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The Resource Barron's E-Z organic chemistry, Bruce A. Hathaway

Barron's E-Z organic chemistry, Bruce A. Hathaway

Label
Barron's E-Z organic chemistry
Title
Barron's E-Z organic chemistry
Statement of responsibility
Bruce A. Hathaway
Title variation
E-Z organic chemistry
Creator
Contributor
Subject
Genre
Language
eng
Summary
Rev. ed. of: Organic chemistry the easy way. c2006
Cataloging source
DLC
http://library.link/vocab/creatorName
Hathaway, Bruce A
Dewey number
547
Illustrations
illustrations
Index
index present
LC call number
QD257
LC item number
.H38 2011
Literary form
non fiction
http://library.link/vocab/relatedWorkOrContributorName
Hathaway, Bruce A
http://library.link/vocab/subjectName
  • Chemistry, Organic
  • Chemistry, Organic
  • Chemistry, Organic
  • Organic chemistry
  • Organic chemistry
Label
Barron's E-Z organic chemistry, Bruce A. Hathaway
Link
http://catdir.loc.gov/catdir/enhancements/fy1116/2011000113-d.html
Instantiates
Publication
Note
  • Revised edition of: Organic chemistry the easy way. c2006
  • Includes index
Carrier category
volume
Carrier category code
nc
Carrier MARC source
rdacarrier
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Contents
  • 1. Important concepts that underlie most of organic chemistry -- Electronegativity -- Ionic and covalent bonding -- Writing chemical structures -- Isomerism -- Resonance -- Hydrogen-bonding and boiling points -- Water-solubility -- Acid-base concepts -- Functional groups
  • 2. Alkanes -- Structure and bonding -- IUPAC nomenclature -- Shapes of simple alkanes -- Shapes of cyclic alkanes -- Physical properties of alkanes
  • 3. Stereochemistry -- Stereogenic atoms -- Naming molecules with stereogenic atoms: The R, S (Cahn-Ingold-Prelog) System -- Possible relationships between two structures with the same molecular formula -- Optical rotation -- Implications of stereoisomerism
  • 4. Alkenes -- Structure and bonding -- IUPAC nomenclature -- Physical properties -- The general reaction of alkenes: addition to the C=C -- Introduction to reaction mechanisms -- Addition reactions of alkenes, classified by mechanistic similarities -- Diels-Alder reaction -- Preparations of alkenes
  • 5. Alkynes -- Structure and bonding -- IUPAC nomenclature -- The general reaction of alkynes: addition to the C=C -- Additions of H-X and water -- Addition of X2 -- Hydroboration -- Oxidation of alkynes with KMnO4 and ozone -- Reduction -- Acidity of 1-alkynes -- Preparations of alkynes
  • 6. Nucleophilic substitution and elimination reactions -- Base strength and nucleophile strength in water and hydrogen-bonding solvents -- Base strength and nucleophile strength in other solvents -- Reactions of methyl and primary alkyl halides with strong nucleophiles / bases -- Reactions of tertiary alkyl halides with strong nucleophiles / bases -- Reactions of secondary alkyl halides with strong nucleophiles / bases -- Reactions of tertiary alkyl halides with weak nucleophiles / bases -- Reactions of secondary alkyl halides with weak nucleophiles / bases -- Reactions of methyl and primary alkyl halides with weak nucleophiles / bases -- Carbocation rearrangements -- Summary of nucleophilic substitution and elimination reactions
  • 7. Free-radical reactions -- Introduction to free-radicals -- Free-radical chlorination of methane -- The energetics of halogenation of methane with other halogens -- Free-radical chlorination of other alkanes -- Free-radical bromination of alkanes -- The selectivity of free-radical bromination versus chlorination -- Other halogenating agents -- Free-radical halogenation of allylic and benzylic hydrogens -- Oxygen as a free-radical
  • 8. Alcohols and thiols -- IUPAC nomenclature of alcohols -- Physical properties of alcohols -- Reactions that cleave the O-H bond -- Reactions that cleave the C-O bond -- Oxidation of alcohols -- Preparations of alcohols -- Thiol naming and properties -- Thiol reactions and preparations
