[정답] 유기화학에서의 reaction response 매커니즘 (Writing Reaction Mechanisms In Organic Chemistry by Miller, Solomen) > primus7

[정답] 유기화학에서의 reaction response 매커니즘 (Writing Reaction Mechanisms In Or…

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5. The Ene Reaction 373
Determining the Number of Rings and/or [pi] Bonds
347
112
2. Formation of Carbocations 196
A. Nucleophilicity 37
A. Aromatic Carbocycles 26
B. Ei Elimination 122
Aldehydes and Ketones
Electrocyclic Reactions of Charged Species (Cyclopropyl

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3. Nucleophilic Addition to Carbonyl Compounds 123
B. Substrate 38
8. Carbenes 224
C.
B.

A. Ionization 196
A. Hydrolysis of Carboxylic Acid Derivatives 213
9. Nucleophiles and Electrophiles 37
Carbon (Carbonyl Groups)

A. Terminology 366
C. 1,4-Addition 218
E. Correlation Diagrams 388
8. Rearrangement of Radicals 303
312
Appendix B Symbols and Abbreviations Used in Chemical Notation 455
A. Homolytic Bond Cleavage 284
11.
B. The Pinacol Rearrangement 206

1. Introduction 283
A. E2 Elimination 120
F. Frontier Orbitals 392
6. AMolecular Orbital View of Pericyclic Processes 379
Determining the Thermodynamic Feasibility of Radical
4. Electron-Rich Species: Bases or Nucleophiles? 76
A. Singlet and Triplet Carbenes 225
1. Balancing Equations 64
[정답] 유기화학에서의 reaction response 매커니즘 (Writing Reaction Mechanisms In Organic Chemistry by Miller, Solomen)
6. Addition of Radicals 294
A. The S[subscript N]2 Reaction 106
9. Solvent Effects 86
2 General Principles for Writing Reaction Mechanisms
B. Theories of Pericyclic Reactions 344
C. Reactions of Carbenes 227
2
2. Using Arrows to Show Moving Electrons 66
C.
Relative Acidities of Common Organic and Inorganic

9. The S[subscript RN] 1 Reaction 307
C. Organic Radicals Derived from Functional Groups 286
A. Electron-Deficient Nitrogen 232
2

B. Selection Rules for Sigmatropic Rearrangements 368
Reactions of Carbon Nucleophiles with Carbonyl
B. Rearrangements Involving Electrophilic Nitrogen 233
3. Cycloadditions 355
8. Acidity and Basicity 32
3. Radical Chain Processes 287
A. Drawing Resonance Structures 18

3 Reactions of Nucleophiles and Bases
A. Selection Rules for Electrocyclic Reactions 346
Reaction of Nitrogen-Containing Nucleophiles with
B. Hydrolysis and Formation of Acetals and Orthoesters 216
Compounds

296
Reactions
Index
5 Radicals and Radical Anions

7. Driving Forces for Reactions 82
A. Addition of Organometallic Reagents 123
85
1 Introduction: Molecular Structure and Reactivity
D. Cycloadditions of Charged Species 362
353
and Disrotatory Processes)
2. Formation of Radicals 284
4 Reactions Involving Acids and Other Electrophiles
7 Additional Problems 417
2. Eliminations at Saturated Carbon 120
Substances
4. Radical Inhibitors 290
How to Write Lewis Structures and Calculate Formal
B. Molecular Orbitals 380
설명
C. Drawing the Lewis Structure 3
B. Aromatic Heterocycles 27
A. Intermolecular Radical Addition 294
1. Introduction 343
D. HOMOs and LUMOs 387

1. Nucleophilic Substitution 106
Preface to First Edition xiii
4. Rearrangement of Carbocations 200
Appendix A Lewis Structures of Common Functional Groups 453
6. Aromaticity and Antiaromaticity 26
(Degree of Unsaturation
A. Determining the Number of Bonds 2
B. The Benzilic Acid Rearrangement 142
Charges
D. Formal Charge 6
B. Rules for Resonance Structures 23

D. Loss of CO 300
C. Secondary Interactions 361
C. Antiaromaticity 28
4. Sigmatropic Rearrangements 366
3. The Fate of Carbocations 199
128
Intramolecular Radical Addition: Radical Cyclization

A. Types of Pericyclic Reactions 343
B. Loss of a Ketone 300

B.
Nucleophilic Substitution at Aliphatic sp[superscript 2]

6 Pericyclic Reactions
Stereochemistry of Electrocyclic Reactions (Conrotatory

A RadicalMechanism for the Rearrangement of Some
C. Solvent 39
1.
Preface to the Second Edition xi
Products
Appendix C
C. Nucleophilic Substitution at Aromatic Carbons 116
8.
5. AdditionalMechanisms in Basic Media 144
A. The Favorskii Rearrangement 141
B.
10. A LastWord 88
7. Tautomers and Equilibrium 29
Reactions
B. Formation of a Small Stable Molecule 84
A. Leaving Groups 83
5. Electrophilic Addition 208
C. Loss of N[subscript 2] 300
화공, 화학, 솔루션, organic, 유기
B.
B.
7. Electrophilic Aromatic Substitution 220
3. Geometry and Hybridization 14
5. Trimolecular Steps 78
3. Mechanisms in Acidic and Basic Media 69

A. Regiospecificity 208
6. Acid-Catalyzed Reactions of Carbonyl Compounds 213
A. Terminology of Cycloadditions 355
5. Resonance Structures 18
4. Base-Promoted Rearrangements 141
C. Generating and Analyzing [pi] Molecular Orbitals 382
5.
1. Stability of Carbocations 195
Structural Relationships between Starting Materials and
B. Selection Rules for Cycloadditions 358
10. The Birch Reduction 310
Table of Contents
Cations)
B. Addition of an Electrophile to a [pi] Bond 197
Anions
457
B. Hydrogen Abstraction from Organic Molecules 285
4. Electronegativities and Dipoles 16
C. Rearrangement Involving Electron-Deficient Oxygen 238
A. The Dienone-Phenol Rearrangement 204

A. Loss of CO[subscript 2] 299
2. Electrocyclic Reactions 346

6. Stability of Intermediates 79
B. Stereochemistry 209
292
130
9. Electrophilic Heteroatoms 231
C. Reaction of an Alkyl Halide with a Lewis Acid 199
B. Formation of Carbenes 226
A. Orbitals 379
2. Representations of Organic Compounds 12
순서

7. Fragmentation Reactions 299
레포트 > 공학,기술계열
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