

Concept introduction:

Line structures are compact like condensed structures. When drawing line structures, carbon atoms and the hydrogen atoms attached to them are not drawn explicitly. A carbon atom is implied at the intersection of two bonds and at the end of each bond. All the other atoms except carbon and hydrogen are shown explicitly. Non-bonding electrons are usually not shown unless they are important to emphasize an aspect of the atom.

Interpretation Introduction

(d)

Interpretation:

Given Lewis structure is to be drawn using line structure.

Concept introduction:

Line structures are compact like condensed structures. When drawing line structures, carbon atoms and the hydrogen atoms attached to them are not drawn explicitly. A carbon atom is implied at the intersection of two bonds and at the end of each bond. All the other atoms except carbon and hydrogen are shown explicitly. Non-bonding electrons are usually not shown unless they are important to emphasize an aspect of the atom.

Interpretation Introduction

(e)

Interpretation:

Given Lewis structure is to be drawn using line structure.

Concept introduction:

Line structures are compact like condensed structures. When drawing line structures, carbon atoms and the hydrogen atoms attached to them are not drawn explicitly. A carbon atom is implied at the intersection of two bonds and at the end of each bond. All the other atoms except carbon and hydrogen are shown explicitly. Non-bonding electrons are usually not shown unless they are important to emphasize an aspect of the atom.

Interpretation Introduction

(f)

Interpretation:

Given Lewis structure is to be drawn using line structure.

Concept introduction:

Line structures are compact like condensed structures. When drawing line structures, carbon atoms and the hydrogen atoms attached to them are not drawn explicitly. A carbon atom is implied at the intersection of two bonds and at the end of each bond. All the other atoms except carbon and hydrogen are shown explicitly. Non-bonding electrons are usually not shown unless they are important to emphasize an aspect of the atom.

Blurred answer
Students have asked these similar questions
A 1.88/The curved arrow notation introduced in Section 1.6B is a powerful method used by organic chemists to show the movement of electrons not only in resonance structures, but also in chemical reactions. Because each curved arrow shows the movement of two electrons, following the curved arrows illustrates what bonds are broken and formed in a reaction. Consider the following three-step process. (a) Add curved arrows in Step [1] to show the movement of electrons. (b) Use the curved arrows drawn in Step [2] to identify the structure of X. X is converted in Step [3] to phenol and HCI. H [1] + H-i: + :ÖH HO [2] + H-i: [3] phenol
(a) Draw a line drawing for the Lewis diagram given below. Hint start converting the Lewis to a VSEPR diagram. H H H +4 H H (b) What is the line drawing for a chemical species with the condensed molecular formula -H CH3CHC(CH3)CH(CH3)2. Hint start by converting the condensed formula to a Lewis diagram....then you solve this just like Question 1(a)!. (c) Of course, concepts can be examined in reverse! Draw a VSEPR diagram THAT IS ALSO A BEST LEWIS DIAGRAM, for the chemical that has the following line drawing: H₂N IO
Which compound contains the most polar bond? (A) (B) F (C) (D) Compound D Compound C O Compound A Compound B uestion oC

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
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Text book image
Chemistry: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning