acetic anhydride and sodium chloride will form.
these two are soluble, but there is no chemical reaction between them
The name of this reaction is Friedel-Crafts acylation. It should have a major product adding a ketone at the para position with regard to the isopropyl of the cumene.
Ten nonbonding electrons and 14 bonding electrons are in acetyl chloride.
Around .16
This is an example of a Friedel-Crafts acylation. One hydrogen from the benzene is replaced by the acetyl portion of the acetyl chloride and the hydrogen and chloride from the benzene and acetyl chloride respectively combine to form HCl. Please see the link.
The chemistry of acetyl chloride is not as a methyl ketone but as an acyl halide. All the action is on the carbon atom with the oxygen and chlorine. In the haloform reax the methyl carbon gets attacked losing a proton, picking up a halide and leaving an OH behind to form an acid and a haloform.
i do not have the answer
Synthesis of acetyl chloride via the reaction of acetic acid with sulphuric acid
4-acetyl biphenyl
The name of this reaction is Friedel-Crafts acylation. It should have a major product adding a ketone at the para position with regard to the isopropyl of the cumene.
Ten nonbonding electrons and 14 bonding electrons are in acetyl chloride.
Around .16
This was asked in a coursework paper to my sister and she could not find an answer ..so far neither can I...I did find where it gave off hydrogen in a reaction..not sure on t6his hehe it may be CH3-CO-Cl + H2 = CH3-CO-H + HCl
This is an example of a Friedel-Crafts acylation. One hydrogen from the benzene is replaced by the acetyl portion of the acetyl chloride and the hydrogen and chloride from the benzene and acetyl chloride respectively combine to form HCl. Please see the link.
The nucleophilic nitrogen attacks the carbonyl carbon of acetyl chloride. HCl gas is released and acetyl glycine is formed.
A Condensation reaction between oxaloacetate and acetyl CoA by the enzyme citrate synthase
The chemistry of acetyl chloride is not as a methyl ketone but as an acyl halide. All the action is on the carbon atom with the oxygen and chlorine. In the haloform reax the methyl carbon gets attacked losing a proton, picking up a halide and leaving an OH behind to form an acid and a haloform.
The benzyl group acts as a protector retarding hydrolysis?