Organic Chemistry
Organic Chemistry
8th Edition
ISBN: 9781305580350
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
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Chapter 1.5, Problem 1.14P

(a)

Interpretation Introduction

Interpretation:

Polar molecules and the direction of its dipole moment have to be identified.

Concept introduction:

Polar Molecules:

Polar Molecules contains partial positive and partial negative charge in the molecule due its electronegativity difference between the molecules.

Dipole moment:

The charge separation of the molecule produces dipole moment. Dipole moment arises between two ions in an ionic bond or covalent bond.

Dipole moment depends on the differences in electronegativity of the atom in the molecule. The electronegativity is more, the larger the dipole moment. The dipole moment is calculated from the polarity of the molecule.

(b)

Interpretation Introduction

Interpretation:

Polar molecules and the direction of its dipole moment have to be identified.

Concept introduction:

Polar Molecules:

Polar Molecules contains partial positive and partial negative charge in the molecule due its electronegativity difference between the molecules.

Dipole moment:

The charge separation of the molecule produces dipole moment. Dipole moment arises between two ions in an ionic bond or covalent bond.

Dipole moment depends on the differences in electronegativity of the atom in the molecule. The electronegativity is more, the larger the dipole moment. The dipole moment is calculated from the polarity of the molecule.

(c)

Interpretation Introduction

Interpretation:

Polar molecules and the direction of its dipole moment have to be identified.

Concept introduction:

Polar Molecules:

Polar Molecules contains partial positive and partial negative charge in the molecule due its electronegativity difference between the molecules.

Dipole moment:

The charge separation of the molecule produces dipole moment. Dipole moment arises between two ions in an ionic bond or covalent bond.

Dipole moment depends on the differences in electronegativity of the atom in the molecule. The electronegativity is more, the larger the dipole moment. The dipole moment is calculated from the polarity of the molecule.

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Draw a Lewis structure for each of the following molecules: (a) chlorodifluoromethane, CHClF2 (b) propanoic acid, C2 H5CO2H (basic structure pictured below) (c) acetonitrile, CH3CH (the framework is H3C-C-N) (d) allene, H3CCCH2
The structural formulas for ethanol, CH3CH2OH, and propene, CH;CH=CH,2, are нн H Н—С—С—0—н H-C-C=C-H нн H H H Ethanol Propene (a) Complete the Lewis structure for each molecule showing all valence electrons. (b) Using the VSEPR model, predict all bond angles in each molecule.
Draw a Lewis structure for each of the following                                        molecule:                                                     (a) chlorodifluoromethane, CHCIF2                                                               (b) propanoic acid C2H5CO2H (basic structure                                                  pictured below)                                                                                                                                                                                                                                                                                                                                                                                                                                                              (c) acetonitrile, CH3CN ( the framework is H3C-C-N)                                     (d) allene, H2CCCH2

Chapter 1 Solutions

Organic Chemistry

Ch. 1.3 - Prob. 1.11PCh. 1.3 - Prob. 1.12PCh. 1.4 - Predict all bond angles for these molecules. (a)...Ch. 1.5 - The geometry of carbon in diamond is tetrahedral,...Ch. 1.5 - Because of their spherical shape, C60 molecules...Ch. 1.5 - What best describes the CCC bond angles in C60? 1....Ch. 1.5 - Prob. 1.14PCh. 1.7 - Describe the bonding in these molecules in terms...Ch. 1.8 - Prob. 1.16PCh. 1.8 - Prob. 1.17PCh. 1.8 - Prob. 1.18PCh. 1.9 - Draw three contributing structures of the...Ch. 1.9 - What is the hybridization state of the circled...Ch. 1.9 - The molecule shown on the right in the example in...Ch. 1.9 - Prob. CQCh. 1.9 - The following structure is called imidazolium....Ch. 1 - Write the ground-state electron configuration for...Ch. 1 - Identify the atom that has each ground-state...Ch. 1 - Define valence shell and valence electron.Ch. 1 - How many electrons are in the valence shell of...Ch. 1 - Prob. 1.24PCh. 1 - Prob. 1.25PCh. 1 - Prob. 1.26PCh. 1 - Write Lewis structures for these compounds. Show...Ch. 1 - Write Lewis structures for these ions. Show all...Ch. 1 - Prob. 1.29PCh. 1 - Some of these structural formulas are incorrect...Ch. 1 - Following the rule that each atom of carbon,...Ch. 1 - Following are several Lewis structures showing all...Ch. 1 - Which statements are true about electronegativity?...Ch. 1 - Why does fluorine, the element in the upper right...Ch. 1 - Arrange the single covalent bonds within each set...Ch. 1 - Using the values of electronegativity given in...Ch. 1 - Prob. 1.37PCh. 1 - Use VSEPR to predict bond angles about each...Ch. 1 - Use VSEPR to predict bond angles about each atom...Ch. 1 - Use VSEPR to predict the geometry of these ions....Ch. 1 - Prob. 1.41PCh. 1 - Prob. 1.42PCh. 1 - What is the meaning of the term tertiary (3) when...Ch. 1 - What is the meaning of the term tertiary (3) when...Ch. 1 - Draw structural formulas for (a) The four primary...Ch. 1 - Draw structural formulas for the three tertiary...Ch. 1 - Prob. 1.47PCh. 1 - Identify the functional groups in each compound.Ch. 1 - Draw a three-dimensional representation for each...Ch. 1 - Tetrafluoroethylene, C2F4, is the starting...Ch. 1 - Which statements are true about resonance...Ch. 1 - Prob. 1.52PCh. 1 - Prob. 1.53PCh. 1 - Prob. 1.54PCh. 1 - Are the structures in each set valid contributing...Ch. 1 - State the orbital hybridization of each...Ch. 1 - Describe each highlighted bond in terms of the...Ch. 1 - Following is a structural formula of the...Ch. 1 - Draw a Lewis structure for methyl isocyanate,...Ch. 1 - What is the hybridization of the highlighted atoms...Ch. 1 - Using cartoon representations, draw a molecular...Ch. 1 - In what kind of orbitals do the lone-pair...Ch. 1 - Draw the delocalized molecular orbitals for the...Ch. 1 - Prob. 1.64APCh. 1 - Each compound contains both ions and covalent...Ch. 1 - Predict whether the carbon-metal bond in these...Ch. 1 - Prob. 1.67APCh. 1 - Phosphorus is immediately under nitrogen in the...Ch. 1 - Draw a Lewis structure for the azide ion, N3. (The...Ch. 1 - Cyanic acid, HOCN, and isocyanic acid, HNCO,...Ch. 1 - In Chapter 6, we study a group of organic cations...Ch. 1 - Many reactions involve a change in hybridization...Ch. 1 - Following is a structural formula of benzene,...Ch. 1 - Following are three contributing structures for...Ch. 1 - (a) Draw a Lewis structure for the ozone molecule,...Ch. 1 - The following two compounds are isomers; that is,...Ch. 1 - In future chapters, we will encounter...Ch. 1 - Prob. 1.78AP
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