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AR-BaUEN |
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130430s2012 enka|||f |||| 00| 0|eng|d |
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|a AR-BaUEN
|b spa
|c AR-BaUEN
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| 020 |
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|a 9780199270293
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| 044 |
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|a xxk
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| 080 |
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|a 547
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| 100 |
1 |
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|a Clayden, Jonathan
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| 245 |
1 |
0 |
|a Organic chemistry
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| 250 |
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|a 2nd. ed.
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| 260 |
|
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|a Oxford :
|b Oxford University Press,
|c 2012
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| 300 |
|
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|a xxv, 1234 p. :
|b il.
|
| 505 |
0 |
0 |
|t Abbreviations
|
| 505 |
0 |
0 |
|t Preface to the second edition
|
| 505 |
0 |
0 |
|t Organic chemistry and this book
|
| 505 |
0 |
0 |
|g 1
|t What is organic chemistry?
|
| 505 |
0 |
0 |
|g 2
|t Organic structures
|
| 505 |
0 |
0 |
|g 3
|t Determining organic structures
|
| 505 |
0 |
0 |
|g 4
|t Structures of molecules
|
| 505 |
0 |
0 |
|g 5
|t Organic reactions
|
| 505 |
0 |
0 |
|g 6
|t Nucleophilic addition to the carbonyl group
|
| 505 |
0 |
0 |
|g 7
|t Delocalization and conjugation
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| 505 |
0 |
0 |
|g 8
|t Acidity, basicity, and pKa
|
| 505 |
0 |
0 |
|g 9
|t Using organometallic reagents to make C-C bonds
|
| 505 |
0 |
0 |
|g 10
|t Nucleophilic substitution at the carbonyl group
|
| 505 |
0 |
0 |
|g 11
|t Nucleophilic substitution at C=O with loss of carbonyl oxygen
|
| 505 |
0 |
0 |
|g 12
|t Equilibria, rates, and mechanisms
|
| 505 |
0 |
0 |
|g 13
|t ¹H NMR: Proton nuclear magnetic resonance
|
| 505 |
0 |
0 |
|g 14
|t Stereochemistry
|
| 505 |
0 |
0 |
|g 15
|t Nucleophilic substitution at saturated carbon
|
| 505 |
0 |
0 |
|g 16
|t Conformational analysis
|
| 505 |
0 |
0 |
|g 17
|t Elimination reactions
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| 505 |
0 |
0 |
|g 18
|t Review of spectroscopic methods
|
| 505 |
0 |
0 |
|g 19
|t Electrophilic additions to alkenes
|
| 505 |
0 |
0 |
|g 20
|t Formation and reactions of enols and enolates
|
| 505 |
0 |
0 |
|g 21
|t Electrophilic aromatic substitution
|
| 505 |
0 |
0 |
|g 22
|t Conjugate addition and nucleophilic aromatic substitution
|
| 505 |
0 |
0 |
|g 23
|t Chemoselectivity and protecting groups
|
| 505 |
0 |
0 |
|g 24
|t Regioselectivity
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| 505 |
0 |
0 |
|g 25
|t Alkylation of enolates
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| 505 |
0 |
0 |
|g 26
|t Reactions of enolates with carbonyl compounds: the aldol and Claisen reactions
|
| 505 |
0 |
0 |
|g 27
|t Sulfur, silicon, and phosphorus in organic chemistry
|
| 505 |
0 |
0 |
|g 28
|t Retrosynthetic analysis
|
| 505 |
0 |
0 |
|g 29
|t Aromatic heterocycles 1: reactions
|
| 505 |
0 |
0 |
|g 30
|t Aromatic heterocycles 2: synthesis
|
| 505 |
0 |
0 |
|g 31
|t Saturated heterocycles and stereoelectronics
|
| 505 |
0 |
0 |
|g 32
|t Stereoselectivity in cyclic molecules
|
| 505 |
0 |
0 |
|g 33
|t Diastereoselectivity
|
| 505 |
0 |
0 |
|g 34
|t Pericyclic reactions 1: cycloadditions
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| 505 |
0 |
0 |
|g 35
|t Pericyclic reactions 2: sigmatropic and electrocyclic reactions
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| 505 |
0 |
0 |
|g 36
|t Participation, rearrangement, and fragmentation
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| 505 |
0 |
0 |
|g 37
|t Radical reactions
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| 505 |
0 |
0 |
|g 38
|t Synthesis and reactions of carbenes
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| 505 |
0 |
0 |
|g 39
|t Determining reaction mechanisms
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| 505 |
0 |
0 |
|g 40
|t Organometallic chemistry
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| 505 |
0 |
0 |
|g 41
|t Asymmetric synthesis
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| 505 |
0 |
0 |
|g 42
|t Organic chemistry of life
|
| 505 |
0 |
0 |
|g 43
|t Organic chemistry today
|
| 505 |
0 |
0 |
|t Figure acknowledgements
|
| 505 |
0 |
0 |
|t Periodic table of the elements
|
| 505 |
0 |
0 |
|t Index
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| 650 |
1 |
7 |
|2 spines
|a QUIMICA
|
| 650 |
1 |
7 |
|2 spines
|a ACIDOS INORGANICOS
|
| 650 |
1 |
7 |
|2 spines
|a PRODUCTOS QUIMICOS ORGANICOS
|
| 650 |
1 |
7 |
|2 spines
|a REACCIONES QUIMICAS
|
| 650 |
1 |
7 |
|2 spines
|a SALES INORGANICAS
|
| 700 |
1 |
|
|a Greeves, Nick
|
| 700 |
1 |
|
|a Warren, Stuart
|
| 931 |
|
|
|a DQO
|b QUIMICA ORGANICA I
|b QUIMICA ORGANICA II
|b CIENCIAS BIOLOGICAS
|
| 962 |
|
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|a info:eu-repo/semantics/book
|a info:ar-repo/semantics/libro
|b info:eu-repo/semantics/publishedVersion
|