Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

// request.cf · coarse context

A page that knows where it met you.

Only coarse request metadata is shown. This demo does not display or persist visitor IP addresses.

Country
US
Cloudflare location
CMH
Connection
HTTP/2
Language
Not provided

Ray ID: a241dcc58c34a0d6

Jump to content

Benzenoid

From Wikipedia, the free encyclopedia

In organic chemistry, benzenoids are a class of organic compounds with at least one benzene ring. These compounds have increased stability due to resonance in the benzene rings. Most aromatic hydrocarbons are benzenoid. Notable counterexamples are cyclooctadecanonaene, azulene and trans-bicalicene.[1][2]

See also

[edit]

References

[edit]
  1. Tomlinson, Muriel (1971). An Introduction to the Chemistry of Benzenoid Compounds (1st ed.). Elsevier. p. 207. doi:10.1016/C2013-0-10050-5. ISBN 978-0-08-015659-0.
  2. Tian, Jing-Pu; Ma, Zhi-Yao; Zhao, Kai-Ge; Zhang, Jie; Xiang, Lin; Chen, Long-Qing (September 14, 2018). "Transcriptomic and proteomic approaches to explore the differences in monoterpene and benzenoid biosynthesis between scented and unscented genotypes of wintersweet". Physiologia Plantarum. 166 (2): 478–493. doi:10.1111/ppl.12828. ISSN 1399-3054. PMID 30216458.