Williamson synthesis is the best method for the preparation of ethers.
Alcohols, Phenols and Ethers
Phenols react with alkyl halides in alkaline medium to form ethers. Therefore,
Acid reacts with sodium hydrogen carbonate as follows : Among all the given options ortho-nitrophenol is weaker acid than HCO 3 hence, it does not react with NaHCO 3 .
The iodoform test is positive for alcohols with formula R — CHOH — CH 3 .
Among C 6 H 14 O isomers, the ones with positive iodoform test are:
Glycol is used as an antifreeze in automobiles.
Glycerol when treated with excess HI produces 2–iodopropane.
The iodoform test is exhibited by ethyl alcohol, acetaldehyde, acetone, methyl ketones, those alcohols which possess CH 3 CH(OH)— group, acetophenone, -hydroxypropionic acid, keto acid, 2-aminoalkanes, etc.
In phenols, the presence of electron releasing groups decrease the acidity, whereas presence of electron withdrawing groups increase the acidity, compared to phenol.
Among the meta and para-nitrophenols, the latter is more acidic as the presence of –NO 2 group at para position stabilises the phenoxide ion to a greater extent than when it is present at meta position.
Thus, correct order of acidity is : (iv) > (iii) > (i) > (ii)
As we know that phenols and carboxylic acids are more acidic than aliphatic alcohols thus cyclohexanol is least acidic.
On the other hand III is more acidic than IV because of the presence of three highly electron with drawing NO 2 groups on the benzene ring which makes the OH bond extremely polarized.
This facilitates the release of H + .
In acetic acid the electron withdrawing
group polarizes the O-H bond and increases the acid strength.
Thus, acetic acid is more acidic than phenol or cyclohexanol.
Thus, the order of acidic strength will be III > II > IV > I
All alcohols follow the general formula as C n H 2n+2 O.