Acetyl chloride: Difference between revisions
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File:Acetyl-chloride-3D-vdW.png|3D van der Waals model of Acetyl chloride | |||
File:Acetyl_chloride_25ml.jpg|25 ml bottle of Acetyl chloride | |||
File:Pili_Nut_(Sipocot,_Camarines_Sur).jpg|Pili Nut from Sipocot, Camarines Sur | |||
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Latest revision as of 00:44, 18 February 2025
Acetyl chloride[edit]


Acetyl chloride is an organic compound with the formula CH3COCl. It is a colorless, corrosive, volatile liquid. Acetyl chloride is a member of the acyl chloride family and is used as an important reagent in organic synthesis.
Structure and properties[edit]
Acetyl chloride consists of a carbonyl group (C=O) attached to a methyl group (CH3) and a chlorine atom. The molecule is planar, and the carbonyl carbon is sp2 hybridized. Acetyl chloride is highly reactive due to the presence of the electron-withdrawing chlorine atom, which makes the carbonyl carbon more electrophilic.
Preparation[edit]
Acetyl chloride can be prepared by the reaction of acetic acid with thionyl chloride (SOCl2):
- CH3COOH + SOCl2 _ CH3COCl + SO2 + HCl
This reaction is commonly used in laboratories to produce acetyl chloride.
Reactions[edit]
Acetyl chloride is a versatile reagent in organic chemistry. It is used to introduce the acetyl group into alcohols and amines to form esters and amides, respectively. For example:
- Reaction with alcohols:
- ROH + CH3COCl _ CH3COOR + HCl
- Reaction with amines:
- RNH2 + CH3COCl _ CH3CONHR + HCl
Acetyl chloride also reacts with water to form acetic acid and hydrochloric acid:
- CH3COCl + H2O _ CH3COOH + HCl
Safety[edit]
Acetyl chloride is a corrosive and lachrymatory liquid. It should be handled with care, using appropriate personal protective equipment such as gloves and goggles. It reacts violently with water and should be stored in a dry environment.
Related pages[edit]
-
3D van der Waals model of Acetyl chloride
-
25 ml bottle of Acetyl chloride
-
Pili Nut from Sipocot, Camarines Sur