EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
9th Edition
ISBN: 9780100591318
Author: McMurry
Publisher: YUZU
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Chapter 1.SE, Problem 43AP
Interpretation Introduction

Interpretation:

To give the number of hydrogen atoms bonded to each carbon atom in the substance given, and to write its molecular formula.

Concept introduction:

In skeletal structures the carbon atoms are not usually shown. Instead a carbon is assumed to be at each intersection of two lines and at the end of each line. The hydrogen atoms bonded to carbons are also not shown. The correct number of hydrogen atoms for each carbon atom is assigned keeping in mind that carbon has a valence of 4. The end of a line represents a carbon atom with three hydrogen atoms, CH3; a two-way intersection is a carbon atom with two hydrogen atoms, CH2; a three way intersection is a carbon with one hydrogen, CH; a four way intersection is a carbon with no attached hydrogen. Atoms other than carbon and hydrogen are shown. The molecular formula can be obtained by counting the number of atoms of different elements present in the molecule.

To determine:

The number of hydrogen atoms bonded to each carbon atom in the substance given and to write its molecular formula.

Interpretation Introduction

Interpretation:

To give the number of hydrogen atoms bonded to each carbon atom in the substances given, and to write the molecular formula.

Concept introduction:

In skeletal structures the carbon atoms are not usually shown. Instead a carbon is assumed to be at each intersection of two lines and at the end of each line. The hydrogen atoms bonded to carbons are also not shown. The correct number of hydrogen atoms for each carbon atom is assigned keeping in mind that carbon has a valence of 4. The end of a line represents a carbon atom with three hydrogen atoms, CH3; a two-way intersection is a carbon atom with two hydrogen atoms, CH2; a three way intersection is a carbon with one hydrogen, CH; a four way intersection is a carbon with no attached hydrogen. Atoms other than carbon and hydrogen are shown. The molecular formula can be obtained by counting the number of atoms of different elements present in the molecule.

To determine:

The number of hydrogen atoms bonded to each carbon atom in the substance given, and to write its molecular formula.

Interpretation Introduction

Interpretation:

To give the number of hydrogen atoms bonded to each carbon atom in the substance given, and to write its molecular formula.

Concept introduction:

In skeletal structures the carbon atoms are not usually shown. Instead a carbon is assumed to be at each intersection of two lines and at the end of each line. The hydrogen atoms bonded to carbons are also not shown. The correct number of hydrogen atoms for each carbon atom is assigned keeping in mind that carbon has a valence of 4. The end of a line represents a carbon atom with three hydrogen atoms, CH3; a two-way intersection is a carbon atom with two hydrogen atoms, CH2; a three way intersection is a carbon with one hydrogen, CH; a four way intersection is a carbon with no attached hydrogen. Atoms other than carbon and hydrogen are shown. The molecular formula can be obtained by counting the number of atoms of different elements present in the molecule.

To determine:

The number of hydrogen atoms bonded to each carbon atom in the substance given, and to write its molecular formula.

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Chapter 1 Solutions

EBK ORGANIC CHEMISTRY

Ch. 1.8 - Draw a line-bond structure for 1, 3-butadiene,...Ch. 1.8 - Following is a molecular model of aspirin...Ch. 1.9 - Draw a line-bond structure for propyne, CH3C≡CH....Ch. 1.10 - Prob. 14PCh. 1.12 - Prob. 15PCh. 1.12 - Prob. 16PCh. 1.12 - The following molecular model is a representation...Ch. 1.SE - Convert each of the following molecular models...Ch. 1.SE - The following model is a representation of citric...Ch. 1.SE - The following model is a representation of...Ch. 1.SE - The following model is a representation of...Ch. 1.SE - How many valence electrons does each of the...Ch. 1.SE - Give the ground-state electron configuration for...Ch. 1.SE - Prob. 24APCh. 1.SE - Prob. 25APCh. 1.SE - Draw an electron-dot structure for acetonitrile,...Ch. 1.SE - Draw a line-bond structure for vinyl chloride,...Ch. 1.SE - Fill in any nonbonding valence electrons that are...Ch. 1.SE - Convert the following line-bond structures into...Ch. 1.SE - Convert the following molecular formulas into...Ch. 1.SE - Prob. 31APCh. 1.SE - Oxaloacetic acid, an important intermediate in...Ch. 1.SE - Prob. 33APCh. 1.SE - Potassium methoxide, KOCH3, contains both covalent...Ch. 1.SE - What is the hybridization of each carbon atom in...Ch. 1.SE - Prob. 36APCh. 1.SE - Prob. 37APCh. 1.SE - What bond angles do you expect for each of the...Ch. 1.SE - Propose structures for molecules that meet the...Ch. 1.SE - What kind of hybridization do you expect for each...Ch. 1.SE - Pyridoxal phosphate, a close relative of vitamin...Ch. 1.SE - Prob. 42APCh. 1.SE - Prob. 43APCh. 1.SE - Quetiapine, marketed as Seroquel, is a heavily...Ch. 1.SE - Tell the number of hydrogens bonded to each carbon...Ch. 1.SE - Why do you suppose no one has ever been able to...Ch. 1.SE - Allene, H2C=C=CH2, is somewhat unusual in that it...Ch. 1.SE - Allene (see Problem 1-47) is structurally related...Ch. 1.SE - Complete the electron-dot structure of caffeine,...Ch. 1.SE - Most stable organic species have tetravalent...Ch. 1.SE - A carbanion is a species that contains a...Ch. 1.SE - Divalent carbon species called carbenes are...Ch. 1.SE - There are two different substances with the...Ch. 1.SE - There are two different substances with the...Ch. 1.SE - There are two different substances with the...Ch. 1.SE - Prob. 56APCh. 1.SE - Among the most common over-the-counter drugs you...
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