1996Acta Crystallographica Section C Crystal Structure CommunicationsRequires access

(±)-trans-2-Benzoylcyclohexanecarboxylic Acid. Structure and Hydrogen-Bonding Pattern of a γ-Keto Acid

Roger A. Lalancette, M.L. Cote, H. W. Thompson

Open publisher page 0 citations

Abstract

In the title compound, C14H16O3, enantiomeric pairs of molecules form dimers by mutual hydrogen bonding of carboxyl groups, with the ketone group not involved in the hydrogen bonding. The components of the dimer differ in conformation, so that the dimer is the asymmetric unit.

About this research paper

What this paper is about

In the title compound, C14H16O3, enantiomeric pairs of molecules form dimers by mutual hydrogen bonding of carboxyl groups, with the ketone group not involved in the hydrogen bonding. The components of the dimer differ in conformation, so that the dimer is the asymmetric unit.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

In the title compound, C14H16O3, enantiomeric pairs of molecules form dimers by mutual hydrogen bonding of carboxyl groups, with the ketone group not involved in the hydrogen bonding. The components of the dimer differ in conformation, so that the dimer is the asymmetric unit.

Key concepts: Dimer, Hydrogen bond, Ketone, Molecule, Chemistry, Enantiomer, Group (periodic table), Hydrogen

Related papers

Back to paper searchBrowse research topicsOriginal source
(±)-trans-2-Benzoylcyclohexanecarboxylic Acid. Structure and Hydrogen-Bonding Pattern of a γ-Keto Acid — Research Paper | ScholarLens