Crystal Structure of N-(2,3-Dimethylphenyl)succinamic Acid
Author Information
Author(s): Saraswathi B. S., Foro Sabine, Gowda B. Thimme, Fuess Hartmut
Primary Institution: Mangalore University
Hypothesis
The study investigates the effect of ring and side-chain substitutions on the crystal structures of anilides.
Conclusion
The crystal structure of N-(2,3-dimethylphenyl)succinamic acid shows specific conformations of its bonds and hydrogen bonding interactions.
Supporting Evidence
- The study determined the crystal structure of the compound using X-ray diffraction.
- The conformation of the amide hydrogen is syn to the ortho- and meta-methyl groups in the benzene ring.
- The molecules are linked into infinite chains through hydrogen bonds.
Takeaway
This study looks at how certain chemical groups affect the shape of a molecule, specifically a type of acid. It found that the way these groups are arranged can change how the molecule connects with others.
Methodology
The compound was synthesized from succinic anhydride and 2,3-dimethylaniline, followed by characterization using X-ray diffraction.
Digital Object Identifier (DOI)
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