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Physical organic chemistry
Physical organic chemistry is the study of the interrelationships between structure and reactivity in organic molecules. It a part of organic chemistry by using tools of physical chemistry such as chemical equilibrium, chemical kinetics, thermochemistry, and quantum chemistry.
Industry: Chemistry
Add a new termContributors in Physical organic chemistry
Physical organic chemistry
enforced concerted mechanism
Chemistry; Physical organic chemistry
Variation of reaction parameters in a series of reactions proceeding in non-concerted steps may lead to a situation, where the putative intermediate will possess a lifetime shorter than a bond ...
entering group
Chemistry; Physical organic chemistry
An atom or group that forms a bond to what is considered to be the main part of the substrate during a reaction. For example: the attacking nucleophile in a bimolecular nucleophilic substitution ...
enthalpy of activation
Chemistry; Physical organic chemistry
The standard enthalpy difference between the transition state and the ground state of the reactants at the same temperature and pressure. It is related to the temperature coefficient of the rate ...
standard entalpy of activation
Chemistry; Physical organic chemistry
The standard enthalpy difference between the transition state and the ground state of the reactants at the same temperature and pressure. It is related to the temperature coefficient of the rate ...
entropy of activation
Chemistry; Physical organic chemistry
The standard entropy difference between the transition state and the ground state of the reactants, at the same temperature and pressure. It is related to the Gibbs energy of activation and enthalpy ...
standard entropy of activation
Chemistry; Physical organic chemistry
The standard entropy difference between the transition state and the ground state of the reactants, at the same temperature and pressure. It is related to the Gibbs energy of activation and enthalpy ...
epimer
Chemistry; Physical organic chemistry
A diastereoisomer that has the opposite configuration at only one of two or more tetrahedral "stereogenic" centers present in the respective molecular entity.
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