Physical Properties of Alcohols and Phenols
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- Phenoxide ion is better stabilized by resonance than acetate ion.
- Acetate ion is better stabilized by resonance than phenoxide ion.
- Phenol is less solute in water than acetic acid.
- Both phenoxide ion and acetate ion are stable.
Why Ethanol is soluble in water?
1.Intramolecular hydrogen bonding present in ortho-nitrophenol
2.Intermolecular hydrogen bonding present in para-nitrophenol
3.Intramolecular hydrogen bonding present in para-nitrophenol
4.Inter-molecular hydrogen bonding present in ortho-nitrophenol.
- 1&3
- 1&2
- 2 only
- 1, 3 &4
Out of o - nitrophenol and p - nitrophenol, which is more volatile? Explain.
[1 mark]
- butan-2-ol
- butan-1-ol
- 2-methylpropan-1-ol
- 2-methylpropan-2-ol
The halides in which the halogen atom is bonded to an sp2 hybridised carbon of a carbon-carbon double bond are:
Vinylic halides
Allylic halides
Benzyllic halides
Aryl halides
Why alcohol and glucose do not conduct electricity? Explain in detail.
which has higest aromatic character
1. pyrol
2. furane
3. thiophene
The dipole moment of phenol is smaller than that of methanol. Why?
Explain why propanol has a higher boiling point than that butane?
Why is the carbon in carbonium ion sp2 hybridised?
Does phenol react with ?
Why basicity of and are and respectively?
Why is order of boiling point of alcohols is 3°>2°>1° ?
Why is acetone soluble in oil and water?
Assertion (A) Boiling points of alcohols and ethers are high.
Reason (R) They can form intermolecular hydrogen-bonding.
(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.
The decreasing order of boiling points of the following alcohols
The carbon-oxygen bond in phenol is slightly stronger than that in methanol. Why ?
In which one of the following keto-enol system is the keto form more stable than the enol form?
CH3−CH2−O||C−CH3⇌ CH3−CH2−OH|C=CH2
Arrange the following compounds in increasing order of boiling point. Propan - 1 - ol, butan - 1 - ol, butan - 2 - ol, pentan - 1 - ol
(a) Propan-1-ol, butan-2-ol, butan - 1 - ol, pentan-1-o|
(b) Propan-1-ol, butan - 1 - ol, butan-2-ol, pentan-1-ol
(c) Propan-1-ol, butan-2-ol, butan-1-ol, pentan-1-ol
(d) Propan-1-ol, butan-1-ol, butan-2-ol, pentan-1-ol
- Glycerine
- Glycerol
- Propane−1, 2, 3−triol
- Ethanol
(a) H3C−OH|C|OH3−H (b)Br3C−OH|C|OH−H
(c) F3C−OH|C|OH−H (d)H5C6−OH|C|OH−C6H5
- a
- c
- d
- b
- Have same solubility in water
- Have same boiling point
- Have same refractive indices
- Have same magnitude of angle of rotation of plane polarised light and direction