'A' value
Term · Chemistry · MLC-T-CHM-000027
A measure of the conformational preference of a substituent on a cyclohexane ring, representing the difference in Gibbs free energy between the axial and equatorial positions. A larger 'A' value indicates a stronger preference for the equatorial position due to steric hindrance in the axial orientation. These values are typically determined experimentally using nuclear magnetic resonance spectroscopy or computational methods.
| Identifier | MLC-T-CHM-000027 |
|---|---|
| Field | Chemistry |
| Subject | Organic and Biomolecular Chemistry |
| Synonyms | Winstein-Holness A value |
| References | PAC, 1994, 66, 1077. 'Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)' on page 1087 (https://doi.org/10.1351/pac199466051077) |
| See also | Equatorial; Equilibration |
Record as JSON
{
"id": "MLC-T-CHM-000027",
"term": "'A' value",
"field": "Chemistry",
"definition": "A measure of the conformational preference of a substituent on a cyclohexane ring, representing the difference in Gibbs free energy between the axial and equatorial positions. A larger 'A' value indicates a stronger preference for the equatorial position due to steric hindrance in the axial orientation. These values are typically determined experimentally using nuclear magnetic resonance spectroscopy or computational methods.",
"synonyms": [
"Winstein-Holness A value"
],
"subject": "Organic and Biomolecular Chemistry",
"see_also": [
"equatorial",
"equilibration"
],
"references": [
"PAC, 1994, 66, 1077. 'Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)' on page 1087 (https://doi.org/10.1351/pac199466051077)"
],
"url": "https://mlchart.com/terminology/chemistry/a-value/"
}
Record 27 of 13,676 in Chemistry terminology (MLC-0109). Request the full dataset.