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Organic Chemistry: A Guided Inquiry (Moog/Spencer Guided Inquiry Course)
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- Buy It NowOrganic Chemistry: A Guided Inquiry (Moog/Spencer Guided Inquiry Course)
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Located in: Lookout Mountain, Georgia, United States
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Seller assumes all responsibility for this listing.
eBay item number:391965832446
Item specifics
- Condition
- Artist
- Straumanis, Andrei
- ISBN
- 9780618308521
- Subject Area
- Education, Science
- Publication Name
- Organic Chemistry : a Guided Inquiry
- Item Length
- 10.9 in
- Publisher
- Cengage Learning
- Subject
- General, Chemistry / Organic
- Publication Year
- 2003
- Type
- Textbook
- Format
- Trade Paperback
- Language
- English
- Item Height
- 0.6 in
- Item Width
- 8.4 in
- Item Weight
- 32.1 Oz
- Number of Pages
- 448 Pages
About this product
Product Information
Designed to encourage active and collaborative learning in the organic chemistry classroom, this text is a collection of group activities (ChemActivities) that can accompany any organic chemistry text. These ChemActivities teach students how to think like scientists, rather than simply memorizing important conclusions arrived at by great scientists of the past.
Product Identifiers
Publisher
Cengage Learning
ISBN-10
0618308520
ISBN-13
9780618308521
eBay Product ID (ePID)
102822073
Product Key Features
Publication Name
Organic Chemistry : a Guided Inquiry
Format
Trade Paperback
Language
English
Subject
General, Chemistry / Organic
Publication Year
2003
Type
Textbook
Subject Area
Education, Science
Number of Pages
448 Pages
Dimensions
Item Length
10.9 in
Item Height
0.6 in
Item Width
8.4 in
Item Weight
32.1 Oz
Additional Product Features
LCCN
2003-274303
Lc Classification Number
Qd257.S77 2004
Reviews
ChemActivity 1Part A: Bond AnglesPart B: Molecular ShapeChemActivity 2Part A: Lewis StructuresPart B: Formal ChargeChemActivity 3Part A: Resonance StructuresPart B: Curved Arrow NotationChemActivity 4Conformers of Carbon StructuresChemActivity 5Part A: Constitutional IsomersPart B: StereoisomersChemActivity 6Part A: Energy DiagramsPart B: Cyclohexane ConformationsChemActivity 7Part A: ChiralityPart B: Absolute ConfigurationChemActivity 8Acid-Base ReactionsChemActivity 9Part A: The Core Change EffectPart B: The Inductive EffectChemActivity 10Resonance EffectsChemActivity 11Part A: Orbitals and Sigma BondsPart B: Orbitals and Pi BondsChemActivity 12Part A: One-Step Nucleophilic SubstitutionPart B: One-Step Nucleophilic SubstitutionChemActivity 13Part A: CarbocationsPart B: Two-Step Nucleophilic Substitution ReactionsChemActivity 14Part A: Two-Step EliminationPart B: One-Step EliminationChemActivity 15Part A: Alkene Potential EnergyPart B: Stereochemistry of E2 ReactionsChemActivity 16Spectroscopy Part A: IRSpectroscopy Part B: 13C NMRSpectroscopy Part C: 1H NMRChemActivity 17Part A: Electrophilic AdditionPart B: Carbocation RearrangementsPart C: Acid Catalyzed Electrophilic AdditionPart D: Electrophilic Addition to a DieneChemActivity 18Epoxide & Bromonium Ring OpeningChemActivity 19Carbon-Carbon Bond FormationChemActivity 20Part A: Radical Halogenation ReactionsPart B: Radical Chain