Donald W Rogers MA
Psychologist | Clinical
203 North Main Street Stanton KY, 40380About
Dr. Donald Rogers is a psychologist practicing in Stanton, KY. Dr. Rogers specializes in the treatment of mental health problems, and helps people to cope with their mental illnesses. As a psychologist, Dr. Rogers evaluates and treats patients through a variety of methods, most typically being psychotherapy or talk therapy. Patients usually visit Dr. Rogers because they have been experiencing depression, anxiety, stress or anger for a significant period of time and are seeking help. Psychologists may perform a variety of exams and assessments to diagnose a mental condition.
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Expert Publications
Data provided by the National Library of Medicine- The aromaticity of pyracylene: an experimental and computational study of the energetics of the hydrogenation of acenaphthylene and pyracylene.
- Pauling's electronegativity equation and a new corollary accurately predict bond dissociation enthalpies and enhance current understanding of the nature of the chemical bond.
- The conjugation stabilization of 1,3-butadiyne is zero.
- On the lack of conjugation stabilization in polyynes (polyacetylenes).
- G3(MP2) enthalpies of hydrogenation, isomerization, and formation of extended linear polyacetylenes.
- Stabilization energies of extensively conjugated propargylic radicals.
- Remote substituent effects on allylic and benzylic bond dissociation energies. Effects on stabilization of parent molecules and radicals.
- Enthalpies of formation of hydrocarbons by hydrogen atom counting. Theoretical implications.
- Effects of molecule stabilization energies on radical reactions: G3 and G3(MP2) model chemistries applied to benzylic systems.
- Shortcomings of basing radical stabilization energies on bond dissociation energies of alkyl groups to hydrogen.
- Heats of formation of organic compounds by a simple calculation.
- Electrophilic aromatic substitution: enthalpies of hydrogenation of the ring determine reactivities of C6H5X. The direction of the C6H5-X bond dipole determines orientation of the substitution.
- Electrophilic Addition to Alkenes: The Relation between Reactivity and Enthalpy of Hydrogenation: Regioselectivity is Determined by the Stability of the Two Conceivable Products.
- Long Chain Saturated and Unsaturated Carboxylic Acids: Filling a Large Gap of Knowledge in Their Enthalpies of Formation.
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