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  • ...te, which is the conjugate base of [[benzoic acid]]. [[Acetic acid]] is a carboxylic acid that gives vinegar its bite. [[Formic acid]] has historically been used to ...Conversely, the [[Fisher esterification]] reaction can be used to react a carboxylic acid with an alcohol to form an ester. Carboxylic acids can also be reduced to f
    2 KB (398 words) - 15:31, 8 March 2023
  • 12 bytes (1 word) - 16:43, 4 December 2007
  • 101 bytes (15 words) - 18:06, 17 July 2008
  • Auto-populated based on [[Special:WhatLinksHere/Carboxylic acid]]. Needs checking by a human.
    681 bytes (92 words) - 11:40, 11 January 2010
  • 29 bytes (3 words) - 12:47, 4 July 2009

Page text matches

  • ...d''', HCOOH, also known as methanoic acid, is the simplest member of the [[carboxylic acid]]s, RCOOH (where R = H, or any alkyl group). It is a pungent liquid which i Formic acid is a stronger acid than any other member of the unsubstituted carboxylic acid series, and forms salts, called formates, which (except for those of lead a
    613 bytes (100 words) - 15:10, 12 April 2008
  • An omega-3 fatty acid consisting of a carboxylic acid with a 22-carbon chain, and six cis double bonds.
    140 bytes (21 words) - 10:07, 3 September 2009
  • <noinclude>{{Subpages}}</noinclude>Carboxylic acid form of vitamin A, also known as all-trans retinoic acid or ATRA, is a topi
    198 bytes (30 words) - 09:28, 28 November 2013
  • * trans-4-aminomethylcyclohexane-1-carboxylic acid
    563 bytes (50 words) - 17:33, 22 October 2010
  • A [[dehydration reagent]] used to couple [[carboxylic acid]]s with [[alohol]]s or [[amine]]s.
    129 bytes (18 words) - 11:05, 3 October 2009
  • Chemical used to synthesize activated, semi-stable [[carboxylic acid]] [[esters]] for subsequent coupling reactions.
    152 bytes (16 words) - 09:29, 7 October 2009
  • ...te, which is the conjugate base of [[benzoic acid]]. [[Acetic acid]] is a carboxylic acid that gives vinegar its bite. [[Formic acid]] has historically been used to ...Conversely, the [[Fisher esterification]] reaction can be used to react a carboxylic acid with an alcohol to form an ester. Carboxylic acids can also be reduced to f
    2 KB (398 words) - 15:31, 8 March 2023
  • ...s closely related to the acidic amino acid [[glutamic acid]] which has a [[carboxylic acid]] in place of the amide group present in glutamine. Glutamine is a neutral
    547 bytes (87 words) - 08:08, 8 June 2009
  • A [[carbodiimide]] used to activate [[carboxylic acid]]s for coupling with [[alcohol]]s or [[amine]]s.
    138 bytes (19 words) - 11:33, 3 October 2009
  • Dehydrating chemical mostly used to couple [[carboxylic acid]]s with primary [[amine]]s, producing an [[amide]] compound.
    157 bytes (20 words) - 10:36, 3 October 2009
  • A [[carbodiimide]] reagent mostly used to activate [[carboxylic acid]]s for coupling with [[alcohol]]s or [[amine]]s.
    153 bytes (21 words) - 10:31, 3 October 2009
  • ...NHS) is chemical used to form semi-stable, but reactive, [[ester]]s from [[carboxylic acid]]s. Such NHS esters can be stored for a relatively long time if kept cold a ...diimide coupling via NHS ester.png|left|350px|'''Scheme 1''':Coupling of a carboxylic acid and a primary amine via O-acylisourea ester and NHS ester intermediates.}}
    1 KB (235 words) - 10:55, 9 January 2010
  • Auto-populated based on [[Special:WhatLinksHere/Carboxylic acid]]. Needs checking by a human.
    681 bytes (92 words) - 11:40, 11 January 2010
  • HCO<sub>2</sub>H, the smallest [[carboxylic acid]], and the sting delivered by stinging [[nettle]]s and [[ant]]s.
    149 bytes (22 words) - 11:14, 13 July 2008
  • ...c acid''', formula CH<sub>3</sub>CO<sub>2</sub>H, is the second smallest [[carboxylic acid]] and is larger than only [[formic acid]], HCO<sub>2</sub>H. Vinegar's tar
    832 bytes (128 words) - 08:12, 15 March 2024
  • {{r|Carboxylic acid}}
    545 bytes (73 words) - 16:37, 11 January 2010
  • {{r|carboxylic acid}}
    178 bytes (23 words) - 16:09, 4 November 2010
  • '''N,N'-dicyclohexylcarbodiimide''' is carbodiimide reagent used to couple [[carboxylic acid]]s with either [[alcohol]]s or [[amine]]s to form [[ester]]s or [[amide]]s.
    288 bytes (35 words) - 11:03, 3 October 2009
  • ...rred to as an [[amino acid]] despite the fact that it does not contain a [[carboxylic acid]] group like most amino acids do. It plays an important role in the phase
    3 KB (353 words) - 11:31, 11 December 2010
  • ...into the carbonyl system. This makes the carbonyl less reactive than most carboxylic acid derivatives in [[electrophile|electrophilic]] substitution reactions, and m *Reaction of most other [[carboxylic acid]] derivatives with ammonia, a primary amine, or a secondary amine will give
    3 KB (410 words) - 02:51, 17 October 2013
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