ReactionsChemActivity 21Anti-Markovnikov Addition of H-BrChemActivity 22Part A: Hydroboration/OxidationPart B: Other Oxidation ReactionsChemActivity 23Electrophilic Addition to AlkynesChemActivity 24Part A: Conjugated Double BondsPart B: Molecular Orbital TheoryChemActivity 25Part A: AromaticityPart B: MO Explanation for AromaticityChemActivity 26NMR of Aromatic MoleculesChemActivity 27Polymerization ReactionsChemActivity 28Diels-Alder Cylcloaddition ReactionsChemActivity 29Part A: Electrophilic Aromatic SubstitutionPart B: Substituent EffectsPart C: Resonance Donating and Withdrawing GroupsPart D: Summary of Directing EffectsMini-Activity on Lewis Acid CatalysisChemActivity 30Synthesis Workshop IChemActivity 31Part A: Nucleophilic Addition to C=OPart B: Nucleophilic Addition-EliminationChemActivity 32Protecting GroupsChemActivity 33Part A: Acidity of the alpha-HydrogenPart B: Enol vs. EnolateChemActivity 34Part A: Aldol ReactionPart B: Mixed Aldol ReactionsPart C: "Condensation Reactions"ChemActivity 35Acid Catalyzed Aldol ReactionsChemActivity 36Part A: 1,4-Addition to alpha,beta-Unsaturated Carbonyl CompoundsPart B: Nucleophiles that Prefer 1,2-Addition to an alpha,beta-Unsaturated CarbonylChemActivity 37Michael AdditionChemActivity 38Part A: pKa of PhenolsPart B: pKa's of Substituted PhenolsChemActivity 39Nucleophilic Aromatic Substitution (NAS)ChemActivity 40Part A: Reactions of Carboxylic AcidsPart B: Reactions of Carboxylic AcidsChemActivity 41Part A: Reactions of Alkanoyl Chlorides (Acid Chlorides)Part B: Reactions of Acid AnhydridesChemActivity 42Part A: Claisen ReactionPart B: Mixed Claisen ReactionsPart C: Aldol vs. ClaisenChemActivity 43DecarboxylationChemActivity 44Synthesis Workshop IIChemActivity 45Part A: Basicity of AminesPart B: Synthesis of Amines/pKa of AA'sChemActivity 46Part A: Amino Acids and PeptidesPart B: ProteinsAppendix N: Nomenclature WorksheetsNomenclature Worksheet INomenclature Worksheet IIAppendix R: Reaction Summary SheetsPreparation/Reactions of Alkyl Halides and AlcoholsPreparation/Reactions of Ethers and AminesPreparation/Reactions of AlkenesOxidative Cleavage of Alkenes/Oxidation of AlcoholsPreparation/Reactions of AlkynesEAS and Aromatic Sidechain ReactionsPreparation/Reactions of Aldehydes and KetonesSpecial Reactions of Aldehydes and KetonesReactions of alpha-C NucleophilesPreparation/Reactions of Carboxylic AcidsPreparation/Reactions of Esters and AmidesNucleophilic Aromatic Substitution (NAS)Claisen ReactionSpecial Ketone SynthesisPreparation of Amines
Table of Content
ChemActivity 1Part A: Bond AnglesPart B: Molecular ShapeChemActivity 2Part A: Lewis StructuresPart B: Formal ChargeChemActivity 3Part A: Resonance StructuresPart B: Curved Arrow NotationChemActivity 4Conformers of Carbon StructuresChemActivity 5Part A: Constitutional IsomersPart B: StereoisomersChemActivity 6Part A: Energy DiagramsPart B: Cyclohexane ConformationsChemActivity 7Part A: ChiralityPart B: Absolute ConfigurationChemActivity 8Acid-Base ReactionsChemActivity 9Part A: The Core Change EffectPart B: The Inductive EffectChemActivity 10Resonance EffectsChemActivity 11Part A: Orbitals and Sigma BondsPart B: Orbitals and Pi BondsChemActivity 12Part A: One-Step Nucleophilic SubstitutionPart B: One-Step Nucleophilic SubstitutionChemActivity 13Part A: CarbocationsPart