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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.

Contributors 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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