Nomenclature of Organic Chemistry IUPAC Recommendations and Preferred Names 2013¶
IUPAC. (2013). Nomenclature of Organic Chemistry IUPAC Recommendations and Preferred Names 2013.
Cited by¶
1 citation across 1 artifact.
Each citation links to the sentence it supports in the citing article.
Domain-specific¶
- Cis–Trans Isomerism
- The IUPAC Blue Book gives cis-but-2-ene as (2Z)-but-2-ene and trans-but-2-ene as (2E)-but-2-ene; its preferred names use E/Z, while cis/trans has a restricted general-nomenclature use for these double-bond examples.
This sourceLinked title transcribes the printed colon after “Chemistry” without punctuation for reference-key parsing. Full IUPAC-hosted chapter with paired but-2-ene examples and conformer warning.
- The IUPAC Blue Book gives cis-but-2-ene as (2Z)-but-2-ene and trans-but-2-ene as (2E)-but-2-ene; its preferred names use E/Z, while cis/trans has a restricted general-nomenclature use for these double-bond examples.
Verification¶
Does it exist? Not checked yet. This entry carries no identifier to resolve. It was extracted from the citation as written in the article, normalized, and deduplicated against the rest of the registry.
Does it back the claim? Not recorded. The single citation of this work carries no recorded support check.
Support is checked per citation rather than per work — the same source can be cited soundly in one article and wrongly in another. Per-citation recording began recently, so a citation with no recorded check is a gap in the record rather than evidence it went unchecked.
See how references were verified.
Registry ID ref:0965d1c27a4b · see in the full table