GLOSSARY OF TERMS USED IN PHYSICAL ORGANIC CHEMISTRY
(IUPAC Recommendations 1994)

References

(Reports and Rules drafted by other IUPAC Commissions are indicated by an asterisk.)

ABRAHAM, M. H., GRELLIER, P. L., and MCGILL, R. A. (1988), J. Chem. Soc., Perkin Trans. II, 339-345. solvophobicity parameter

ADAMS, D. L. (1992), J. Chem. Educ., 69, 451-452. regioselectivity

AHRLAND, S. (1979), Pure Appl. Chem., 51, 2019-2039. hydration

ALBERY, W. J. (1967), Prog. Reaction Kinetics, 4, 353-398. potential energy (reaction) surface

ALBERY, W. J. (1980), Annu. Rev. Phys. Chem., 31, 227-263. Marcus equation

ARGILE, A., CAREY, A. R. E., FUKATA, G., HARCOURT, M., MORE O'FERRALL, R. A., and MURPHY, M. G. (1985), Isr. J. Chem., 26, 303-312. reactivity-selectivity principle

ATKINS, P. W. (1974), "Quanta: a Handbook of Concepts", Clarendon Press, Oxford. aromatic, electronegativity, resonance

BALDWIN, J. E. (1976), J. Chem. Soc., Chem. Commun., 734-736. Baldwin's rules

BARTLETT, P. D. (Ed.) (1965), "Nonclassical Ions", Benjamin, New York. nonclassical carbocation

BARTMESS, J. R., and MC IVER, R. T. (1979), "Gas-Phase Ion Chemistry", Vol. 2, (BOWERS, M.-T., Ed.), Academic Press, New York, Chap. 11. gas phase acidity

BENSON, S. W. (1976), "Thermochemical Kinetics", Second Edition, Wiley-Interscience, New York. additivity principle

BENTLEY, T. W., and LLEWELLYN, G. (1990), Progr. Phys. Org. Chem., 17, 121-158. Grunwald-Winstein equation

BENTLEY, T. W., and SCHLEYER, P. v. R. (1977), Adv. Phys. Org. Chem., 14, 1-67. Grunwald-Winstein equation

BERNASCONI, C. F. (1976), "Relaxation Kinetics", Academic Press, New York. chemical relaxation

BERNASCONI, C. F. (1992), Adv. Phys. Org. Chem., 27, 119-238. imbalance, synchronization

BERSON, J. A. (1972), Acc. Chem. Res., 5, 406-414. subjacent orbital

BINSCH, G., ELIEL, E. L., and KESSLER, H. (1971), Angew. Chem., Int. Ed. Engl., 10, 570-572. degenerate rearrangement

BIOCHEMICAL NOMENCLATURE (1992). JCBN/NC-IUBMB Newsletter, in "Biochemical Nomenclature and Related Documents", 2nd edn., Portland Press, London, 335. ligand

BORDWELL, F. G., and LYNCH, T.-Y. (1989), J. Am. Chem. Soc., 111, 7558-7562. captodative effect

BREDT, J. (1924), Justus Liebigs Ann. Chem., 437, 1-13. Bredt's rule

BROOKHART, M., and GREEN, M. L. H. (1983), J. Organomet. Chem., 250, 395-408. agostic

BUNCEL, E., CRAMPTON, M. R., STRAUSS, M. J., and TERRIER, F. (1984), "Electron Deficient Aromatic- and Heteroaromatic- Base Interactions. The Chemistry of Anionic Sigma Complexes". Elsevier, Amsterdam. Meisenheimer adduct

BUNCEL, E., and RAJAGOPAL, S. (1990), Acc. Chem. Res., 23, 226-231. solvatochromism

BUNCEL, E., and WILSON, H. (1987), J. Chem. Educ., 64, 475-480. reactivity-selectivity principle

BUNNETT, J. F., and OLSEN, F. P. (1966), Can. J. Chem., 44, 1899-1916, 1917-1931. Bunnett-Olsen equation

