To solve this problem, we need to compare the acidity of phenol (C6H5OH), alcohol (ROH), and water (H2O).
1. Understanding Acid Strength:
Acid strength depends on the ability of the molecule to donate a proton (H+). This is determined by the stability of the conjugate base formed after proton loss.
2. Phenol (C6H5OH) vs Alcohol (ROH):
Phenol is more acidic than alcohol because the negative charge on the oxygen in the phenoxide ion (C6H5O-) is stabilized by resonance with the aromatic ring. In contrast, the negative charge on the oxygen in the alkoxide ion (RO-) is not stabilized, making alcohol less acidic than phenol.
3. Phenol (C6H5OH) vs Water (H2O):
Water (H2O) is a weaker acid than phenol. Although water can donate a proton to form the hydroxide ion (OH-), the conjugate base of phenol is more stable due to resonance stabilization.
4. Conclusion:
The correct order of acid strength is: Water > Phenol > Alcohol.
Final Answer:
The correct option is (D) H2O > C6H5OH > ROH.
Write IUPAC names of the following compounds and classify them into primary, secondary and tertiary amines.
(i) (CH3 )2CHNH2 (ii) CH3 (CH2 )2NH2 (iii) CH3NHCH(CH3 )2
(iv) (CH3 )3CNH2 (v) C6H5NHCH3 (vi) (CH3CH2 )2NCH3 (vii) m–BrC6H4NH2
Give one chemical test to distinguish between the following pairs of compounds.
(i) Methylamine and dimethylamine
(ii) Secondary and tertiary amines
(iii) Ethylamine and aniline
(iv) Aniline and benzylamine
(v) Aniline and N-methylaniline
Account for the following:
(i) pKb of aniline is more than that of methylamine.
(ii) Ethylamine is soluble in water whereas aniline is not.
(iii) Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.
(iv) Although amino group is o– and p– directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.
(v) Aniline does not undergo Friedel-Crafts reaction.
(vi) Diazonium salts of aromatic amines are more stable than those of aliphatic amines. (vii) Gabriel phthalimide synthesis is preferred for synthesising primary amines.