Acetanilide
The formation of aspirin will proceed faster if acetic anhydride is used in place of acetic acid. However, acetic anhydride will hydrolyze in the presence of water to form acetic acid, slowing down the reaction.
Dehydration of acetic acid to prepare acetic anhydride occur at 8oo oC.
copper acetate monohydrate and glacial acetic acid
Salycylic acid and acetic anhydride with a sulphuric acid catalyst
They are miscible.
If the excess acetic anhydride is not removed in the reaction vessel an unwanted reaction will occur. The acetic anhydride will react causing esterification.
No it is not among these.
The formation of aspirin will proceed faster if acetic anhydride is used in place of acetic acid. However, acetic anhydride will hydrolyze in the presence of water to form acetic acid, slowing down the reaction.
The reaction is: (CH3CO)2O + H2O = 2 CH3COOH
Glacial acetic acid doesn't have water in it. Acetic acid ordinarily would be in a solution. Acetic acid is a weak acid, but it can be very concentrated. Glacial acetic acid is a acetic acid of a high purity more then 99.75 %
As an anhydride, It can be prepared by dehydrating its acid, i.e. Acetic acid, by strong dessicant such as Tetraphosphorus decaoxide(P4O10) :P4O10 + 12 CH3COOH ----> 4 H3PO4 + 6(CH3CO)2O
glaycil-analil
The chemical reaction is:C6H5NH2 + (CH3CO)2O → C6H5NHCOCH3 + CH3COOH
Yes it can be, but the reaction might be slower
(CH3CO)2O (s) + H2O (l) ----------> 2 CH3COOH (aq)
by urea hydrogen peroxide reaction with tri fluro acetic anhydride
An anhydride is not an acid and not a base.