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Organic chemistry / John McMurry.

By: Material type: TextTextPublication details: [Pacific Grove, Calif.?] : Brooks/Cole Cengage Learning, c2012.Edition: 8th ed., International edDescription: 1 v. (various pagings) : ill. (chiefly col.) ; 26 cmISBN:
  • 9780840054531 (pbk.) :
  • 9780840054531 (Paper)
Subject(s): DDC classification:
  • 547 MCM
LOC classification:
  • QD251.3
Contents:
1.Structure and bonding -- 2.Polar covalent bonds; acids and bases -- 3.Organic compounds: alkanes and their stereochemistry -- 4.Organic compounds: cycloalkanes and their stereochemistry -- 5.Stereochemistry at tetrahedral centers -- 6.An overview of organic reactions -- 7.Alkenes: structure and reactivity -- 8.Alkenes: reactions and synthesis -- 9.Alkynes: an introduction to organic synthesis -- 10.Organohalides -- 11.Reactions of alkyl halides: nucleophilic substitutions and eliminiations -- 12.Structure determination: mass spectometry and infrared spectrosocpy -- 13.Structure determination: nuclear magnetic resonance spectrscopy -- 14.Conjugated compounds and ultraviolet spectroscopy -- 15.Benzene and aromaticity -- 16.Chemistry of benzene: electrophilic aromatic substitution -- 17.Alcohols and phenols -- 18.Ethers and expoxides; thiols and sulfides (preview of carbonyl chemistry) -- 19.Aldehydes and ketones: nucleophilic addition reactions -- 20.Carboxylic acids and nitriles -- 21.Carboxylic acid derivatives: nucleophilic acyl substitution reactions -- 22.Carbonyl alpha-substition reactios -- 23.Carbonyl condensation reactions -- 24.Amines and heterocytes -- 25.Biomolecules: carbohydrates -- 26.Biomolecules: amino acides, peptdies, and proteins -- 27.Biomolecules: lipids -- 28.Biomoledules: nucleic acids -- 29.The organic chemistry of metabolic pathways -- 30.Orbitals and organic chemistry: pericyclic reactions -- 31.Synthetic polymers.
Summary: Updated with the latest developments in the field, this book features accessible text which speaks to the needs of instructors and students.
Holdings
Item type Current library Call number Copy number Status Date due Barcode
Long Loan TUS: Midlands, Main Library Athlone Nursing Collection 547 MCM (Browse shelf(Opens below)) 1 Available 215935
Long Loan TUS: Midlands, Main Library Athlone Nursing Collection 547 MCM (Browse shelf(Opens below)) 1 Available 215934
Long Loan TUS: Midlands, Main Library Athlone General Lending 547 MCM (Browse shelf(Opens below)) 5463 Available 00213793

Previous ed.: 2008.

Ill. and text on inside covers.

Includes index.

Includes index.

1.Structure and bonding -- 2.Polar covalent bonds; acids and bases -- 3.Organic compounds: alkanes and their stereochemistry -- 4.Organic compounds: cycloalkanes and their stereochemistry -- 5.Stereochemistry at tetrahedral centers -- 6.An overview of organic reactions -- 7.Alkenes: structure and reactivity -- 8.Alkenes: reactions and synthesis -- 9.Alkynes: an introduction to organic synthesis -- 10.Organohalides -- 11.Reactions of alkyl halides: nucleophilic substitutions and eliminiations -- 12.Structure determination: mass spectometry and infrared spectrosocpy -- 13.Structure determination: nuclear magnetic resonance spectrscopy -- 14.Conjugated compounds and ultraviolet spectroscopy -- 15.Benzene and aromaticity -- 16.Chemistry of benzene: electrophilic aromatic substitution -- 17.Alcohols and phenols -- 18.Ethers and expoxides; thiols and sulfides (preview of carbonyl chemistry) -- 19.Aldehydes and ketones: nucleophilic addition reactions -- 20.Carboxylic acids and nitriles -- 21.Carboxylic acid derivatives: nucleophilic acyl substitution reactions -- 22.Carbonyl alpha-substition reactios -- 23.Carbonyl condensation reactions -- 24.Amines and heterocytes -- 25.Biomolecules: carbohydrates -- 26.Biomolecules: amino acides, peptdies, and proteins -- 27.Biomolecules: lipids -- 28.Biomoledules: nucleic acids -- 29.The organic chemistry of metabolic pathways -- 30.Orbitals and organic chemistry: pericyclic reactions -- 31.Synthetic polymers.

Updated with the latest developments in the field, this book features accessible text which speaks to the needs of instructors and students.

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