  • 9. Ethers, thioethers, and epoxides -- Structure and nomenclature -- Physical properties -- Preparations -- Reactions
  • 10. Aromatic compounds -- Structure of benzene -- Unexpected stability of benzene -- Hückel's rules -- Aromatic and antiaromatic compounds -- Nomenclature of benzene derivatives -- Electrophilic aromatic substitution of benzene -- Electrophilic aromatic substitution of substituted benzenes: directing abilities -- Electrophilic aromatic substitution of substituted benzenes: activating or deactivating effects -- Synthesis of disubstituted and trisubstituted benzenes -- Phenol naming and properties -- Other aromatic compounds
  • 11. Amines -- Nomenclature -- Physical properties -- Basicity -- Reactions as nucleophiles -- Reactions of amines with nitrous acid -- Preparations
  • 12. Aldehydes and ketones -- Nomenclature -- Physical properties -- General reaction: nucleophilic addition to the C=O -- Reactions with strong nucleophiles -- Reactions with weak nucleophiles -- Oxidations of aldehydes -- Reductions of aldehydes and ketones -- Preparations -- Acidity of the alpha-hydrogen -- Halogenation at the alpha-carbon -- Aldol condensation
  • 13. Carboxylic acids and derivatives -- Structures -- Nomenclature of carboxylic acids -- Physical properties of carboxylic acids -- Acidity of carboxylic acids -- The general reaction of carboxylic acid derivatives: nucleophilic acyl substitution, addition-elimination, or "up, down, and out" -- Conversions of carboxylic acids into carboxylic acid derivatives -- Naming of carboxylic acid derivatives -- Interconversions of carboxylic acids and derivatives -- Reductions of carboxylic acids and derivatives
  • 14. More chemistry of enols and enolates -- Acidities of various types of C-H bonds -- Alkylation of malonic esters and acetoacetic esters -- The Knoevenagel Condensation -- The Claisen Condensation and related reactions -- Conjugate addition reactions (The Michael Reaction) -- Robinson Annelation -- Alkylations and acylations of ketones
  • 15. Spectroscopy -- Infrared spectroscopy -- Nuclear magnetic resonance spectroscopy -- Mass spectrometry -- Putting it all together to solve problems
Control code
ocn700205484
Dimensions
26 cm
Extent
viii, 432 pages
Isbn
9780764144677
Lccn
2011000113
Media category
unmediated
Media MARC source
rdamedia
Media type code
n
Other physical details
illustrations
System control number
(OCoLC)700205484
Label
Barron's E-Z organic chemistry, Bruce A. Hathaway
Link
http://catdir.loc.gov/catdir/enhancements/fy1116/2011000113-d.html
Publication
Note
  • Revised edition of: Organic chemistry the easy way. c2006
  • Includes index
Carrier category
volume
Carrier category code
nc
Carrier MARC source
rdacarrier
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Contents
  • 1. Important concepts that underlie most of organic chemistry -- Electronegativity -- Ionic and covalent bonding -- Writing chemical structures -- Isomerism -- Resonance -- Hydrogen-bonding and boiling points -- Water-solubility -- Acid-base concepts -- Functional groups
  • 2. Alkanes -- Structure and bonding -- IUPAC nomenclature -- Shapes of simple alkanes -- Shapes of cyclic alkanes -- Physical properties of alkanes
  • 3. Stereochemistry -- Stereogenic atoms -- Naming molecules with stereogenic atoms: The R, S (Cahn-Ingold-Prelog) System -- Possible relationships between two structures with the same molecular formula -- Optical rotation -- Implications of stereoisomerism
  • 4. Alkenes -- Structure and bonding -- IUPAC nomenclature -- Physical properties -- The general reaction of alkenes: addition to the C=C -- Introduction to reaction mechanisms -- Addition reactions of alkenes, classified by mechanistic similarities -- Diels-Alder reaction -- Preparations of alkenes
  • 5. Alkynes -- Structure and bonding -- IUPAC nomenclature -- The general reaction of alkynes: addition to the C=C -- Additions of H-X and water -- Addition of X2 -- Hydroboration -- Oxidation of alkynes with KMnO4 and ozone -- Reduction -- Acidity of 1-alkynes -- Preparations of alkynes
  • 6. Nucleophilic substitution and elimination reactions -- Base strength and nucleophile strength in water and hydrogen-bonding solvents -- Base strength and nucleophile strength in other solvents -- Reactions of methyl and primary alkyl halides with strong nucleophiles / bases -- Reactions of tertiary alkyl halides with strong nucleophiles / bases -- Reactions of secondary alkyl halides with strong nucleophiles / bases -- Reactions of tertiary alkyl halides with weak nucleophiles / bases -- Reactions of secondary alkyl halides with weak nucleophiles / bases -- Reactions of methyl and primary alkyl halides with weak nucleophiles / bases -- Carbocation rearrangements -- Summary of nucleophilic substitution and elimination reactions
  • 7. Free-radical reactions -- Introduction to free-radicals -- Free-radical chlorination of methane -- The energetics of halogenation of methane with other halogens -- Free-radical chlorination of other alkanes -- Free-radical bromination of alkanes -- The selectivity of free-radical bromination versus chlorination -- Other halogenating agents -- Free-radical halogenation of allylic and benzylic hydrogens -- Oxygen as a free-radical
  • 8. Alcohols and thiols -- IUPAC nomenclature of alcohols -- Physical properties of alcohols -- Reactions that cleave the O-H bond -- Reactions that cleave the C-O bond -- Oxidation of alcohols -- Preparations of alcohols -- Thiol naming and properties -- Thiol reactions and preparations
  • 9. Ethers, thioethers, and epoxides -- Structure and nomenclature -- Physical properties -- Preparations -- Reactions
  • 10. Aromatic compounds -- Structure of benzene -- Unexpected stability of benzene -- Hückel's rules -- Aromatic and antiaromatic compounds -- Nomenclature of benzene derivatives -- Electrophilic aromatic substitution of benzene -- Electrophilic aromatic substitution of substituted benzenes: directing abilities -- Electrophilic aromatic substitution of substituted benzenes: activating or deactivating effects -- Synthesis of disubstituted and trisubstituted benzenes -- Phenol naming and properties -- Other aromatic compounds
  • 11. Amines -- Nomenclature -- Physical properties -- Basicity -- Reactions as nucleophiles -- Reactions of amines with nitrous acid -- Preparations
  • 12. Aldehydes and ketones -- Nomenclature -- Physical properties -- General reaction: nucleophilic addition to the C=O -- Reactions with strong nucleophiles -- Reactions with weak nucleophiles -- Oxidations of aldehydes -- Reductions of aldehydes and ketones -- Preparations -- Acidity of the alpha-hydrogen -- Halogenation at the alpha-carbon -- Aldol condensation
  • 13. Carboxylic acids and derivatives -- Structures -- Nomenclature of carboxylic acids -- Physical properties of carboxylic acids -- Acidity of carboxylic acids -- The general reaction of carboxylic acid derivatives: nucleophilic acyl substitution, addition-elimination, or "up, down, and out" -- Conversions of carboxylic acids into carboxylic acid derivatives -- Naming of carboxylic acid derivatives -- Interconversions of carboxylic acids and derivatives -- Reductions of carboxylic acids and derivatives
  • 14. More chemistry of enols and enolates -- Acidities of various types of C-H bonds -- Alkylation of malonic esters and acetoacetic esters -- The Knoevenagel Condensation -- The Claisen Condensation and related reactions -- Conjugate addition reactions (The Michael Reaction) -- Robinson Annelation -- Alkylations and acylations of ketones
  • 15. Spectroscopy -- Infrared spectroscopy -- Nuclear magnetic resonance spectroscopy -- Mass spectrometry -- Putting it all together to solve problems
Control code
ocn700205484
Dimensions
26 cm
Extent
viii, 432 pages
Isbn
9780764144677
Lccn
2011000113
Media category
unmediated
Media MARC source
rdamedia
Media type code
n
Other physical details
illustrations
System control number
(OCoLC)700205484

Library Locations

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      585 Liberty Street SE, Salem, OR, 97301, US
      44.934972 -123.041775
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