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
i do not have the answer
The nucleophilic nitrogen attacks the carbonyl carbon of acetyl chloride. HCl gas is released and acetyl glycine is formed.
Because Salicylic Acid reacts with Acetic Anhydride in the presence of H2SO4 and CH3COOH to give Aspirin. The sulphuric acid does not react. If you measure the volume/weight of the acid before the reaction and after the reaction, there will be no change. Note:-You can also use Acetyl Chloride in the presence of phosphoric acid instead on Acetic Anhydride.
Actually it is possible to put a second acyl group on as well, for example with acetyl chloride and triethylamine. Under aqueous basic conditions the second acyl group is far more readily hydrolysed.
The mechanism for absorption is improved in the hydrochloride version, but I could be mistaken.
acetic anhydride and sodium chloride will form.
i do not have the answer
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.
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.
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
hydrogen ions
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?