Concept explainers
a) CHCl3, chloroform
Interpretation:
The line – bond structure, showing all nonbonding electrons for CHCl3, chloroform is to be given.
Concept introduction:
A covalent bond is formed by mutual sharing of two electrons between the atoms, each atom giving one electron for sharing. Such a covalent bond, that is, a pair of shared electrons is represented as a line between the atoms, for example as A-B. Valence electrons that are not used for bonding are called lone-pair of electrons or nonbonding electrons. The nonbonding electrons are usually omitted while drawing line-bond structure.
To determine:
The line – bond structure, showing all nonbonding electrons for CHCl3, chloroform
b) CH3NH2, methylamine
Interpretation:
The line – bond structure, showing all nonbonding electrons for CH3NH2, methylamine is to be given.
Concept introduction:
A covalent bond is formed by mutual sharing of two electrons between the atoms, each atom giving one electron for sharing. Such a covalent bond, that is, a pair of shared electrons is represented as a line between the atoms, for example as A-B. Valence electrons that are not used for bonding are called lone-pair of electrons or nonbonding electrons. The nonbonding electrons are usually omitted while drawing line-bond structure.
To determine:
The line – bond structure, showing all nonbonding electrons for CH3NH2, methylamine.
c) H2S, hydrogen sulfide
Interpretation:
The line – bond structure, showing all nonbonding electrons for H2S, hydrogen sulfide is to be given.
Concept introduction:
A covalent bond is formed by mutual sharing of two electrons between the atoms, each atom giving one electron for sharing. Such a covalent bond, that is, a pair of shared electrons is represented as a line between the atoms, for example as A-B. Valence electrons that are not used for bonding are called lone-pair of electrons or nonbonding electrons. The nonbonding electrons are usually omitted while drawing line-bond structure.
To determine:
The line – bond structure, showing all nonbonding electrons for H2S, hydrogen sulfide.
d) CH3 Li, methyllithium
Interpretation:
The line – bond structure, showing all nonbonding electrons for CH3 Li, methyllithium is to be given.
Concept introduction:
A covalent bond is formed by mutual sharing of two electrons between the atoms, each atom giving one electron for sharing. Such a covalent bond, that is, a pair of shared electrons is represented as a line between the atoms, for example as A-B. Valence electrons that are not used for bonding are called lone-pair of electrons or nonbonding electrons. The nonbonding electrons are usually omitted while drawing line-bond structure.
To determine:
The line – bond structure, showing all nonbonding electrons for CH3 Li, methyllithium
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Chapter 1 Solutions
OWLv2 with Student Solutions Manual eBook, 4 terms (24 months) Printed Access Card for McMurry's Organic Chemistry, 9th
- H-Br Energy 1) Draw the step-by-step mechanism by which 3-methylbut-1-ene is converted into 2-bromo-2-methylbutane. 2) Sketch a reaction coordinate diagram that shows how the internal energy (Y- axis) of the reacting species change from reactants to intermediate(s) to product. Brarrow_forward2. Draw the missing structure(s) in each of the following reactions. The missing structure(s) can be a starting material or the major reaction product(s). C5H10 H-CI CH2Cl2 CIarrow_forwardDraw the products of the stronger acid protonating the other reactant. དའི་སྐད”“ H3C OH H3C CH CH3 KEq Product acid Product basearrow_forward
- Draw the products of the stronger acid protonating the other reactant. H3C NH2 NH2 KEq H3C-CH₂ 1. Product acid Product basearrow_forwardWhat alkene or alkyne yields the following products after oxidative cleavage with ozone? Click the "draw structure" button to launch the drawing utility. draw structure ... andarrow_forwardDraw the products of the stronger acid protonating the other reactant. H3C-C=C-4 NH2 KEq CH H3C `CH3 Product acid Product basearrow_forward
- 2. Draw the missing structure(s) in each of the following reactions. The missing structure(s) can be a starting material or the major reaction product(s). C5H10 Br H-Br CH2Cl2 + enant.arrow_forwardDraw the products of the stronger acid protonating the other reactant. KEq H₂C-O-H H3C OH Product acid Product basearrow_forwardDraw the products of the stronger acid protonating the other reactant. OH KEq CH H3C H3C `CH3 Product acid Product basearrow_forward
- 2. Draw the missing structure(s) in each of the following reactions. The missing structure(s) can be a starting material or the major reaction product(s). Ph H-I CH2Cl2arrow_forward3 attempts left Check my work Draw the products formed in the following oxidative cleavage. [1] 03 [2] H₂O draw structure ... lower mass product draw structure ... higher mass productarrow_forward2. Draw the missing structure(s) in each of the following reactions. The missing structure(s) can be a starting material or the major reaction product(s). H-Br CH2Cl2arrow_forward
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning