Acyl chlorides: Difference between revisions
Jump to navigation
Jump to search
Added the references correctly, that is, I added them as explained in the lecture. |
m Added link to acid page. |
||
| Line 1: | Line 1: | ||
In organic chemistry, an acyl chloride is a [[ | In organic chemistry, an acyl chloride is a [[Molecule|molecule]] with the functional group -COCl. Acyl chlorides are described as [[Acid|acid ]]derivitives, that is, -Cl is in place of -OH that would be seen in [[Carboxylic acid|carboxylic acid]] [[Compound|compounds]]. They do not dissolve in [[Water|water]] because they react with it via a [[Nucleophilic-addition-elimination|nucleophillic-addition-elimination]] reaction to give its acid derivative and [[HCl|HCl]]<ref>© Jim Clark 2004 (modified December 2015) https://www.chemguide.co.uk/organicprops/acylchlorides/background.html Date accessed:05/12/17</ref>. | ||
=== References === | === References === | ||
<references /> | <references /> | ||
Revision as of 14:01, 16 November 2018
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].
References
- ↑ © Jim Clark 2004 (modified December 2015) https://www.chemguide.co.uk/organicprops/acylchlorides/background.html Date accessed:05/12/17