愚愚学园 化学工程与技术 [Free ebook] Handbook of Spectroscopic Data: Chemistry - UV,IR,PMR,CNMR and Mass Spectroscopy

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[Free ebook] Handbook of Spectroscopic Data: Chemistry - UV,IR,PMR,CNMR and Mass Spectroscopy

Handbook of Spectroscopic Data: Chemistry - UV,IR,PMR,CNMR and Mass Spectroscopy
by: B. Mistry
•Publisher:   Oxford Book Company
•Number Of Pages:   250
•Publication Date:   2009-08-01
•IN-10 / ASIN:   8189473867
•IN-13 / EAN:   9788189473860

"For any organic chemists intending to gain information about a substance, techniques such as ultraviolet, infrared, nuclear magnetic resonance and mass spectra copy are important ones. This book envisages in it much useful spectral data in table and charts. For graduate and post-graduate students and organic research chemist who are not spectro scopists, the book can be a valuable reference for the interpretation of most spectra. In most cases, the organic chemist should be able to interpret a spectrum using these compilations of data without having to search through more detailed texts in the areas." (jacket)

Contents
1. Ultraviolet Spectroscopy 1
2. Infrared Spectroscopy 26
3. Proton Magnetic Resonance Spectroscopy 64
4. Be NMR Spectroscopy 99
5. Mass Spectrometry 128
6. Structural Data Obtainable from Different Spectra 237
Index 240

Index
Abietic acid, 7
Absorption frequencies of:
alkenes, 45-46
aromatic homocyclic
compounds, 47-49
common organic compounds,
27-34
Alcohols: 13C chemical shifts,
111-12
Alkenes and alkynes: 13C
chemical shifts, 104-08
Amines: 13C chemical shifts, 114
Aromatic compounds:
13C chemical shifts, 108-11
Aromatic molecules:
carbonyl compounds, 13-20
dienes, 7-8
enones, 10-13
polyenes, 8-9
Aromatic systems and
derivatives: absorption
characteristics, 16-18
Auxochrome substituents, 6
Benzene chromophore, 5-6
Branched chain alkanes, 134
Calculating absorption maxima
of:
aromatic molecules, 5-13
carbonyl compounds, 3-5
unsaturated compounds, 1-3
Carbonyl compounds, 3-4
Carboxylic acids, ester,
chlorides, anhydreds, amides
and nitriles: 13C chemical
shits, 116-20
Chemical shifts, multiplicities and
coupling constants, 86-88
Chemical shifts:
alicyclic rings, 72
alkyne protons, 77
fused aromatic rings, 78
heteroaromatic rings, 79
heterocyclic rings, 72-73
methyl, methylene and
methane protons, 65-67
Index
miscellanceous alkenes,
75-77
monosubstituted benzene
rings proton, 77-78
substituent effects, 70-71
two/three functional groups,
68-70
unsaturated and aromatic
systems, 73-75
Chromophore substituents, 6
Common fragmentation ions,
225-32
Common fragmentation lost,
233-35
Coupling constants, 122
Cross conjugation, 1
Cutoff wavelength, 19-20
Cyclic diene, 1
Dicarbonyl compounds, 12
Diene absorption: Woodword's
and Fieser's rules, 2
Diens and triens: kinds of, 1-2
Different spectra: structural data
obtainable, 237-39
Effects of chemical shifts on:
alicyclic and heterocyclic
rings, 73-80
protons on heteroatoms,
80-81
single functional groups,
65-67
two/three functional groups,
68-71
Enone and dienone absorption
rules, 4-5
Enone: solvent correlations, 5
Ergosterol, 8
241
Ethers, acetols and epoxides:
13C chemical shifts, 112-13
Exact masses of isotopes,
129-30
Fragmentation process:
alcohols, 137-40
aldehydes, 144-45
alkanes, 132-34
alkenes, 135-36
amides, 151-52
amines, 149-51
aromatic hydrocarbons,
136-37
carboxylic acids and esters,
147-49
ethens, 142-43
ketones, 145-47
phenols and other aromatic
alcohols, 140-42
Halides: 13C chemical shifts,
113-14
Heteroannular diene, 2
Heteroatoms, 80-81
Homoannular diene, 2
Incremental shits of aromatic
carbon atoms of
monosaturat.::d benzenes,
108-10
Incremental substituents effects,
102
Infrared absorption and structure
of organic compounds:
correlations, 34-35
Ketones and aldehydes: 13C
chemical shifts, 115-16
242
Linear and branched alkanes:
13C chemical shifts, 94-104
Linear conjugation, 1
Mass spectroscopy, 128-235
Mass spectrum, 128
McLafferty rearrangements, 135,
136,144,147
Molecular ion, 128-29
Mulling oils, 58
Multiplicities, 13C chemical shifts
and couplings of common
NMR solvents, 123-24
NMR spectroscopy, 90-127
NMR table of correlations of
chemical shifts of protons,
88-93
Ortho and meta substitution,
15
Oximes: 13C chemical shifts,
120
Para substitution, 14
Parameters of 13C chemical
shifts, 100
Polycyclic aromatic compounds:
absorption characteristics, 15
Polyenes,3
Proton magnetic resonance
spectroscopy, 64-93
Proton spin coupling constants,
81-85
Protons on heteroatoms,
80-81
Index
Recognition of molecular ion
peak, 131-32
Relative isotopic abundance of
common elements, 130
Retro-Diels-Alder reaction, 135
Scott's rule for "-max of ET band,
6-7
Semicyclic diene, 1-2
Shielding constants, 68-69
Solvents and mulling oils: infrared
tranission characteristics,
57-58
Some CJCH) values, 120-21
Some eJCH) values, 121-22
Spin coupling, 120-22
Stretching frequencies of:
carbonyl compounds, 49-53
cyclic and acyclic systems, 47
Substituent constants, 74-75
Substituent effects on chemical
shifts, 70-71
Table of 13C correlation for
chemical classes, 124-27
Thiols, sulfides and disulfides:
13Cchemicalshifts, 114-15
Trans f3-carotene, 8-9
Translycopene, 9
Ultraviolet spectroscopy, 1-20
Variations of carbonyl stretching
band,53-54
Vibration modes of amines and
amino acids, 55-56