|
|
|
|
| LEADER |
00000cam a22000007a 4500 |
| 001 |
EBOOKCENTRAL_ocn862369578 |
| 003 |
OCoLC |
| 005 |
20240329122006.0 |
| 006 |
m o d |
| 007 |
cr |n||||||||| |
| 008 |
131108s2013 xx o 000 0 eng d |
| 040 |
|
|
|a IDEBK
|b eng
|e pn
|c IDEBK
|d OCLCQ
|d DEBBG
|d OCLCQ
|d EBLCP
|d OCLCQ
|d OCLCL
|d OCLCQ
|
| 020 |
|
|
|a 1306090687
|q (ebk)
|
| 020 |
|
|
|a 9781306090681
|q (ebk)
|
| 029 |
1 |
|
|a DEBBG
|b BV041909068
|
| 035 |
|
|
|a (OCoLC)862369578
|
| 037 |
|
|
|a 540319
|b MIL
|
| 082 |
0 |
4 |
|a 547
|2 22
|
| 049 |
|
|
|a UAMI
|
| 100 |
1 |
|
|a Parsons, Andrew F.
|
| 245 |
1 |
0 |
|a Keynotes in Organic Chemistry.
|
| 260 |
|
|
|b Wiley,
|c 2013.
|
| 300 |
|
|
|a 1 online resource
|
| 336 |
|
|
|a text
|b txt
|2 rdacontent
|
| 337 |
|
|
|a computer
|b c
|2 rdamedia
|
| 338 |
|
|
|a online resource
|b cr
|2 rdacarrier
|
| 588 |
0 |
|
|a Print version record.
|
| 505 |
8 |
|
|a 2 Functional groups, nomenclature and drawing organic compounds -- 2.1 Functional groups -- 2.2 Alkyl and aryl groups -- 2.3 Alkyl substitution -- 2.4 Naming carbon chains -- 2.4.1 Special cases -- 2.5 Drawing organic structures -- Worked example -- Problems -- 3 Stereochemistry -- 3.1 Isomerism -- 3.2 Conformational isomers -- 3.2.1 Conformations of ethane (CH3CH3) -- 3.2.2 Conformations of butane (CH3CH2CH2CH3) -- 3.2.3 Conformations of cycloalkanes -- 3.2.4 Cyclohexane -- 3.3 Configurational isomers -- 3.3.1 Alkenes -- 3.3.2 Isomers with chiral centres -- Worked example -- Problems
|
| 505 |
8 |
|
|a 4 Reactivity and mechanism -- 4.1 Reactive intermediates: ions versus radicals -- 4.2 Nucleophiles and electrophiles -- 4.2.1 Relative strength -- 4.3 Carbocations, carbanions and carbon radicals -- 4.3.1 Order of stability -- 4.4 Steric effects -- 4.5 Oxidation levels -- 4.6 General types of reaction -- 4.6.1 Polar reactions (involving ionic intermediates) -- 4.6.2 Radical reactions -- 4.6.3 Pericyclic reactions -- 4.7 Ions versus radicals -- 4.8 Reaction selectivity -- 4.9 Reaction thermodynamics and kinetics -- 4.9.1 Thermodynamics -- 4.9.2 Kinetics
|
| 505 |
8 |
|
|a 4.9.3 Kinetic versus thermodynamic control -- 4.10 Orbital overlap and energy -- 4.11 Guidelines for drawing reaction mechanisms -- Worked example -- Problems -- 5 Halogenoalkanes -- 5.1 Structure -- 5.2 Preparation -- 5.2.1 Halogenation of alkanes -- 5.2.2 Halogenation of alcohols -- 5.2.3 Halogenation of alkenes -- 5.3 Reactions -- 5.3.1 Nucleophilic substitution -- 5.3.2 Elimination -- 5.3.3 Substitution versus elimination -- Worked example -- Problems -- 6 Alkenes and alkynes -- 6.1 Structure -- 6.2 Alkenes -- 6.2.1 Preparation -- 6.2.2 Reactions -- 6.3 Alkynes -- 6.3.1 Preparation
|
| 505 |
8 |
|
|a 6.3.2 Reactions -- Worked example -- Problems -- 7 Benzenes -- 7.1 Structure -- 7.2 Reactions -- 7.2.1 Halogenation -- 7.2.2 Nitration -- 7.2.3 Sulfonation -- 7.2.4 Alkylation: The Friedel-Crafts alkylation -- 7.2.5 Acylation: The Friedel-Crafts acylation -- 7.3 Reactivity of substituted benzenes -- 7.3.1 Reactivity of benzene rings: Activating and deactivating substituents -- 7.3.2 Orientation of reactions -- 7.4 Nucleophilic aromatic substitution (the SNAr mechanism) -- 7.5 The formation of benzyne -- 7.6 Transformation of side chains -- 7.7 Reduction of the benzene ring
|
| 590 |
|
|
|a ProQuest Ebook Central
|b Ebook Central Academic Complete
|
| 655 |
|
0 |
|a Electronic books.
|
| 758 |
|
|
|i has work:
|a Keynotes in organic chemistry (Text)
|1 https://id.oclc.org/worldcat/entity/E39PCGPwRMGFt4JpVXWwhP4xwC
|4 https://id.oclc.org/worldcat/ontology/hasWork
|
| 776 |
0 |
8 |
|i Print version:
|z 9781306090681
|
| 856 |
4 |
0 |
|u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=7103938
|z Texto completo
|
| 936 |
|
|
|a BATCHLOAD
|
| 938 |
|
|
|a ProQuest Ebook Central
|b EBLB
|n EBL7103938
|
| 938 |
|
|
|a ProQuest MyiLibrary Digital eBook Collection
|b IDEB
|n cis26589068
|
| 994 |
|
|
|a 92
|b IZTAP
|
