The two-part name of an ester: the name of the hyrocarbon group from the alcohol comes first, then the name of the carboxylate group derived from the acid name by replacing "-ic" with "-ate"
Therefore the name will be ethyl salicylate C9H10O4 (Google it to get the image)
Salicylic acid: A benzene ring having a carboxilic group (COOH) and a hyrdoxide group (OH) at ortho positions to each other
Ethanol: CH3-CH2-OH or OH-CH2-CH3
When combining ethanol and salicylic acid it will react and create a ethyl salicylate. Ethyl salicylate is the ester formed with the combination of ethyl and salicylic acid.
C6h4(oh)(cooh)
acetylsalicylic acid
acetic anhydride and sodium chloride will form.
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.
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.
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Synthesis of acetyl chloride via the reaction of acetic acid with sulphuric acid
yes
acetic anhydride and sodium chloride will form.
Acetyl salicylic acid.
Acetyl salicylic acid (asperinR), Ammonium chloride (sal volatile), Penicillinic acid and Clavulanic acid (both antbiotics)
acetyl salicylic acid?
4-acetyl biphenyl
Aspirin is acetyl salicylic acid.
This compound is acetyl salicylic acid or aspirin.
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.
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.