Related Experiment Video
Updated: Jun 5, 2026

Microwave-assisted Functionalization of Poly(ethylene glycol) and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation
Published on: October 29, 2013
2-Methyl-3-(3-methyl-phen-yl)acrylic acid.
This study reveals the crystal structure of C(11)H(12)O(2), detailing how molecules form dimers via hydrogen bonds. These dimers further connect through specific C-H⋯O and π-π interactions, influencing crystal packing.
Area of Science:
- Crystallography
- Supramolecular Chemistry
Background:
- Understanding molecular interactions is crucial for materials science.
- Crystal structure analysis provides insights into intermolecular forces.
Purpose of the Study:
- To elucidate the crystal structure of C(11)H(12)O(2).
- To identify and characterize the intermolecular interactions governing crystal packing.
Main Methods:
- Single-crystal X-ray diffraction was employed to determine the crystal structure.
- Analysis of hydrogen bonds (O-H⋯O, C-H⋯O) and π-π interactions was performed.
Main Results:
- The crystal structure features dimers formed by O-H⋯O hydrogen bonds.
- Dimers are linked by C-H⋯O hydrogen bonds, creating five-membered rings.
- Two distinct π-π interactions with perpendicular distances of 3.006 and 3.396 Å were observed, alongside C-H⋯π and C-O⋯π interactions.
Conclusions:
- The crystal packing of C(11)H(12)O(2) is dictated by a combination of hydrogen bonding and π-π stacking.
- These interactions define the supramolecular architecture of the compound.
Related Concept Videos
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Nomenclature of Carboxylic Acid Derivatives: Acid Halides, Esters, and Acid Anhydrides
The IUPAC and common names of acid halides are derived from the corresponding carboxylic acids, by changing “ic acid” to “yl halide.” For example, as shown below, the IUPAC name ethanoyl chloride is derived from ethanoic acid, and the common name, acetyl chloride, is obtained from acetic acid.
IUPAC Nomenclature of Aldehydes
IUPAC Nomenclature of Carboxylic Acids
For acyclic saturated monocarboxylic acids, the longest hydrocarbon chain containing the –COOH carbon is identified as the parent chain. Then, the last -e of the parent hydrocarbon name is replaced with a suffix -oic acid.
Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives
Carboxylic Acids to Methylesters: Alkylation using Diazomethane