BURKERT, U., and ALLINGER, N. L. (1982), "Molecular Mechanics", ACS Monograph 177, American Chemical Society, Washington, D.C. molecular mechanics calculations

CANNON, R. D. (1980), "Electron Transfer Reactions", Butterworths, London. intrinsic barrier

CAREY, F. A., and SUNDBERG, R. J. (1990), "Advanced Organic Chemistry, Part A", Plenum, New York, p. 133-138. A-value

CHAPMAN, N. B., and SHORTER, J. (Eds.) (1972), "Advances in Linear Free Energy Relationships", Plenum, New York. correlation analysis, extended Hammett equation, [sigma]-constant

CHAPMAN, N. B., and SHORTER, J. (Eds.) (1978), "Correlation Analysis in Chemistry: Recent Advances", Plenum, New York. extended Hammett equation, Ritchie equation, [sigma]-constant

CHARTON, M. (1984), J. Org. Chem., 49, 1997-2001. Swain-Lupton equation

CHARTON, M. (1987), Progr. Phys. Org. Chem., 16, 287-315. electromeric effect, extended Hammett equation, steric effect

CHARTON, M. (1989), "The Chemistry of Double-Bonded Functional Groups". Supplement A, Volume 2 (PATAI, S., Ed.), Wiley, Chichester, Chap. 5. quantitative structure-activity realtionships (QSAR)

CHASTRETTE, M., RAJZMANN, M., CHANON, M., and PURCELL, K. F. (1985), J. Am. Chem. Soc., 107, 1-11. Hildebrand parameter

CODATA (1974), Codata Bulletin No. 13, Dec. 1974, p. 4. rate of reaction

CONNOR, K. A. (1991), "Chemical Kinetics", VCH, New York, p. 368. compensation effect

COX, R. A., and YATES, K. (1978), J. Am. Chem. Soc., 100, 3861-3867. Cox-Yates equation

COX, R. A., and YATES, K. (1981), Can. J. Chem., 59, 2116-2124. Cox-Yates equation

COX, R. A., and YATES, K. (1983), Can. J. Chem., 61, 2225-2243. acidity function

CRAM, D. J., HO, S. P., KNOBLER, C. B., MAVERICK, E., and TRUEBLOOD, K. N. (1986), J. Am. Chem. Soc., 108, 2989-2998. crown

DANHEISER, R. L., GERE, S. K., and SARD, H. (1982), J. Am. Chem. Soc., 104, 7670-7672. annulation

DEWAR, M. J. S. (1969), "The Molecular Orbital Theory for Organic Chemistry", McGraw-Hill, New York. Bell-Evans-Polanyi principle

DEWAR, M. J. S. (1971), Angew. Chem., Int. Ed. Engl., 10, 761-776. aromatic, chelotropic reaction

DIETRICH, B., LEHN, J. M., and SAUVAGE, J. P. (1969), Tetrahedron Lett., 2889-2892. cryptand

DIMROTH, K., REICHARDT, C., SIEPMANN, T., and BOHLMANN, F. (1963), Justus Liebigs Ann. Chem., 661, 1-37. Dimroth-Reichardt ET-parameter

EBERSON, L. (1987), "Electron Transfer Reactions in Organic Chemistry", Springer, Berlin. electron transfer catalysis, outer sphere (electron transfer)

EHRENSON, S., BROWNLEE, R. T. C., and TAFT, R. W. (1973), Progr. Phys. Org. Chem., 10, 1-80. dual substituent parameter equation, electromeric effect, inductive effect

ELIEL, E. L. (1962), "Stereochemistry of Carbon Compounds", McGraw Hill, New York. Curtin-Hammett principle, stereoselective, stereospecific

EXNER, O. (1973), Progr. Phys. Org. Chem., 10, 411-482. isokinetic relationship

EXNER, O. (1988), "Correlation Analysis of Chemical Data", Plenum, New York, SNTL, Prague. reactivity-selectivity principle

FAINBERG A. H., and WINSTEIN, S. (1956), J. Am. Chem. Soc., 78, 2770-2777. Grunwald-Winstein equation

