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ALc PH Eth MCQ

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Class 12 Alcohols, Phenols, and Ethers MCQs

1. To get carboxylic acids directly from alcohol, which of the


following oxidising agents is used?
a) Alkaline KMnO4
b) Aqueous KMnO4
c) Acidified KMnO4
d) Anhydrous CrO3
Answer: c
Explanation: Strong oxidizers, such as acidified potassium
permanganate or acidified potassium dichromate, convert
alcohol to carboxylic acid immediately. Using CrO3 as the
oxidising agent in an anhydrous media, however, only aldehyde
can be produced.
2. When phenol reacts with bromine water, what is the result?
a) Brown liquid
b) Colourless gas
c) White precipitate
d) No reaction
Answer: c
Explanation: When phenol is treated with bromine water, a
white precipitate is formed, which is 2,4,6-Tribromophenol.
3. The Lucas test was carried out on three different
compounds: A, B, and C. Compounds A and B were turbid at
ambient temperature, while compound C did not become turbid
until it was heated. Which one of the compounds is tertiary in
structure?
a) A
b) Cannot be determined
c) C
d) A and B
Answer: b
Explanation: It is stated that A and B exhibit turbidity at room
temperature, however, it is not stated whether the turbidity
appears immediately or over a period of time. So compounds A
and B may be tertiary or secondary depending on whether
turbidity appears immediately or after 5 minutes respectively.
Compound C may be primary.
4. Which of the following compounds is formed when
secondary alcohols are oxidised by [O]?
a) Ether
b) Aldehyde
c) Ketone
d) Amine
Answer: c
Explanation: The oxidation of secondary alcohols by a nascent
oxygen atom [O] yields the ketone molecule.
5. Which of the following processes does not result in the
production of alcohol?
a) Acid catalysed hydration of alkenes
b) Free radical halogenation of alkanes
c) Reduction of aldehydes
d) Hydroboration-oxidation of alkenes
Answer: b
Explanation: When alkanes are halogenated by free radicals,
they form a mixture of haloalkanes rather than alcohols.
Alcohols can be made from alkenes through acid catalysed
hydration, and hydroboration-oxidation, and from aldehyde
reduction.
6. The conversion of trialkyl borane to an alcohol does not
require which of the following?
a) Sodium hydroxide
b) Water
c) Diborane
d) Hydrogen peroxide
Answer: c
Explanation: In the presence of aqueous NaOH, trialkyl
boranes are oxidised by hydrogen peroxide to produce alcohol.
This conversion does not require diborane, although it is
required for the creation of trialkyl boranes.
7. Ethers may be used as solvents because they react only with
which of the following reactants?
a) Oxidising agent
b) Bases
c) Acids
d) Reducing agents
Answer: c
Explanation: Nucleophiles and bases cannot attack ether.
However, because of their capacity to solve cations by giving
an electron pair from an oxygen atom, they are excellent
solvents in many chemical reactions. Ethers are less reactive
than alcohols and react only with acids.

8. An aryl carbon can be found in which of the following


compounds?
a) Ethanol
b) Phenol
c) Vinyl alcohol
d) Benzyl alcohol
Answer: b

Explanation: An aryl carbon is the sp2 hybridised carbon of an


aromatic ring to which the hydroxyl group is connected. The OH
group is connected to an aryl carbon in phenol.
9. It’s called ether when the alkyl groups connected to either
side of the oxygen atom in an ether are different.
a) mixed
b) symmetrical
c) simple
d) diethyl
Answer: a
Explanation: A mixed or unsymmetrical ether is one in which
the alkyl or aryl groups on either side of the O atom differ.
10. Which of the following alcohols is not polyhydric?
a) Propylene glycol
b) Ethylene glycol
c) Cyclohexanol
d) Benzene-1,2-diol
Answer: c
Explanation: Polyhydric alcohols include two or more hydroxyl
groups and are classified as glycols in the common system or
diols and triols in the IUPAC system.

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