MLchartDataset catalogue

'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.

Table 1. Record
IdentifierMLC-T-CHM-000027
FieldChemistry
SubjectOrganic and Biomolecular Chemistry
SynonymsWinstein-Holness A value
ReferencesPAC, 1994, 66, 1077. 'Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)' on page 1087 (https://doi.org/10.1351/pac199466051077)
See alsoEquatorial; 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.