FALBE, J., REGITZ, M. (Eds) (1990), Römpp Chemie Lexikon, 9th edition, Vol. 3. Thieme, Stuttgart. halochromism

FARCASIU, D. (1975), J. Chem. Educ., 52, 76-79. Hammond principle

FAWCETT, F. S. (1950), Chem. Rev., 47, 219-274. Bredt's rule

FLEMING, I. (1976), "Frontier Orbitals and Organic Chemical Reactions", Wiley, New York. frontier orbital

FUKUI, K., YONEZAWA, T., and SHINGU, H. (1952), J. Chem. Phys., 20, 722-725. frontier orbital

GARRATT, P. J. (1986), "Aromaticity", Wiley, New York. aromatic

GIESE, B. (1984), Acc. Chem. Res., 17, 438-442. isoselective relationship

GILLESPIE, R. J. (1968), Acc. Chem. Res., 1, 202-209. superacid

GOLD, V. (1969), Adv. Phys. Org. Chem., 7, 259-331. fractionation factor, isotopic

GOLD, V. (1979), Nouveau J. Chim., 3, 69-71. chemical flux

GOMPPER, R. (1964), Angew. Chem., Int. Ed. Engl., 3, 560-570. ambident

GRILLER, D., and INGOLD, K. U. (1976), Acc. Chem. Res., 9, 13-19. persistent

GROB, C. A. (1969), Angew. Chem., Int. Ed. Engl., 8, 535-546. fragmentation

GRUNWALD, E., and WINSTEIN, S. (1948), J. Am. Chem. Soc., 70, 846-854. Grunwald-Winstein equation

GULDBERG, C. M., and WAAGE, P. (1879), J. prakt. Chem., 19, 69-114. mass-law effect

GUTMANN, V. (1976), Coord. Chem. Rev., 18, 225-255. acceptor number (AN), donor number (DN)

HALEVI, E. A. (1992), "Orbital Symmetry and Reaction Mechanisms. The Ocams View", Springer, Berlin. orbital symmetry

HAMMETT, L. P. (1940, 1970), "Physical Organic Chemistry", 1st and 2nd editions, McGraw Hill, New York. acidity function, Bunnett-Olsen equation, Hammett equation, Zucker-Hammett hypothesis

HAMMOND, G. S. (1955), J. Am. Chem. Soc., 77, 334-338. Hammond principle

HANSCH, C., and LEO, A. J. (1979), "Substituent Constants for Correlation Analysis in Chemistry and Biology", Wiley, New York. Hansch constant

HANSCH, C., LEO, A., and TAFT, R. W. (1991), Chem. Rev., 91, 165-195. Swain-Lupton equation

HANZLIK, R. P., HOGBERG, K., and JUDSON, C. M. (1984), Biochemistry, 23, 3048-3055. NIH-shift

HARTMANNS, J., KLENKE, K., and METZGER, J. O. (1986), Chem. Ber., 119, 488-499. comproportionation

HASSNER, A. (1968), J. Org. Chem., 33, 2684-2686. regioselectivity

HEHRE, W. J., DITCHFIELD, R., RADOM, L., and POPLE, J. A. (1970), J. Am. Chem. Soc., 92, 4796-4801. isodesmic reaction

HEILBRONNER, E. (1964), Tetrahedron Lett., 1923-1928. Möbius aromaticity

HENDRICKSON, J. B., CRAM, D. J., and HAMMOND, G. S. (1970), "Organic Chemistry", 3rd edition, McGraw Hill, New York. Chapter 18. oxidation

HINE, J. (1977), Adv. Phys. Org. Chem., 15, 1-61. least nuclear motion, principle of

HIRSCH, J. A. (1967), Top. in Stereochem., 1, 199-222. A-value

HO, T.-L. (1977), "Hard and Soft Acids and Bases Principle in Organic Chemistry", Academic Press, New York. hard acid, symbiosis

HOEFNAGEL, A. J., OOSTERBEEK, W., and WEPSTER, B. M. (1984), J. Org. Chem. , 49, 1993-1997. Swain-Lupton equation

