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|d OPELS
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|a 1394062565
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|a 9780323959476
|q electronic book
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|q electronic book
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|a (OCoLC)1394119155
|z (OCoLC)1394062565
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|a QD501
|b .V47 2023
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|a 541.39
|2 23/eng/20231004
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|a Verma, Dakeshwar Kumar.
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|a Handbook of Organic Name Reactions :
|b Reagents, Mechanism and Applications.
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| 264 |
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|a San Diego :
|b Elsevier,
|c 2023.
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| 300 |
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|a 1 online resource (481 p.)
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| 336 |
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
|2 rdamedia
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|a online resource
|b cr
|2 rdacarrier
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|a Front Cover -- Handbook of Organic Name Reactions -- Copyright Page -- Contents -- Foreword -- Preface -- 1 Organic reaction mechanism -- 1.1 Basics of organic chemistry -- 1.1.1 Inductive Effect -- 1.1.2 Electromeric Effect -- 1.1.3 Mesomeric effect/Resonating effect /Conjugation effect -- 1.1.4 Resonance -- 1.1.5 Hyperconjugation or no-bond resonance -- 1.2 Reaction intermediates: carbocation, carbanion, free radical, carbene, nitrene, and benzyne -- 1.2.1 Carbocation -- 1.2.2 Carbanion -- 1.2.3 Carbon-free radical -- 1.2.4 Carbene -- 1.2.5 Nitrene -- 1.2.6 Benzyne/aryne
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|a 1.3 Nucleophilic addition to carbon-heteroatoms multiple bonds -- 1.4 Electrophilic addition to carbon-carbon multiple bonds -- 1.4.1 Addition of bromine to alkenes -- 1.4.2 Regioselectivity of electrophilic addition to unsymmetrical alkenes -- 1.4.3 Formation of epoxide from alkene -- 1.4.4 Reaction of NBS to alkene -- 1.4.5 Iodo-and Bromo-lactonization -- 1.4.6 Addition of water molecule to alkene and alkynes -- 1.4.7 Dihydroxylation of alkenes -- 1.4.8 Ozonolysis -- 1.4.9 Hydroboration -- 1.5 Nucleophilic aliphatic substitution and neighboring group participation
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|a 1.6 Unimolecular nucleophilic substitution (SN1)reaction -- 1.7 Bimolecular nucleophilic substitution (SN2)reaction -- 1.8 Neighbouring group participation (NGP) -- 1.9 Substitution nucleophilic internal (SNi) Mechanism -- 1.10 Nucleophilic aromatic substitution -- 1.10.1 Addition-elimination mechanism (An activatedcomplex mechanism) -- 1.10.2 Elimination-addition mechanism (Benzyne mechanism) -- 1.11 Electrophilic aliphatic, alkenyl, and alkynyl substitution reaction -- 1.11.1 Unimolecular electrophilic aliphatic substitution (SE1) reaction
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|a 1.11.2 Bimolecular aliphatic electrophilic substitution reaction (SE1 and SEi) -- 1.11.3 Electrophilic substitution reaction at the allylic group -- 1.12 Electrophilic aromatic substitution reaction -- 1.13 Elimination reaction -- 1.13.1 Unimolecular elimination (E1) reaction -- 1.13.2 Bimolecular elimination E2 reaction -- 1.13.3 Unimolecular conjugated base (E1cB) Elimination reaction -- References -- 2 Reactions of aldehydes and ketones -- 2.1 Aldol condensation reaction -- 2.1.1 Cross-aldol condensation reaction -- 2.1.1.1 Reactivity of carbonyl compounds with nucleophilic agents
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|a 2.1.2 Henry nitroaldol condensation -- 2.1.3 Intramolecular aldol condensation -- 2.1.4 Barbas-list asymmetric aldol reaction -- 2.1.5 Mukaiyama aldol reaction -- 2.2 Baeyer-Villiger oxidation -- 2.3 Bamford-Stevens reaction -- 2.3.1 Selectivity in Bamford-Stevens reaction -- 2.4 Barton decarboxylation reaction -- 2.5 Barbier reaction -- 2.6 Barbier in situ Grignard reaction -- 2.7 Baer-Fischer amino sugar synthesis -- 2.8 Baylis-Hillman reaction -- 2.8.1 Intramolecular Baylis-Hillman reaction -- 2.9 Benzoin condensation -- 2.10 Bischler-Napieralski reaction
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| 500 |
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|a 2.11 Bouveault-Blanc reduction reaction
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| 650 |
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|a Chemical reactions.
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| 650 |
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|a Chemistry, Organic.
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| 700 |
1 |
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|a Dewangan, Yeestdev.
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| 700 |
1 |
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|a Verma, Chandrabhan.
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| 776 |
0 |
8 |
|i Print version:
|a Verma, Dakeshwar Kumar
|t Handbook of Organic Name Reactions
|d San Diego : Elsevier,c2023
|z 9780323959483
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| 856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/book/9780323959483
|z Texto completo
|
