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CBSE · Class 11 · Chemistry

Hydrocarbons quiz

Q01
MCQ

The general formula of alkynes is:

(a) CnH2n+2
(b) CnH2n
(c) CnH2n-2
(d) CnHn (1 mark)
Q02
MCQ

The more stable conformation of ethane is:

(a) eclipsed
(b) staggered
(c) skew
(d) both are equally stable (1 mark)
Q03
MCQ

Bromine water is decolourised by:

(a) ethane
(b) ethene
(c) methane
(d) benzene (1 mark)
Q04
MCQ

Addition of HBr to propene in the presence of peroxide gives:

(a) 2-bromopropane
(b) 1-bromopropane
(c) 1,2-dibromopropane
(d) propane (1 mark)
Q05
MCQ

Ethyne is prepared in the laboratory from:

(a) calcium carbonate
(b) calcium carbide
(c) ethanol
(d) methane (1 mark)
Q06
MCQ

Which of these is aromatic?

(a) Cyclohexane
(b) Benzene
(c) Cyclohexene
(d) Hexane (1 mark)
Q07
MCQ

The electrophile in nitration of benzene is:

(a) NO2-
(b) NO2+
(c) NO3-
(d) HNO3 (1 mark)
Q08
MCQ

Which group is meta-directing?

(a) -OH
(b) -CH3
(c) -NO2
(d) -NH2 (1 mark)
Q09
MCQ

Baeyer's reagent is:

(a) alkaline cold dilute KMnO4
(b) acidified K2Cr2O7
(c) bromine water
(d) Lindlar's catalyst (1 mark)
Q10
MCQ

Partial reduction of an alkyne with Lindlar's catalyst gives:

(a) trans-alkene
(b) cis-alkene
(c) alkane
(d) alcohol (1 mark)
Q11
Short

Why do alkanes undergo substitution while alkenes undergo addition reactions? (2 marks)

Q12
Short

What is aromatisation? Give an example. (2 marks)

Q13
Short

Why is benzene extraordinarily stable despite having three double bonds? (2 marks)

Q14
Short

What is Friedel-Crafts alkylation? Give an equation. (2 marks)

Q15
Short

How is propene prepared from 2-bromopropane? (2 marks)

Q16
Short

What is ozonolysis? What is its use? (2 marks)

Q17
Short

Why does cis-but-2-ene have a higher boiling point than trans-but-2-ene? (2 marks)

Q18
Short

Write the reaction for the cyclic polymerisation of ethyne. (2 marks)

Q19
Short

What is pyrolysis? Give an example. (2 marks)

Q20
Short

Why are some polynuclear hydrocarbons dangerous? (2 marks)

Q21
Numerical

Calculate the mass of carbon dioxide formed by complete combustion of 32 g of methane (C = 12, O = 16, H = 1). (3 marks)

Q22
Numerical

Calculate the number of sigma and pi bonds in benzene. (3 marks)

Q23
Numerical

How many structural isomers are possible for C5H12? Name them. (3 marks)

Q24
Numerical

Calculate the percentage of carbon in benzene (C = 12, H = 1). (3 marks)

Q25
Numerical

What volume of hydrogen at STP is needed to convert 5.2 g of ethyne completely into ethane (22.4 L/mol)? (3 marks)

Q26
Case

Read the passage and answer the questions. Propene reacts with HBr. In the absence of peroxide, the major product is 2-bromopropane. In the presence of benzoyl peroxide, the major product is 1-bromopropane. Kharasch explained this using a free radical mechanism. (i) Name the rule followed in the first case. (ii) What is the intermediate formed in the first case? (iii) Why does HCl not show the peroxide effect? (5 marks)

Q27
Case

Read the passage and answer the questions. Benzene undergoes electrophilic substitution reactions. In nitration, a mixture of concentrated nitric acid and concentrated sulphuric acid is used. The reaction proceeds by the formation of an electrophile, followed by a carbocation intermediate, and then the loss of a proton. (i) Write the equation for the formation of the electrophile. (ii) What is the intermediate called? (iii) Why does benzene undergo substitution rather than addition? (5 marks)

Q28
Case

Read the passage and answer the questions. Alkanes are used as fuels. Methane is the main component of CNG, while LPG contains mainly butane and propane. When alkanes burn in sufficient air, they release a large amount of heat. In insufficient air, carbon monoxide and soot are formed. (i) Write the equation for the combustion of butane. (ii) Why is incomplete combustion dangerous? (iii) Why is methane a cleaner fuel than coal? (5 marks)

Q29
Case

Read the passage and answer the questions. Alkenes show geometrical isomerism due to restricted rotation around the carbon-carbon double bond. For example, but-2-ene exists as cis and trans isomers. The cis isomer has a dipole moment, while the trans isomer has almost zero dipole moment. (i) Why is rotation restricted? (ii) Why does the trans isomer have nearly zero dipole moment? (iii) Can but-1-ene show geometrical isomerism? Explain. (5 marks)

Q30
Case

Read the passage and answer the questions. Ethyne can be converted into benzene by passing it through a red-hot iron tube at 873 K. Benzene can also be prepared by decarboxylation of sodium benzoate with soda lime, or by reducing phenol with zinc dust. (i) Write the equation for decarboxylation of sodium benzoate. (ii) Name the reaction converting ethyne to benzene. (iii) Write the equation for the reduction of phenol. (5 marks)

Q31
Long/Diagram

Describe the methods of preparation of alkanes and their chemical properties with equations. (6 marks)

Q32
Long/Diagram

Explain the conformations of ethane with Newman and sawhorse projections. Why is the staggered form more stable? (6 marks)

Q33
Long/Diagram

Describe the preparation and chemical properties of alkenes, including Markovnikov's rule and the peroxide effect. (6 marks)

Q34
Long/Diagram

Describe the preparation of ethyne. Explain its acidic character and addition reactions. (6 marks)

Q35
Long/Diagram

Explain the structure and aromaticity of benzene. Describe its electrophilic substitution reactions with mechanism and the directive influence of substituents. (6 marks)

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