HOFFMANN, R. (1982), Angew. Chem., Int. Ed. Engl., 21, 711-724. radical

HOFMANN, A. W. (1851), Justus Liebigs Ann. Chem., 78, 253-286; 79, 11-39. Hofmann rule

HOZ, S. and BUNCEL, E. (1985), Isr. J. Chem., 26, 313-319. [alpha]-effect

HUISGEN, R. (1968), Angew. Chem., Int. Ed. Engl., 7, 321-328. cycloaddition

HUISGEN, R., GRASHEY, R., and SAUER, J. (1964), "The Chemistry of Alkenes", (PATAI, S., Ed.), Wiley Interscience, London, p. 739. cycloaddition

INGOLD, C. K. (1953), "Structure and Mechanism in Organic Chemistry", Cornell University Press, New York. electromeric effect, inductomeric effect, partial rate factor, polarizability, tautomerism

ISAACS, N. S. (1987), "Physical Organic Chemistry", Longman, Essex. Curtin-Hammett principle

*IUPAC ANALYTICAL CHEMISTRY (1982). IUPAC: Analytical Chemistry Division, Pure Appl. Chem., 54, 1533-1554. excited state, ground state

*IUPAC ATMOSPHERIC GLOSSARY (1990). IUPAC: Applied Chemistry Division: Commission on Atmospheric Chemistry. Glossary of Atmospheric Chemistry Terms, Pure Appl. Chem., 62, 2167-2219. matrix isolation

*IUPAC CHEMICAL KINETICS (1981). IUPAC: Physical Chemistry Division: Commission on Chemical Kinetics. Pure Appl. Chem., 53, 753-771.

*IUPAC CHEMICAL KINETICS (1991). IUPAC: Physical Chemistry Division: Commission on Chemical Kinetics. A Glossary of Terms Used in Chemical Kinetics Including Reaction Dynamics. Fifth Draft, provisional. elementary reaction

*IUPAC CLASS NAMES (1993). IUPAC: Organic Chemistry Division. Glossary of Class Names of Organic Compounds and Reactive Intermediates Based on Structure. IDCNS and public review. annulene, aryne, benzyne, nitrenium ion, onium ion; now published in Pure Appl. Chem., 67, 1307-1375 (1995).

*IUPAC COMPENDIUM (1987). IUPAC: Compendium of Chemical Terminology, (GOLD, V., LOENING, K. L., MCNAUGHT, A. D., and SEHMI, P., Eds.), Blackwell, Oxford. scavenger

*IUPAC INORGANIC NOMENCLATURE (1990). IUPAC: Nomenclature of Inorganic Chemistry, Recommendations 1990, (LEIGH, G. J., Ed.), Blackwell, Oxford. complex, coordination number, hapto, oxidation, oxidation number

*IUPAC INORGANIC RULES (1970). IUPAC: Nomenclature of Inorganic Chemistry. Definitive Rules 1970: Butterworths, London. complex, oxidation, oxidation number

*IUPAC MANUAL (1979). IUPAC: Manual of symbols and terminology for physico-chemical quantities and units. Pure Appl. Chem., 51, 1-41. Gibbs energy, ligand, rate of reaction

*IUPAC MANUAL APPENDIX II (1972). IUPAC: Manual of symbols and terminology for physico-chemical quantities and units. Appendix II. Pure Appl. Chem., 31, 577-638. critical micelle concentration, micelle

*IUPAC MANUAL APPENDIX V (1981). IUPAC: Sub-Committee on Chemical Kinetics. Manual of symbols and terminology for physico-chemical quantities and units. Appendix V. Symbolism and terminology in chemical kinetics. Pure Appl. Chem., 53, 753-771. rate of reaction

*IUPAC MASS SPECTROSCOPY (1991). IUPAC: Physical Chemistry Division: Commission on Molecular Structure and Spectroscopy; Subcommittee on Mass Spectroscopy. Pure Appl. Chem., 63, 1541. fast-atom bombardment (FAB) mass spectroscopy

