Unimolecular reactions and energy partitioning. Three- and four-centered elimination reactions of chemically activated 1,1,2-trichloroethane-d0-d1, and -d2

K. C. Kim; D. W. Setser

doi:10.1021/j100614a018

Unimolecular reactions and energy partitioning. Three- and four-centered elimination reactions of chemically activated 1,1,2-trichloroethane-d0-d1, and -d2

The Journal of Physical Chemistry ◽

10.1021/j100614a018 ◽

1974 ◽

Vol 78 (21) ◽

pp. 2166-2179 ◽

Cited By ~ 36

Author(s):

K. C. Kim ◽

D. W. Setser

Keyword(s):

Energy Partitioning ◽

Unimolecular Reactions ◽

Elimination Reactions

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Comparison of energy partitioning from three-centered processes. Bimolecular transfer and unimolecular elimination reactions

The Journal of Physical Chemistry ◽

10.1021/j100682a029 ◽

1971 ◽

Vol 75 (13) ◽

pp. 2070-2072 ◽

Cited By ~ 14

Author(s):

D. W. Setser ◽

H. W. Chang ◽

M. J. Perona

Keyword(s):

Energy Partitioning ◽

Elimination Reactions

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Rate constants, threshold energies, and energy partitioning for three and four centered hydrogen chloride elimination reactions of 1,1,2-trichloroethane-1-d1

The Journal of Physical Chemistry ◽

10.1021/j100646a025 ◽

1972 ◽

Vol 76 (2) ◽

pp. 283-284 ◽

Cited By ~ 16

Author(s):

K. C. Kim ◽

D. W. Setser

Keyword(s):

Hydrogen Chloride ◽

Rate Constants ◽

Energy Partitioning ◽

Elimination Reactions ◽

Chloride Elimination ◽

Threshold Energies

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Contributions of parent molecule fixed and excess energies to product energy partitioning in four-center elimination reactions

Chemical Physics Letters ◽

10.1016/0009-2614(89)87175-1 ◽

1989 ◽

Vol 155 (4-5) ◽

pp. 391-398 ◽

Cited By ~ 3

Author(s):

R.M. Benito ◽

J. Santamaría

Keyword(s):

Energy Partitioning ◽

Parent Molecule ◽

Elimination Reactions

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The Unimolecular Reactions of CF3CHF2 Studied by Chemical Activation: Assignment of Rate Constants and Threshold Energies to the 1,2-H Atom Transfer, 1,1-HF and 1,2-HF Elimination Reactions, and the Dependence of Threshold Energies on the Number of F-Atom Substituents in the Fluoroethane Molecules

The Journal of Physical Chemistry A ◽

10.1021/acs.jpca.7b06769 ◽

2017 ◽

Vol 121 (46) ◽

pp. 8746-8756 ◽

Cited By ~ 3

Author(s):

Caleb A. Smith ◽

Blanton R. Gillespie ◽

George L. Heard ◽

D. W. Setser ◽

Bert E. Holmes

Keyword(s):

Rate Constants ◽

Chemical Activation ◽

Atom Transfer ◽

Unimolecular Reactions ◽

Elimination Reactions ◽

Threshold Energies

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The Quantum Theory of Unimolecular Reactions

10.1017/cbo9780511735837 ◽

1984 ◽

Cited By ~ 20

Author(s):

H. O. Pritchard

Keyword(s):

Quantum Theory ◽

Unimolecular Reactions

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CHEMCompete-II: Chemistry card game for substitution and elimination reactions of alcohols

10.1021/scimeetings.0c01430 ◽

2020 ◽

Author(s):

Deana Jaber ◽

Maria Camarca ◽

William Heuett

Keyword(s):

Card Game ◽

Elimination Reactions

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Intramolecular interactions in N-methylsalicylaldimine and its anion. A semi-empirical energy partitioning analysis

Journal de Chimie Physique ◽

10.1051/jcp/1981780127 ◽

1981 ◽

Vol 78 ◽

pp. 127-130 ◽

Cited By ~ 4

Author(s):

Salavatore Millefiori ◽

Arcangelo Millefiori

Keyword(s):

Energy Partitioning ◽

Intramolecular Interactions ◽

Semi Empirical

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Part I. Comparison of 1,2- and 1,3- elimination reactions; Part II. Factors which influence the ionization of carboxylic acids

10.31274/rtd-180813-15319 ◽

1954 ◽

Author(s):

Donald H. Hogle

Keyword(s):

Carboxylic Acids ◽

Elimination Reactions

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Double resonance reactant preparation for state-to-state studies of unimolecular reactions: Progress report, August 15, 1988--August 14,1989

10.2172/6321105 ◽

1989 ◽

Author(s):

T. R. Rizzo

Keyword(s):

Double Resonance ◽

Progress Report ◽

Unimolecular Reactions

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Solvolytic reactions of empiric 3-methanesulfonyloxy-7-benzoyloxy-5β,6β-cyclopropanocholestanes

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19860436 ◽

1986 ◽

Vol 51 (2) ◽

pp. 436-446 ◽

Cited By ~ 1

Author(s):

Ladislav Kohout ◽

Vijay Kumar Sethi ◽

Jaroslav Zajíček ◽

Alexander Kasal

Keyword(s):

Spectral Methods ◽

Elimination Reactions

Acetolysis of 3-methanesulfonyloxy-7-benzoyloxy-5β,6β-cyclopropanocholestanes with various configurations in positions 3 and 7 is described and the products are assigned structure using spectral methods. The 7-substituted compounds show greater propensity to elimination reactions than the 7-unsubstituted ones.

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