Hydrocarbons Test (16/02/02026)
Genius Science Academy
TEST PAPER: HYDROCARBONS
Time: 3 Hours | Marks: 100 | Date: 16/02/2026
SECTION A: ONE LINE QUESTIONS (25 Marks)
Answer all questions. (1 mark each)
- Define Hydrocarbons.
- What is the general formula for Alkanes?
- Why are alkanes called 'paraffins'?
- State the hybridization of carbon atoms in Alkenes.
- What is the C-C bond length in Alkanes?
- Define 'Isomerism'.
- What is the general formula for Alkynes?
- Define 'Conformations'.
- What is a 'Torsion angle'?
- Name the parent compound of the entire family of aromatic compounds.
- What is the common name for Alkenes?
- Give the IUPAC name of the first member of the Alkyne series.
- State Huckel’s Rule for aromaticity.
- Which alkane is the major product in a Wurtz reaction using a mixture of alkyl halides?
- What are 'Arenes'?
- Name the catalyst used for the hydrogenation of ethene at room temperature.
- Define 'Vicinal Dihalides'.
- What is the geometry of a benzene molecule?
- Name one ortho-para directing group.
- Mention one meta-directing group.
- What is the torsion angle in an 'eclipsed' conformation of ethane?
- Which gas is produced during the complete combustion of alkanes?
- Give the chemical formula for 'Sodium Ethynide'.
- Define 'Torsional Energy'.
- Name a known carcinogenic aromatic hydrocarbon.
SECTION B: ANSWER IN SHORT (20 Marks)
Answer any 10 out of 12 questions. (2 marks each)
- Differentiate between 'Cis' and 'Trans' isomers in alkenes.
- Explain the 'Saytzeff's Rule' with an example.
- How is benzene prepared from Ethyne? Give the reaction conditions.
- State the physical properties of Alkanes regarding their solubility.
- What is the 'Markovnikov’s Rule'?
- Draw the structural isomers of Butane (C4H10).
- Why is the staggered conformation of ethane more stable than the eclipsed form?
- Mention any two characteristics of aromatic compounds.
- Show the reaction for the preparation of ethane from Ethyl Bromide using Zinc and dil. HCl.
- Explain the 'Peroxide effect' (Anti-Markovnikov addition) in alkenes.
- Give the structural formula for Cyclobutane and Propane.
- Why do branched-chain alkanes have lower boiling points than straight-chain alkanes?
SECTION C: ANSWER IN BRIEF (30 Marks)
Answer any 10 out of 14 questions. (3 marks each)
- Describe the 'Wurtz Reaction' for the preparation of Alkanes.
- Explain the 'Friedel-Crafts Alkylation' of benzene with a chemical equation.
- Discuss the acidic nature of Alkynes compared to alkanes and alkenes.
- Explain the 'Nitration' of benzene, including the reagents used.
- Describe the preparation of Alkenes by the dehydration of alcohols.
- Illustrate the 'Newman Projections' for the eclipsed and staggered conformations of ethane.
- Write a note on the 'Pyrolysis' or 'Cracking' of alkanes.
- Explain the 'Directive Influence' of the hydroxyl group (-OH) in benzene.
- Describe the preparation of ethyne from Calcium Carbide.
- What is 'Geometrical Isomerism'? Why is it exhibited by alkenes?
- Give the step-by-step mechanism for the generation of a Nitronium ion (NO2+) in benzene nitration.
- Explain the 'Halogenation' of alkanes under UV light.
- Discuss the 'Resonance' structure of Benzene.
- Explain 'Ozonolysis' of Alkenes with a suitable example.
SECTION D: LONG ANSWERS (25 Marks)
Answer any 5 out of 7 questions. (5 marks each)
- Classify Hydrocarbons in detail with a flow chart and examples for each category.
- Explain in detail using both Sawhorse and Newman projections. Discuss their relative stability.
- Write chemical equations for: Hydrogenation, Halogenation, Hydrohalogenation, Hydration, and Hydroboration-Oxidation.
- Explain the general mechanism of Electrophilic Substitution in benzene, including the formation of the sigma-complex.
- Write the structures and IUPAC names of all five chain isomers of Hexane (C6H14).
- Explain Hydration (addition of H2O), Polymerization to form Benzene, and formation of metal alkynides.
- Compare the directive influence and activating/deactivating effects of Ortho-Para directing groups versus Meta directing groups.
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