Acyl chlorides: Difference between revisions

From The School of Biomedical Sciences Wiki
Jump to navigation Jump to search
Provided some information.
 
mNo edit summary
Line 1: Line 1:
&nbsp;In organic chemistry, an acyl chloride is a molecule with the functional group -COCl. Acyl chlorides are described as acid derivitives, that is, -Cl is in place of -OH that would be seen in carboxylic acid compounds. They do not dissolve in water because they react with it via a[[nucleophilic-addition-elimination|nucleophillic-addition-elimination]] reaction to give its acid derivative and HCl. <ref>© Jim Clark 2004 (modified December 2015) https://www.chemguide.co.uk/organicprops/acylchlorides/background.html Date accessed:05/12/17</ref>
&nbsp;In organic chemistry, an acyl chloride is a molecule with the functional group -COCl. Acyl chlorides are described as acid derivitives, that is, -Cl is in place of -OH that would be seen in carboxylic acid compounds. They do not dissolve in water because they react with it via a&nbsp;[[Nucleophilic-addition-elimination|nucleophillic-addition-elimination]] reaction to give its acid derivative and HCl. <ref>© Jim Clark 2004 (modified December 2015) https://www.chemguide.co.uk/organicprops/acylchlorides/background.html Date accessed:05/12/17</ref>

Revision as of 14:42, 5 December 2017

 In organic chemistry, an acyl chloride is a molecule with the functional group -COCl. Acyl chlorides are described as acid derivitives, that is, -Cl is in place of -OH that would be seen in carboxylic acid compounds. They do not dissolve in water because they react with it via a nucleophillic-addition-elimination reaction to give its acid derivative and HCl. [1]

  1. © Jim Clark 2004 (modified December 2015) https://www.chemguide.co.uk/organicprops/acylchlorides/background.html Date accessed:05/12/17