IUPAC NAMES FOR HYDROGEN ATOMS (1988). IUPAC: Organic Chemistry Division: Commission on Physical Organic Chemistry. Names for Hydrogen Atoms, Ions, and Groups, and for Reactions Involving Them. Pure Appl. Chem., 60, 1115-1116. hydron

*IUPAC NOMENCLATURE GUIDE (1993). IUPAC: Organic Chemistry Division: Commission on Organic Nomenclature. Guide to IUPAC Nomenclature of Organic Compounds, Blackwell, Oxford, 1993. carbocation, carbonium ion, radical

*IUPAC ORGANIC RULES (1979). IUPAC: Nomenclature of organic chemistry: definitive rules, 1979. Sections A, B, C, D, E, F, and H. Pergamon Press, Oxford. anti

*IUPAC PHOTOCHEMICAL GLOSSARY (1988). IUPAC: Organic Chemistry Division: Commission on Photochemistry. Glossary of Terms Used in Photochemistry. Pure Appl. Chem., 60, 1055-1106.

*IUPAC PHOTOCHEMICAL GLOSSARY (1992). IUPAC: Organic Chemistry Division: Commission on Photochemistry. Glossary of Terms Used in Photochemistry. Draft 1, provisional. biradical, bathochromic shift, charge transfer complex; configuration (electronic), excimer, exciplex, hypsochromic shift, inner sphere (electron transfer), quantum yield, relaxation

IUPAC PHYSICAL ORGANIC GLOSSARY (1979). IUPAC: Organic Chemistry Division: Commission on Physical Organic Chemistry. Glossary of Terms Used in Physical Organic Chemistry. Provisional. Pure Appl. Chem., 51, 1725-1801.

IUPAC PHYSICAL ORGANIC GLOSSARY (1983). IUPAC: Organic Chemistry Division: Commission on Physical Organic Chemistry. Glossary of Terms Used in Physical Organic Chemistry. Pure Appl. Chem., 55, 1281-1371. linear free-energy relation

*IUPAC POLYMERS (1981). IUPAC: Commission on Macromolecular Nomenclature. Stereochemical definitions and notations relating to polymers. Pure Appl. Chem., 53, 733-752. stereospecificity

*IUPAC QUANTITIES (1988). IUPAC: Physical Chemistry Division: Commission on Physicochemical Symbols, Terminology and Units."Quantities, Units and Symbols in Physical Chemistry", MILLS, I. CVITAS, T., HOMANN, K., KALLAY, N., and KUCHITSU, K., Eds.), Blackwell, Oxford.

IUPAC REACTION MECHANISMS (1989). IUPAC: Organic Chemistry Division: Commission on Physical Organic Chemistry. System for Symbolic Representation of Reaction Mechanisms. Pure Appl. Chem., 61, 23-56. left-to-righ convention, primitive change

*IUPAC STEREOCHEMICAL TERMINOLOGY (1993). IUPAC: Organic Chemistry Division: Basic Terminology of Stereochemistry. IDCNS and public review. anti, asymmetric induction, configuration, conformation, diastereoisomerism, epimer, isotopomer, optical yield, stereoselectivity; now published as Basic Terminology of Stereochemistry (IUPAC Recommendations 1996) in Pure Appl. Chem., 68, 2193-2222 (1996).

IUPAC TERMINOLOGY FOR TRANSFORMATIONS (1989). IUPAC: Organic Chemistry Division: Commission on Physical Organic Chemistry. Terminology for Organic Chemical Transformations. Pure Appl. Chem., 61, 725-768. transformation

JACKSON, C. J., GAZZOLO, F. H. (1900),Am. Chem.Soc., 23, 376-396. Meisenheimer adduct

JEFFORD, C. W., BERNARDINELLI, G., WANG, Y., SPELLMEYER, D. C., BUDA, A., and HOUK, K. N. (1992), J. Am. Chem. Soc., 114, 1157-1165. torquoselectivity

