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In [[organic chemistry]], the term '''acetylenic''' designates [[Category:Organic chemistry]] ...

...ly-used<ref name=":0"/> term in acid-base chemistry|the meaning in organic chemistry|Conjugated system#Mechanism}} ...Homoassociation| file = H02842}}</ref> is an association between a [[base (chemistry)|base]] and its [[conjugate acid]] through a [[hydrogen bond]].<ref name=": ...

{{Short description|Organic compounds of the form R3–Si–OH}} ...etschnig, Stefan Spirk|periodical=Coordination Chemistry Reviews|title=The Chemistry of Organo Silanetriols|volume=323|year=2016|pages=87–106|language=en|doi=10 ...

...r of atoms.<ref>{{cite book |title= The Vocabulary And Concepts Of Organic Chemistry|last= Orchin|first=Milton |year= 2005|publisher= John Wiley & Sons |isbn= 9 ...rties:<ref name=Jones>{{cite book |title= Physical and Mechanistic Organic Chemistry|last= Yardley Jones|first=Richard Arnold |year= 1979|publisher= Cambridge U ...

...047084289X.ra026|chapter=Acetyl Cyanide|title=Encyclopedia of Reagents for Organic Synthesis|year=2001|last1=Morris|first1=Joel|isbn=0471936235}}</ref> ...[[carboxylate]]:<ref>{{cite journal |doi=10.1002/anie.198200361|title=The Chemistry of Acyl Cyanides|year=1982|last1=Hünig|first1=Siegfried|last2=Schaller|firs ...

|Type = Organic redox reaction The '''Fukuyama reduction''' is an [[organic reaction]] and an [[organic reduction]] in which a [[thioester]] is reduced to an [[aldehyde]] by a [[s ...

In [[chemistry]], a '''quaternary compound''' is a compound consisting of exactly four che ...itively charged atom with four substituents, especially [[organic compound|organic]] ([[alkyl]] and [[aryl]]) groups, discounting [[hydrogen]] atoms.<ref>{{Go ...

...anic substrate. The method is used in the [[organic synthesis|synthesis of organic compounds]].<ref name=Ullmann>{{Ullmann|doi=10.1002/14356007.a02_001|title= ...eophiles to [[acrylonitrile]]. Typical protic nucleophiles are [[alcohol (chemistry)|alcohol]]s, [[thiol]]s, and [[amine]]s. Two new bonds form: C-H and C-X ( ...

...chem>|caption=Example of a dipolar compound, represented by a [[Resonance (chemistry)|resonance structure]] ([[isocyanide]])}} In [[organic chemistry]], a '''dipolar compound''' or simply '''dipole''' is an electrically neutr ...

...resonance effects in electrophilic reactions of para- and meta-substituted organic compounds. This equation does so by introducing a new term to the original ...uch effects.<ref name=AD>Anslyn E, Dougherty DA. ''Modern Physical Organic Chemistry''. University Science Books, 2006, p 456.</ref> ...

...}}.</ref> It is often used in [[chemoinformatics]] for investigations of [[organic compound]]s. |journal=MATCH Communications in Mathematical and in Computer Chemistry ...

{{short description|Organic reaction between amine and alkyl halide}} '''Amine alkylation''' ('''amino-dehalogenation''') is a type of [[organic reaction]] between an [[alkyl halide]] and [[ammonia]] or an [[amine]].<ref ...

...ydride transfer in Podophyllum peltatum | journal = Organic & Biomolecular Chemistry | volume = 4 | issue = 5 | pages = 808–16 | date = March 2006 | pmid = 1649 ...

{{Short description|Israeli organic chemist (1930–2024)}} | field = [[Chemical synthesis|Synthetic organic chemistry]], [[Heterocyclic compound|Heterocycles]] ...

...resence of the old yellow enzyme FgaOx3 | journal = Organic & Biomolecular Chemistry | volume = 8 | issue = 15 | pages = 3500–8 | date = August 2010 | pmid = 20 ...

{{short description|Organic compounds of the form B(OR)₃ or B₃O₃(OR)₃}} ...stoichiometric [[condensation reaction]] of [[boric acid]] with [[Alcohol (chemistry)|alcohols]]. There are two main classes of borate [[ester]]s: [[Orthoborate ...

...|last2= Grein |first3= Jack |last3= Passmore |journal= Canadian Journal of Chemistry |volume= 89 |issue= 6 |year= 2011 |pages= 671–687 |doi= 10.1139/v11-039 }}< ...

...a novel streptomyces diterpene cyclase | journal = The Journal of Organic Chemistry | volume = 68 | issue = 14 | pages = 5433–8 | date = July 2003 | pmid = 128 ...

...ions such as the [[nitration]] of conjugated systems from a [[Theoretical chemistry|theoretical perspective]]. ...lting in the equation:<ref>{{cite book |title=Progress in Physical Organic Chemistry |volume=2|last= Cohen|first= Saul |author2=Andrew Streitwieser |author3=Rob ...

== [[IUPAC nomenclature of chemistry|IUPAC]] Name* == == CAS Common Chemistry<ref>{{Cite web |title=CAS Common Chemistry |url=https://commonchemistry.cas.org/detail?cas_rn=7432-28-2}}</ref><ref>{{ ...