FACTOID # 41: On the probability of not reaching 40 graph, the top 34 countries are all African.
 
 Home   Encyclopedia   Statistics   Countries A-Z   Flags   Maps   Education   Forum   FAQ   About 
 
WHAT'S NEW
RECENT ARTICLES
More Recent Articles »
 

SEARCH ALL

FACTS & STATISTICS    Advanced view

Search encyclopedia, statistics and forums:

 

 

(* = Graphable)

 

 


Encyclopedia > Fischer esterification

Fischer esterification is the process of forming an ester by refluxing a carboxylic acid and an alcohol in the presence of an acid (catalyst). This article is in need of attention. ... Reflux is a technique used in chemistry to apply energy to reactions over an extended period of time. ... Structure of a carboxylic acid Carboxylic acids, also known as alkanoic acids, are organic acids characterized by the presence of a carboxyl group and have the general chemical formula R-C(=O)-OH, also written as R-COOH, where R is a hydrogen or an alkyl group. ... In general usage, alcohol (from Arabic al-khwl الكحول, or al-ghawl الغول) refers almost always to ethanol, also known as grain alcohol, and often to any beverage that contains ethanol (see alcoholic beverage). ... An acid (often represented by the generic formula AH) is typically a water-soluble, sour-tasting chemical compound. ...


Acid catalysts

Commonly used acid catalysts for a Fischer esterification include:

Sulfuric acid (British English: sulphuric acid), H2SO4, is a strong mineral acid. ...

Mechanism

  1. Proton transfer from acid catalyst to carbonyl oxygen increases electrophilicity of carbonyl carbon.
  2. The carbonyl carbon is attacked by the nucleophilic oxygen atom of the alcohol.
  3. Formation of an oxonium ion.
  4. Proton transfer from the oxonium ion to a second molecule of alcohol gives a TCAC
  5. Proton transfer from one of the hydroxyl groups of the TCAC gives a new oxonium ion.
  6. Loss of water from this oxonium ion gives the ester and water

This article is in need of attention. ... Water (from the Anglo-Saxon and Low German wæter) is a colourless, tasteless, and odourless substance that is essential to all known forms of life and is the most universal solvent. ...

Examples

Benzocaine, a. ...

  Results from FactBites:
 
Hermann Emil Fischer at AllExperts (291 words)
Hermann Emil Fischer (October 9, 1852 - July 15, 1919) was a German chemist and recipient of the Nobel Prize for Chemistry in 1902.
Fischer was born in Euskirchen, near Cologne, the son of a businessman.
Fischer then attended the University of Bonn in 1872, but switched to the University of Strasbourg in 1872.
Hermann Emil Fischer Summary (4302 words)
Fischer's first step in unraveling the mysteries of the sugar group was the discovery in 1875 of phenyl hydrazine, a compound which could be used as a general reagent for separating and isolating sugars.
Fischer was elected to membership in the Academy of Sciences, and, in 1902, he received the Nobel Prize "for his synthesis in the groups of sugars and purine," as quoted by Eduard Farber in Nobel Prize Winners in Chemistry.
Fischer was dedicated to academic research and was among the first scientists in the world to promote substantial industrial as well as governmental support for university laboratories.
  More results at FactBites »


 

COMMENTARY     


Share your thoughts, questions and commentary here
Your name
Your comments
Please enter the 5-letter protection code

Want to know more?
Search encyclopedia, statistics and forums:

 


Lesson Plans | Student Area | Student FAQ | Reviews | Press Releases |  Feeds | Contact
The Wikipedia article included on this page is licensed under the GFDL.
Images may be subject to relevant owners' copyright.
All other elements are (c) copyright NationMaster.com 2003-5. All Rights Reserved.
Usage implies agreement with terms.