Alcohols, Phenols and Ethers
Each subtopic includes About section, revision page link, 10 preview questions, and practice CTAs.
Nomenclature and methods of preparation
SubtopicNomenclature and methods of preparation under Alcohols, Phenols and Ethers for Grade 12 ICSE.
Preview questions (no answers)
- 1.
Which of the following reagents is most suitable for the reduction of a carboxylic acid to a primary alcohol?
A.B.C.(Pyridinium chlorochromate)
D. - 2.
What is the IUPAC name for the simplest hydroxy derivative of benzene, commonly known as Phenol?
A.Cyclohexanol
B.Hydroxybenzene
C.Benzenol
D.Phenyl alcohol
- 3.
The acid-catalyzed hydration of ethene () produces which of the following alcohols?
A.Methanol
B.Ethanol
C.Propan-1-ol
D.Ethane-1,2-diol
Download the worksheet for Alcohols, Phenols and Ethers - Nomenclature and methods of preparation to practice offline. It includes additional chapter-level practice questions.
Physical and chemical properties
SubtopicPhysical and chemical properties under Alcohols, Phenols and Ethers for Grade 12 ICSE.
Preview questions (no answers)
- 1.
When phenol is treated with excess bromine water, the product obtained is:
A.o-Bromophenol
B.p-Bromophenol
C.2,4,6-Tribromophenol
D.m-Bromophenol
- 2.
An unknown alcohol was treated with Lucas reagent ( + conc. ). The observations are summarized in the flowchart below. Based on the diagram, identify the type of alcohol that reacts immediately.
A.Primary alcohol
B.Secondary alcohol
C.Tertiary alcohol
D.Dihydric alcohol
- 3.
The solubility of lower alcohols in water is primarily due to:
A.The formation of hydrogen bonds with water molecules
B.The covalent nature of the bond
C.The hydrophobic nature of the alkyl group
D.The high boiling point of alcohols
Download the worksheet for Alcohols, Phenols and Ethers - Physical and chemical properties to practice offline. It includes additional chapter-level practice questions.
Primary, secondary and tertiary alcohols
SubtopicPrimary, secondary and tertiary alcohols under Alcohols, Phenols and Ethers for Grade 12 ICSE.
Preview questions (no answers)
- 1.
The vapors of a primary alcohol are passed over heated copper at . The main organic product formed is:
A.A ketone
B.An alkene
C.A carboxylic acid
D.An aldehyde
- 2.
In the Victor Meyer's test, a primary alcohol produces a characteristic color. What is this color?
A.Blue
B.Blood Red
C.Colorless
D.Green
- 3.
When a tertiary alcohol is treated with Lucas reagent (conc. and anhydrous ) at room temperature, the turbidity appears:
A.Immediately
B.After 5 to 10 minutes
C.Only upon heating
D.Turbidity is not formed at all
Download the worksheet for Alcohols, Phenols and Ethers - Primary, secondary and tertiary alcohols to practice offline. It includes additional chapter-level practice questions.
Mechanism of dehydration
SubtopicMechanism of dehydration under Alcohols, Phenols and Ethers for Grade 12 ICSE.
Preview questions (no answers)
- 1.
What small molecule is eliminated as a byproduct during the conversion of to ?
A.B.C.D. - 2.
In the mechanism of dehydration of ethanol to ethene, what is the first step?
A.Formation of a carbocation
B.Protonation of the alcohol to form an oxonium ion
C.Loss of a proton from the beta-carbon
D.Nucleophilic attack of on the alcohol
- 3.
The correct order of reactivity of alcohols towards acid-catalyzed dehydration is:
A.B.C.D.
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Acidic nature of phenol
SubtopicAcidic nature of phenol under Alcohols, Phenols and Ethers for Grade 12 ICSE.
Preview questions (no answers)
- 1.
In the phenoxide ion, the negative charge is delocalized over the ortho and para positions of the benzene ring. This makes the phenoxide ion:
A.Less stable than the neutral phenol molecule
B.More stable than the neutral phenol molecule
C.Equally stable as the ethoxide ion
D.Highly reactive towards electrophilic substitution only
- 2.
The presence of an electron-withdrawing group (EWG) like on the benzene ring of phenol:
A.Decreases the acidity by destabilizing the phenoxide ion
B.Has no effect on the acidic strength
C.Increases the acidity by stabilizing the phenoxide ion
D.Increases the value of the phenol
- 3.
Which of the following reagents can react with phenol to demonstrate its acidic nature by forming a salt?
A.B.C.D.
Download the worksheet for Alcohols, Phenols and Ethers - Acidic nature of phenol to practice offline. It includes additional chapter-level practice questions.
Electrophilic substitution in phenols
SubtopicElectrophilic substitution in phenols under Alcohols, Phenols and Ethers for Grade 12 ICSE.
Preview questions (no answers)
- 1.
Identify the major product obtained when phenol is treated with dilute at low temperature ():
A.m-Nitrophenol
B.A mixture of o-nitrophenol and p-nitrophenol
C.Picric acid
D.Nitrobenzene
- 2.
Picric acid is chemically known as:
A.2,4,6-Trinitrophenol
B.2,4-Dinitrophenol
C.o-Nitrophenol
D.Trinitrotoluene
- 3.
The group in phenol is:
A.Deactivating and meta-directing
B.Activating and ortho, para-directing
C.Activating and meta-directing
D.Deactivating and ortho, para-directing
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Preparation and properties of ethers
SubtopicPreparation and properties of ethers under Alcohols, Phenols and Ethers for Grade 12 ICSE.
Preview questions (no answers)
- 1.
In the dehydration of ethanol using concentrated , identify 'Compound X' based on the temperature conditions shown in the diagram.
A.Ethene
B.Ethane
C.Ethoxyethane
D.Ethyl hydrogen sulfate
- 2.
Ethers are soluble in water to a certain extent, similar to alcohols of comparable molecular mass. This solubility is attributed to:
A.The formation of ionic bonds with water
B.The ability of ether oxygen to form hydrogen bonds with water molecules
C.The presence of high London dispersion forces
D.The low density of ethers compared to water
- 3.
Which of the following reaction conditions is used in the Williamson synthesis of diethyl ether?
A.Ethanol and concentrated at
B.Ethyl bromide and sodium ethoxide
C.Ethanol and phosphorus pentachloride
D.Ethyl bromide and aqueous
Download the worksheet for Alcohols, Phenols and Ethers - Preparation and properties of ethers to practice offline. It includes additional chapter-level practice questions.