General molecular formula of alkanols is C n H 2n+2 O or C n H 2n+1 OH
Alcohols, Phenols and Ethers
In case of unsymmetric ethers when treated with HI then I – attaches to smaller and less complex alkyl group as it follows S N 2 mechanism CH 3 O CH(CH 3 ) 2 + HI CH 3 I + (CH 3 ) 2 CHOH
Phenols are more acidic than alcohols as they are resonance stabilised whereas alcohols are not.
Further –NO 2 is an electron withdrawing group which increases acidic character and facilitates release of proton, whereas –CH 3 is an electron donating group which decreases acidic character, thus removal of H + becomes difficult.
Formation of a yellow precipitate on heating a compound with an alkaline solution of iodine is known as iodoform reaction.
Methyl alcohol does not respond to this test.
Iodoform test is exhibited by ethyl alcohol, acetaldehyde, acetone, methyl ketones and those alcohols which possess CH 3 CH(OH) – group.
n-propyl alcohol on oxidation with K 2 Cr 2 O 7 gives an aldehyde which on further oxidation gives an acid.
Isopropyl alcohol on oxidation gives a ketone with the same number of carbon atoms as original alcohol.
C 2 H 5 OH + 4I 2 + NaOH CHI 3 + NaI + HCOONa + H 2 O Iodoform is a pale yellow solid which crystallises in hexagonal plates.
Match with $$ value)
| List - I | List - II | ||
|---|---|---|---|
| (A) | Ethanol | (I) | 10.0 |
| (B) | Phenol | (II) | 15.9 |
| (C) | m-Nitrophenol | (III) | 7.1 |
| (D) | p-Nitrophenol | (IV) | 8.3 |
LiAlH4 reduces esters to alcohols but does not reduce C = C.
CH3CH = CHCH2OH + CH3OH
The dehydration of alcohol to form alkene occurs in following three step. Step
is initiation step.
Acidic strength Ethanol give lucas test after long time Statement (I) correct Statement (II) incorrect