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.
Why is chlorobenzene resistant to nucleophilic substitution reactions?
(a) Define the following:
(i) Enantiomers
(ii) Racemic mixture
Write the structures of A, B, and C in the following sequence of reactions:
(A) Explain the following reactions and write chemical equations involved:
(a) Wolff-Kishner reduction
(b) Etard reaction
(c) Cannizzaro reaction
Write IUPAC names of the following coordination entities:
(a) \( [Fe(en)_2Cl_2]^+ \)
(b) \( [Co(NH_3)_4(H_2O)Br]SO_4 \)
(c) \( [Ni(CN)_4]^{2-} \)