Acidity of Alcohols and Phenols
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In the following compounds,
The order of acidity is
III > IV > I > II
I > IV > III > II
II > I > II > IV
IV > III > I > II
Statement I:
The acidic strength of monosubstituted nitrophenol is higher than phenol because of electron withdrawing nitro group.
Statement II:
o−nitrophenol, m−nitrophenol and p−nitrophenol will have same acidic strength as they have one nitro group attached to the phenolic ring.
In the light of the above statements, choose the most appropriate answer from the options given below:
- Statement I is incorrect but Statement II is correct
- Both statement I and Statement II are correct
- Statement I is correct but Statement II is incorrect
- Both Statement I and Statement II are incorrect
Which of the following is most acidic?
(a) Benzyl alcohol
(b) Cyclohexanol
(c) Phenol
(d) m - chlorophenol
Give two reactions that show the acidic nature of phenol. Compare acidity of phenol with that of ethanol.
- C6H6>C6H5−OH>C6H5−Cl>C6H5−COOH
- C6H5−OH>C6H6>C6H5−Cl>C6H5−COOH
- C6H5−Cl>C6H6>C6H5−OH>C6H5−COOH
- C6H5−OH>C6H6>C6H5−COOH>C6H5−Cl
Explain why p-nitrophenol is more acidic than phenol?
Phenol is less acidic than . . . .
(a) ethanol
(b) o - nitrophenol
(c) o-methylphenol
(d) o - methoxyphenol
- Ethanol
- 2 – propanol
- 2 – Methyl – 2 – butanol
- Na metal
Why is the enthalpy of neutralization of weak acid less than that of a strong acid
Complete the following reaction:
The order of reactivity of following alcohols with halogen acids is .......
(A) CH3CH2−CH2−OH (B)
(a) (A) > (B) > (C) (b) (C) > (B) > (A)
(c) (B) > (A) > (C) (d) (A) > (C) > (B)
- C2H5OH
- CH3CONH2
- CH(CN)3
Arrange water, ethanol and phenol in increasing order of acidity and give reason for your answer.
Explain why is ortho nitrophenol more acidic than ortho methoxyphenol?
Which of the following will maximum pKa value?
- o-nitrophenol
- Phenol
- o-cresol
- ethanol
- nucleophilic substitution
- nucleophilic addition
- electrophilic substitution
- free radical substitution
The ionisation constant of phenol is higher than that of ethanol because
Phenoxide ion is bulkier than ethoxide
Phenoxide ion is stronger base than ethoxide
Phenoxide ion is stabilised through delocalisation
Phenoxide ion is less stable than ethoxide
Assertion (A) Ethanol is a weaker acid than phenol.
Reason (R) Sodium ethoxide may be prepared by the reaction of ethanol with aqueous NaOH.
(a) Assertion and reason both are correct and reason is correct explanation of assertion.
(b) Assertion and reason both are wrong statements.
(c) Assertion is correct statement but reason is wrong statement.
(d) Assertion is wrong statement but reason is correct statement.
(e) Both assertion and reason are correct statements but reason is not correct explanation of assertion.
Out of o-nitrophenol and o-cresol which is more acidic?
Compound 'X' also gives violet colour with neutral FeCl3 solution. The compound 'X' is :
Which of the following compounds will react with sodium hydroxide solution in water?
(a) C6H5OH
(b) C6H5CH2OH
(c) (CH3)3COH
(d) C2H5OH
Choose the correct word from the bracket and fill in the blanks.
Commercial alcohol is made unfit for drinking by the addition of _________(methanol/ethanol).
- CH3COCH3
- CH3CH2CH2COOH
- CH3CH=CH2
- CH3CHO
Which of the following is soluble in water?
- Both (b) and (c)
Write the reactions of (i) aromatic and (ii) aliphatic primary amines with nitrous acid.