JENCKS, W. P. (1972), Chem. Rev., 72, 705-718. More O'Ferrall-Jencks diagram, potential energy (reaction) surface

JENCKS, W. P. (1980), Acc. Chem. Res., 13, 161-169. More O'Ferrall-Jencks diagram

JENCKS, W. P. (1985), Chem. Rev., 85, 511-527. Bell-Evans-Polayi principle, potential energy (reaction) surface

JOHNSON, C. D. (1973), "The Hammett Equation", Cambridge University Press. [sigma]-constant

JOHNSON, C. D. (1975), Chem. Rev., 75, 755-765. reactivity-selectivity principle

JORGENSEN, W. L., and SALEM, L. (1973), "The Organic Chemist's Book of Orbitals", Academic Press, New York. sigma, pi

JUNG, M.E. (1976), Tetrahedron, 32, 3-31. annulation

KAMLET, M. J., ABBOUD, J. L. M., and TAFT, R. W. (1981), Progr. Phys. Org. Chem., 13, 485-630. Kamlet-Taft solvent parameters

KEESE, R., and KREBS, E.-P. (1972), Angew. Chem., Int. Ed. Engl., 11, 518-520. Bredt's rule

KIRKWOOD, J. G., and WESTHEIMER, F. H. (1938), J. Chem. Phys., 6, 506-512, 513-517. field effect

KLYNE, W., and PRELOG, V. (1960), Experientia, 16, 521-523. anti

KOHNSTAM, G. (1967), Adv. Phys. Org. Chem., 5, 121-172. heat capacity of activation

KOPPEL, I. A., and PALM, V. A. (1972), "Advances in Linear Free Energy Relationships". (CHAPMAN, N. B., and SHORTER, J., Eds), Plenum Press, New York, Chap. 5. Koppel-Palm solvent parameters

KOSOWER, E. M. (1958), J. Am. Chem. Soc., 80, 3253-3260. Z-value

KOSOWER, E. M. (1968), "An Introduction to Physical Organic Chemistry". Wiley, New York. cybotactic region

LEHN, J.-M. (1993), Science, 260, 1762-1763. supramolecule

LEFFLER, J. E. (1953), Science, 117, 340-341. Hammond principle

LEFFLER, J. E. (1955), J. Org. Chem., 20, 1202-1231. isokinetic realtionship

LEFFLER, J. E., and GRUNWALD, E. (1963), "Rates and Equilibria of Organic Reactions", Wiley, New York, pp. 77-86. chemical relaxation, Hammond principle

LIAS, S. G., LIEBMAN, J. F., and LEVIN, R. P. (1984), J. Phys. Chem. Ref. Data, 13, 695-808. proton affinity

LITTLER, J. S. (1970), "Essays on Free-Radical Chemistry". Special Publication No. 24, p. 383. Chemical Society, London. outer sphere (electron transfer)

LONG, F. A., and PAUL, M. A. (1957), Chem. Rev., 57, 935-1010. Zucker-Hammett hypothesis

LUCCHINI, V., MODENA, G., SCORRANO, G., COX, R. A., and YATES, K. (1982), J. Am. Chem. Soc., 104, 1958-1959. Cox-Yates equation

LUO, X.-L., and CRABTREE, R. H. (1989), J. Am. Chem. Soc., 111, 2527-2535. agostic

LWOWSKI, W. (1970), "Nitrenes", Interscience, New York. nitrene

MARCUS, R. A. (1964), Annu. Rev. Phys. Chem., 15, 155-196. Marcus equation

MARCUS, R. A. (1966), J. Chem. Phys., 45, 4493-4499, 4500-4504. reaction coordinate

MARKOWNIKOFF, W. (1870), Justus Liebigs Ann. Chem., 153, 228-259 (p 256). Markownikoff rule

MASLAK, P., and NARVAEZ, J. N. (1990), Angew. Chem., Int. Ed. Engl., 29, 283-285. mesolytic cleavage

MAYO, P. DE (1980), "Rearrangements in Ground and Excited States", Vols. I-III, Academic Press, New York. molecular rearrangement