B: Two-Step Nucleophilic Substitution ReactionsChemActivity 14Part A: Two-Step EliminationPart B: One-Step EliminationChemActivity 15Part A: Alkene Potential EnergyPart B: Stereochemistry of E2 ReactionsChemActivity 16Spectroscopy Part A: IRSpectroscopy Part B: 13C NMRSpectroscopy Part C: 1H NMRChemActivity 17Part A: Electrophilic AdditionPart B: Carbocation RearrangementsPart C: Acid Catalyzed Electrophilic AdditionPart D: Electrophilic Addition to a DieneChemActivity 18Epoxide & Bromonium Ring OpeningChemActivity 19Carbon-Carbon Bond FormationChemActivity 20Part A: Radical Halogenation ReactionsPart B: Radical Chain ReactionsChemActivity 21Anti-Markovnikov Addition of H-BrChemActivity 22Part A: Hydroboration/OxidationPart B: Other Oxidation ReactionsChemActivity 23Electrophilic Addition to AlkynesChemActivity 24Part A: Conjugated Double BondsPart B: Molecular Orbital TheoryChemActivity 25Part A: AromaticityPart B: MO Explanation for AromaticityChemActivity 26NMR of Aromatic MoleculesChemActivity 27Polymerization ReactionsChemActivity 28Diels-Alder Cylcloaddition ReactionsChemActivity 29Part A: Electrophilic Aromatic SubstitutionPart B: Substituent EffectsPart C: Resonance Donating and Withdrawing GroupsPart D: Summary of Directing EffectsMini-Activity on Lewis Acid CatalysisChemActivity 30Synthesis Workshop IChemActivity 31Part A: Nucleophilic Addition to C=OPart B: Nucleophilic Addition-EliminationChemActivity 32Protecting GroupsChemActivity 33Part A: Acidity of the alpha-HydrogenPart B: Enol vs. EnolateChemActivity 34Part A: Aldol ReactionPart B: Mixed Aldol ReactionsPart C: "Condensation ReactionsChemActivity 35Acid Catalyzed Aldol ReactionsChemActivity 36Part A: 1,4-Addition to alpha,beta-Unsaturated Carbonyl CompoundsPart B: Nucleophiles that Prefer 1,2-Addition to an alpha,beta-Unsaturated CarbonylChemActivity 37Michael AdditionChemActivity 38Part A: pKa of PhenolsPart B: pKa's of Substituted PhenolsChemActivity 39Nucleophilic Aromatic Substitution (NAS)ChemActivity 40Part A: Reactions of Carboxylic AcidsPart B: Reactions of Carboxylic AcidsChemActivity 41Part A: Reactions of Alkanoyl Chlorides (Acid Chlorides)Part B: Reactions of Acid AnhydridesChemActivity 42Part A: Claisen ReactionPart B: Mixed Claisen ReactionsPart C: Aldol vs. ClaisenChemActivity 43DecarboxylationChemActivity 44Synthesis Workshop IIChemActivity 45Part A: Basicity of AminesPart B: Synthesis of Amines/pKa of AA'sChemActivity 46Part A: Amino Acids and PeptidesPart B: ProteinsAppendix N: Nomenclature WorksheetsNomenclature Worksheet INomenclature Worksheet IIAppendix R: Reaction Summary SheetsPreparation/Reactions of Alkyl Halides and AlcoholsPreparation/Reactions of Ethers and AminesPreparation/Reactions of AlkenesOxidative Cleavage of Alkenes/Oxidation of AlcoholsPreparation/Reactions of AlkynesEAS and Aromatic Sidechain ReactionsPreparation/Reactions of Aldehydes and KetonesSpecial Reactions of Aldehydes and KetonesReactions of alpha-C NucleophilesPreparation/Reactions of Carboxylic AcidsPreparation/Reactions of Esters and AmidesNucleophilic A
Copyright Date
2004
Target Audience
College Audience
Dewey Decimal
547
Dewey Edition
22
Illustrated
Yes
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eBay item number:391965832446
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