Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Chapter 1.17, Problem 1.19P

1.

Interpretation Introduction

To draw: The Lewis structures for each of the given compounds.

Interpretation: The Lewis structures for each of the given compounds are to be drawn.

Concept introduction: The Lewis structure shows the connectivity between atoms by identifying the lone pairs of electrons in a compound. Lewis structures are also called Lewis dot structures. The valence electrons around an atom are shown by dots. Bonds between atoms are shown by lines and the lone pair of electrons is shown by a pair of dots.

The rules to draw Lewis structure are given as,

  • Determine the electronegativity and the number of valence electrons contributed by each atom.
  • Generally lowest electronegativity atom is the central atom.
  • Write the skeleton structure of the molecule.
  • Use two valence electrons to form each bond in skeleton structure between the central and outer atoms.
  • Satisfy the octets of atoms by distributing remaining valence electrons as nonbonding electrons. It is usually best start with the outer atoms.

2.

Interpretation Introduction

To determine: The hybridization, geometry and approximate bond angles around each of the given atom other than hydrogen.

Interpretation: The hybridization and approximate bond angles around each of the given atom other than hydrogen are to be shown.

Concept introduction: The hybridization is a theoretical phenomenon which explains the bonding pattern within the molecule. There are various types of hybridization involved in chemical bonding. Generally three main types are as follows,

  • sp
  • sp2
  • sp3

The bond angles in “sp”, “sp2” and “sp3” hybridization are 180°,120° and 109.5° respectively.

Geometry of molecules is decided by three-dimensional representation of the molecules. It involves general shape of the molecules. It also includes bond lengths, bond angles, and other parameters related to the arrangement of electrons like bond pairs and lone pairs. Geometry of the molecules is also decided by hybridization. It is expressed as,

  • For carbon and nitrogen with “sp” hybridization it is “linear”.
  • For carbon and nitrogen with “sp2” hybridization it is “trigonal planar”.
  • For carbon and nitrogen with “sp3” hybridization the geometry is “tetrahedral” and “pyramidal” respectively.

3.

Interpretation Introduction

To draw: The three-dimensional representations of the given compounds with the representation of wedge and dashed lines.

Interpretation: The three-dimensional diagrams of the given compounds with the representation of wedge and dashed lines are to be drawn.

Concept introduction: The three-dimensional representation of the molecule is described by the type of hybridization present in the molecule. On the basis of hybridization the bonding and non-bonding electrons are calculated. The bonding electrons are represented by single, double or triple bonds. The non-bonding electrons are represented by lone pairs of electron.

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Chapter 1 Solutions

Organic Chemistry (9th Edition)

Ch. 1.10A - Draw complete Lewis structures for the following...Ch. 1.10B - Give Lewis structures corresponding to the...Ch. 1.10B - Prob. 1.13PCh. 1.11 - Compute the empirical and molecular formulas for...Ch. 1.16 - a. Use your molecular models to make ethane, and...Ch. 1.17 - a. Predict the hybridization of the oxygen atom in...Ch. 1.17 - Predict the hybridization geometry and bond angles...Ch. 1.17 - Predict the hybridization, geometry, and bond...Ch. 1.17 - Prob. 1.19PCh. 1.17 - Allene, CH2=C=CH2, has the structure shown below...Ch. 1.17 - 1. Draw the important resonance forms for each...Ch. 1.18B - Prob. 1.22PCh. 1.18B - Two compounds with the formula CH3CH=NCH3 are...Ch. 1.19B - Prob. 1.24PCh. 1.19B - Give the relationship between the following pairs...Ch. 1 - a. Draw the resonance forms for SO2 (bonded OSO)....Ch. 1 - Name the element that corresponds to each...Ch. 1 - Prob. 1.28SPCh. 1 - For each compound, state whether its bonding is...Ch. 1 - a. Both PCl3 and PCl5 are stable compounds Draw...Ch. 1 - Draw a Lewis structure for each species a. N2H4 b....Ch. 1 - Prob. 1.32SPCh. 1 - Prob. 1.33SPCh. 1 - Draw Lewis structures for a. two compounds of...Ch. 1 - Prob. 1.35SPCh. 1 - Some of the following molecular formulas...Ch. 1 - Prob. 1.37SPCh. 1 - Give the molecular formula of each compound shown...Ch. 1 - 1. From what you remember of electronegativities,...Ch. 1 - For each of the following structures, 1. Draw a...Ch. 1 - Prob. 1.41SPCh. 1 - Prob. 1.42SPCh. 1 - Prob. 1.43SPCh. 1 - Prob. 1.44SPCh. 1 - For each pair of ions, determine which on is more...Ch. 1 - Use resonance structures to identify the areas of...Ch. 1 - Prob. 1.47SPCh. 1 - In 1934, Edward A. Doisy of Washington University...Ch. 1 - If the carbon atom in CH2Cl2 were fat. there would...Ch. 1 - Cyclopropane (C3H6, a three-membered ring) is more...Ch. 1 - Prob. 1.51SPCh. 1 - Prob. 1.52SPCh. 1 - In most amines, the nitrogen atom is sp3...Ch. 1 - Predict the hybridization and geometry of the...Ch. 1 - Draw orbital pictures of the pi bonding in the...Ch. 1 - Prob. 1.56SPCh. 1 - Prob. 1.57SPCh. 1 - Which of the following compounds show cis-trans...Ch. 1 - Give the relationships between the following pairs...Ch. 1 - Dimethyl sulfoxide (DMSO) has been used as an...
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