Phenoxide ion is C6H5O-, formed when phenol, C6H5OH is treated with a base like NaOH.
yes
When the reaction of sodium phenoxide and sulforic acid occurs, the esters are usually produced.
An aryloxide is an alternative name for a phenoxide, any metallic salt of a phenol.
The ion produced is phenoxide ion.
The reaction is:Na2S + 2 HCl = 2 NaCl + H2S
Carboxylic acid.
yes
When the reaction of sodium phenoxide and sulforic acid occurs, the esters are usually produced.
In the phenoxide ion the charge is delocalized by the resonance in the benzene ring. There is no such delocalization in the ethoxide ion.
The ion produced is phenoxide ion.
An aryloxide is an alternative name for a phenoxide, any metallic salt of a phenol.
To prepare the phenoxide, dissolve 23.5 grams of Csl-IsOl-I in 875 milliliters of toluene. On a separate dish, dissolve 10 grams of NaOH in 150 milliliters of methyl alcohol. Pour the solution into a flask and mix.
The reaction is:Na2S + 2 HCl = 2 NaCl + H2S
Because in sodium hydroxide it forms phenoxide ion which is stabilized by solvolysis.
Aspirin (acetyl salycilic acid) is prepared from salycilic acid and acetic anhydride; salicylic acid is prepared from sodium phenoxide and carbon dioxide (Kolbe synthesis).
Phenoxide and Hydrochloric acid: C6H5O-Na+ + HCL ----> C6H5OH + NaCl
Electron density on oxygen in phenoxide ion is decreased due to resonance. The oxygen rather acquire a positive charge. Therefore phenol does not give protonation readily