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|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 ...

...the widely-used<ref name=":0"/> term in acid-base chemistry|the meaning in organic chemistry|Conjugated system#Mechanism}} ...ity Scale of Neutral Brønsted Acids in Acetonitrile|journal=The Journal of Organic Chemistry|date=March 2006|volume=71|issue=7|pages=2829–2838|doi=10.1021/jo0 ...

...ygen]] atoms. That is, they are the [[conjugate base]]s of '''polycarbonic acids''', the conceptual [[anhydride]]s of [[carbonic acid]], or polymers of [[ca ...ut stabilized when paired with metal [[counterion]]s or as their conjugate acids.<ref>{{cite journal |title= Density functional theory (DFT) calculations on ...

...This expectation explains extensive search for better NLO materials among organic crystals. ...ological substances. It forms a number of salts with organic and inorganic acids showing non-linear optical properties. L-Arginine maleate dihydrate (C<sub> ...

{{short description|Organic compounds of the form B(OR)₃ or B₃O₃(OR)₃}} In [[organic chemistry]], '''borate esters''' are [[organoboron compound]]s which are co ...

{{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 ...

...licate]] anions, which are their better known [[conjugate base]]s, silicic acids are proposed to be [[oligomer]]ic or [[polymer]]ic. No [[Monomer|simple]] s ...nd polysilicic (di-, tri-, tetrasilicic, etc.) acids. Well defined silicic acids have not been obtained in a form that has been characterized by [[X-ray cry ...

In [[organic chemistry]], a '''nitrate ester''' is an organic [[functional group]] with the formula {{chem2|R\sONO2}}, where R stands for Most commonly, "mixed acid" (nitric and sulfuric acids) are used, but in the 1980s production of the [[nitrocellulose]] with [[mag ...

...nol|alcohol]], [[acetonitrile]], [[dimethylformamide]] and most of polar [[organic solvents]] ...ct of the three fluorine atoms adjacent the [[carboxylate group]]. Strong acids such as [[hydrochloric acid]] or [[sulfuric acid]] can protonate the triflu ...

...2693–2698|doi=10.1021/ja00528a029|title=Divalent lanthanide derivatives in organic synthesis. 1. Mild preparation of samarium iodide and ytterbium iodide and ...water to produce hydrogen gas and basic iodides, and reacts violently with acids.<ref name="Yb_1931"/> Ytterbium(II) iodide sinters at 0.01&nbsp;Torr from a ...

{{Short description|Abnormality of the human body's normal balance of acids and bases}} ...abnormality of the human body's normal [[acid–base homeostasis|balance of acids and bases]] that causes the [[blood plasma|plasma]] [[pH]] to deviate out o ...

{{Acids and bases}} The strength of a weak [[organic chemistry|organic]] acid may depend on substituent effects. The strength of an [[inorganic ch ...

The '''Edwards equation''' in organic chemistry is a two-parameter equation for correlating [[nucleophile|nucleop ...rroll | first = Felix | title = Perspectives on Structure and Mechanism in Organic Chemistry | publisher = Wiley | edition = 2 | date = 2010 | location = New ...

...cott D. Rychnovsky, Jay P. Powers | title = [[Encyclopedia of Reagents for Organic Synthesis]] | year = 2001 | doi = 10.1002/047084289X.rz011 | chapter = Zinc ...he physical state of the zinc (e.g. powder or granules), the use of protic acids and other additives, and temperature of the preparation. Most often the co ...

...their composition. Organic carbon forms the backbone of key components of organic compounds such as [[protein]]s, [[lipid]]s, [[carbohydrate]]s, and [[nuclei ...|right|Carbon is separated into four distinct pools based on whether it is organic or inorganic, and whether it is dissolved or particulate. The processes ass ...

...ents including, [[benzene]]. It is a [[reagent]] used in the synthesis of organic and inorganic triflates. .... Perfluoroalkyl derivatives of sulphur. Part IV. Perfluoroalkanesulphonic acids|pages=173–180|date=1956|language=German|doi=10.1039/JR9560000173}}</ref> ...

...MPA(MoOPH): 3-HYDROXY-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPTAN-2-ONE| journal = Organic Syntheses| volume = 64| pages = 127| year = 1986}}</ref> Other reagents use ...of &alpha;-hydroxycarbonyl compounds from enolates|journal=The Journal of Organic Chemistry|volume=43|issue=2|pages=188–196|doi=10.1021/jo00396a002|issn=0022 ...

...osition involves the breakdown of proteins, carbohydrates, lipids, nucleic acids, and bone. *[[amino acids]] ...

...na | last3 = García-Blanco | first3 = Francisco | journal = The Journal of Organic Chemistry | volume = 64 | issue = 17 | pages = 6512–6514}}</ref> ...Benzoicacid.png|thumbnail|right|300px |Dissociation of substituted benzoic acids.]] ...

...ctivity relationship|quantitative structure activity relationships]] for [[organic compound]]s. It was developed by C. Gardner Swain and Elmer C. Lupton Jr. In organic chemistry, the Hammett plot provides a means to assess [[substituent]] effe ...