benzile Sentence Examples
- The benzile molecule exhibits a unique planar structure due to its symmetrical arrangement of benzene rings.
- Benzile is employed as an intermediate in the synthesis of various organic compounds, such as dyes and pharmaceuticals.
- The distinctive pale yellow color of benzile is attributed to the presence of an extended conjugated system.
- Benzile undergoes electrophilic aromatic substitution reactions readily due to the electron-withdrawing effect of the ketone groups.
- The reduction of benzile yields hydrobenzoin, which finds applications in the production of fine chemicals.
- Benzile has been investigated for its potential use as a photoinitiator in free radical polymerization processes.
- The crystallographic data reveals that benzile molecules pack together in an orthorhombic lattice with a space group of Pbca.
- Benzile exhibits a strong absorption band in the ultraviolet region of the electromagnetic spectrum, corresponding to its π-π* transition.
- The solubility of benzile in organic solvents is limited due to its polar nature and extended molecular size.
- Benzile has been extensively studied for its biological activity, including its antioxidant and anti-inflammatory properties.
benzile Meaning
benzile (n.)
A yellowish crystalline substance, C6H5.CO.CO.C6H5, formed from benzoin by the action of oxidizing agents, and consisting of a doubled benzoyl radical.
Synonyms & Antonyms of benzile
No Synonyms and anytonyms found
FAQs About the word benzile
A yellowish crystalline substance, C6H5.CO.CO.C6H5, formed from benzoin by the action of oxidizing agents, and consisting of a doubled benzoyl radical.
No synonyms found.
No antonyms found.
The benzile molecule exhibits a unique planar structure due to its symmetrical arrangement of benzene rings.
Benzile is employed as an intermediate in the synthesis of various organic compounds, such as dyes and pharmaceuticals.
The distinctive pale yellow color of benzile is attributed to the presence of an extended conjugated system.
Benzile undergoes electrophilic aromatic substitution reactions readily due to the electron-withdrawing effect of the ketone groups.