MORE O'FERRALL, R. A. (1970), J. Chem. Soc. (B), 274-277. More O'Ferrall-Jencks diagram, potential energy (reaction) surface

MULLIKEN, R. S. (1955), J. Chem. Phys., 23, 1833-1840, 1841-1846, 2338-2342, 2343-2346. charge population

OLAH, G. A. (1985), "Superacids". Wiley, New York. superacid

OLAH, G. A. (Ed.) (1990), "Cage Hydrocarbons". Wiley, New York. cage compound

OLAH, G. A., and OLAH, J. A. (1970), "Carbonium Ions" Vol. II, (OLAH, G. A., and SCHLEYER, P. v. R., Eds.), Wiley, New York, p. 715. superacid

OLAH, G. A., and SCHLEYER, P. v. R. (1972), "Carbonium Ions", Vols I-V, Wiley, New York. carbocation, carbonium ion

OLAH, G. A., SURYA PRAKASH, G. K., WILLIAMS, R. E., FIELD, L. D., and WADE, K. (1987), "Hypervalent Chemistry", Wiley, New York. bridged carbocation

PAULING, L. (1967), "The Chemical Bond", Cornell University Press, Ithaca, New York. bond

PEARSON, R. G. (1963), J. Am. Chem. Soc., 85, 3533-3539. hard acid

PEARSON, R. G. (1973), "Introduction to Hard and Soft Acids and Bases". Dowden, Hutchinson, Ross, Stroudsburg. hard acid

PEDERSEN, C. J. (1967), J. Am. Chem. Soc., 89, 7017-7036. crown

RADOM, L. (1982), Progr. Theor. Org. Chem., 3, 1. hyperconjugation

REETZ, M. (1972), Angew. Chem., Int. Ed. Engl., 11, 129-130, 130-131. dyotropic rearrangement

REICHARDT, C. (1965), Angew. Chem., Int. Ed. Engl., 4, 29-40. solvent parameter

REICHARDT, C. (1988), "Solvents and Solvent Effects in Organic Chemistry" 2nd ed., VCH Verlagsgesellschaft, Weinheim, Chap. 7. Dimroth-Reichardt ET parameter, polarity, solvent parameter, solvatochromism, polarity

REICHARDT, C., ASHARIN-FARD, S., and SCHÄFER, G. (1993), Chem. Ber., 126, 143-147. halochromism

REYNOLDS, W. F., and TOPSOM, R. D. (1984), J. Org. Chem., 49, 1989-1992. Swain-Lupton equation

RITCHIE, C. D. (1972), Acc. Chem. Res., 5, 348-354. Ritchie equation

RITCHIE, C. D. (1978), Pure Appl Chem., 50, 1281-1290. Ritchie equation

RITCHIE, C. D. (1986), Can. J. Chem., 64, 2239-2250. Ritchie equation

ROCHESTER, C. H. (1970), "Acidity Functions", Academic Press, New York. acidity function

ROSS, J. A., SEIDERS, R. P., and LEMAL, D. M. (1976), J. Am. Chem. Soc., 98, 4325-4327. pseudopericyclic

SALEM, L. (1971), Acc. Chem. Res., 4, 322-328. narcissistic reaction

SAYTZEFF, A. (1875), Justus Liebigs Ann. Chem., 179, 296-301. Saytzeff rule

SCHLESENER, C. J., AMATORE, C., and KOCHI, J. K. (1986), J. Phys. Chem., 90, 3747-3756. intrinsic barrier

SEEBACH, D. (1979), Angew. Chem., Int. Ed. Engl., 18, 239-258. umpolung

SEEMAN, J. I. (1983), Chem. Rev., 83, 83-134. Curtin-Hammett principle

SEEMAN, J. I., SECOR, H. V., HARTUNG, H., and GALZERANO, R. (1980), J. Am. Chem. Soc., 102, 7741-7747. Curtin-Hammett principle

SHORTER, J. (1973), "Correlation Analysis in Organic Chemistry: An Introduction to Linear Free Energy Relationships", Oxford University Press. [sigma]-constant, Yukawa-Tsuno equation

SIEHL, H.-U. (1987), Adv. Phys. Org. Chem., 23, 63-163. isotopic perturbation, method of

SMITH, P. A. S., and DeWALL, G. L. (1977), J. Am. Chem. Soc., 99, 5751-5760. ambident

STEWART, G. W., and MORROW, R. M. (1927), Proc. Natl. Acad. Sci. USA, 13, 222-223. cybotactic region

STOCK, L. M., and BROWN, H. C. (1963), Adv. Phys. Org. Chem., 1, 35-154. partial rate factor, reactivity-selectivity principle, selectivity factor

SUSTMANN, R., and KORTH, H.-G. (1990), Adv. Phys. Org. Chem., 26, 131-178. captodative effect

SWAIN, C. G. (1984), J. Org. Chem., 49, 2005-2010. Swain-Lupton equation

SWAIN. C. G., and LUPTON, E. C. (1968), J. Am. Chem. Soc., 90, 4328-4337. Swain-Lupton equation

SWAIN, C. G., and SCOTT, C. B. (1953), J. Am. Chem. Soc., 75, 141-147. Swain-Scott equation

SWAIN, C. G., UNGER, S. H., ROSENQUIST, N. R., and SWAIN, M. S. (1983), J. Am. Chem. Soc., 105, 492-502. Swain-Lupton equation

TAFT, R. W., Jr. (1952, 1953), J. Am. Chem. Soc., 74, 3120-3128; 75, 4231-4238. Taft equation

TAFT, R. W., Jr., and TOPSOM, R. D. (1987), Progr. Phys. Org. Chem., 16, 1-83. dual substituent parameter equation, electromeric effect, inductive effect, inductomeric effect, polarizability

THORNTON, E. R., (1967), J. Am. Chem. Soc., 89, 2915-2927. reacting bond rules

TISLER, M. (1973), Synthesis, 123-136. valence tautomerism

TROST, B. M. (1980), Acc. Chem. Res., 13, 385-393. chemoselective, chemoselectivity

VIEHE, H. G., JANOUSEK, Z., MERËNY, R., and STELLA, L. (1985), Acc. Chem. Res., 18, 148-154. captodative effect

WEBER, A., and VÖGTLE, F. (1980), Inorg. Chim. Acta, 45, L65-L67. cryptand

WILLIAMS, A. (1984), Acc. Chem. Res., 17, 425-430. effective charge, Hammond principle

WILLIAMS, A. (1992), Adv. Phys. Org. Chem., 27, 1-55. effective charge

WINEY, D. A., and THORNTON, E. R. (1975), J. Am. Chem. Soc., 97, 3102-3108. More O'Ferrall-Jencks diagram

WINSTEIN, S., GRUNWALD, E., and JONES, H. W. (1951), J. Am. Chem. Soc., 73, 2700-2707. Grunwald-Winstein equation

WISEMAN, J. R. (1967), J. Am. Chem. Soc., 89, 5966-5968. Bredt's rule

WISEMAN, J. R., and CHONG, J. A. (1969), J. Am. Chem. Soc., 91, 7775-7777. Bredt's rule

WITT, O. N. (1876), Ber. Deut. Chem. Ges., 9, 522-527. chromophore

WOODWARD, R. B., and HOFFMANN, R. (1969), Angew. Chem., Int. Ed. Engl., 8, 781-853. cheletropic reaction, cycloaddition, orbital symmetry

WOLFSBERG, M. (1972), Acc. Chem. Res., 5, 225-233. isotope effect, kinetic and thermodynamic

YATES, B. F., BOUMA, W. J., and RADOM, L. (1986), Tetrahedron, 42, 6225-6234. distonic radical cation

YUKAWA. Y., and TSUNO, Y. (1959), Bull. Chem. Soc. Jpn, 32, 971-981. Yukawa-Tsuno equation

ZIMMERMAN, H. E. (1971), Acc. Chem. Res., 4, 272-280. aromatic, Möbius aromaticity


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