Alkanes: Structure and Properties
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Questions and Answers

What is the hybridization of the orbitals in alkanes?

  • sp3 hybridization (correct)
  • sp2 hybridization
  • sp hybridization
  • d2sp3 hybridization
  • What is the bond angle in the tetrahedral arrangement of sp3 hybridized carbon in alkanes?

  • 180º
  • 90º
  • 109.5º (correct)
  • 120º
  • Why is the process of promoting an electron to a p orbital considered favourable?

  • It results in a complete valence shell.
  • It creates more stable ionic bonds.
  • It allows for unpaired electrons which reduce repulsion. (correct)
  • It leads to a decrease in total energy.
  • What is the electronic configuration of carbon before hybridization?

    <p>1s2 2s2 2p2</p> Signup and view all the answers

    What type of bond is formed between the sp3 orbital of carbon and the 1s orbital of hydrogen in alkanes?

    <p>Covalent bond</p> Signup and view all the answers

    What is produced from every carbon and two hydrogen atoms in a hydrocarbon during combustion?

    <p>Carbon dioxide and water</p> Signup and view all the answers

    Which of the following emissions from internal combustion engines does NOT contribute to acid rain?

    <p>Carbon dioxide</p> Signup and view all the answers

    What is the primary function of a catalytic converter in vehicles?

    <p>To convert harmful emissions into less harmful substances</p> Signup and view all the answers

    What happens when leaded petrol passes through a catalytic converter?

    <p>Lead deposits poison the catalyst.</p> Signup and view all the answers

    Which process involves the unequal splitting of shared electron pairs in covalent bonds?

    <p>Heterolysis</p> Signup and view all the answers

    Which bond is broken first in a reaction involving alkanes and chlorine?

    <p>Cl-Cl bond</p> Signup and view all the answers

    What is produced when a methyl radical reacts with a chlorine molecule?

    <p>Chlorine radical</p> Signup and view all the answers

    What role do free radicals play in the reaction between alkanes and chlorine?

    <p>They initiate and propagate the reaction.</p> Signup and view all the answers

    What happens during the termination step in the reaction involving free radicals?

    <p>Free radicals are removed.</p> Signup and view all the answers

    Why are free radicals considered very reactive?

    <p>They seek to gain an additional bond to stabilize themselves.</p> Signup and view all the answers

    What is the primary role of chlorine radicals in the reaction process?

    <p>To propagate the reaction and regenerate themselves</p> Signup and view all the answers

    Which of the following statements is NOT true about the reaction mechanism described?

    <p>Termination results in the formation of additional radicals.</p> Signup and view all the answers

    What initiates the homolytic fission of covalent bonds to form free radicals?

    <p>Shining UV light onto the mixture</p> Signup and view all the answers

    What is formed as a result of termination when two chlorine radicals combine?

    <p>Chlorine gas (Cl2)</p> Signup and view all the answers

    What is the outcome when excess chlorine is used during the chlorination process?

    <p>A variety of chlorinated products will be obtained</p> Signup and view all the answers

    Which product is primarily produced through the thermal cracking process?

    <p>Ethene</p> Signup and view all the answers

    Which condition is NOT associated with the thermal cracking process?

    <p>Presence of a catalyst</p> Signup and view all the answers

    What is the effect of fractional distillation in the context of chlorination reactions?

    <p>It separates individual haloalkanes from the reaction mixture</p> Signup and view all the answers

    What type of mechanism does catalytic cracking proceed through?

    <p>Carbocation mechanism</p> Signup and view all the answers

    Which of the following fractions is primarily used as aviation fuel?

    <p>Kerosene</p> Signup and view all the answers

    What is the general formula for non-cyclic alkanes?

    <p>C_nH_{2n+2}</p> Signup and view all the answers

    What property allows for the separation of crude petroleum into fractions?

    <p>Fractional distillation based on boiling point</p> Signup and view all the answers

    Which type of fission is involved in the catalytic cracking process?

    <p>Heterolytic fission</p> Signup and view all the answers

    Which of the following is NOT a use of alkanes?

    <p>Source of antioxidants</p> Signup and view all the answers

    What condition is necessary for thermal cracking to occur effectively?

    <p>High temperature</p> Signup and view all the answers

    What product can be formed from the cracking of heavy fractions?

    <p>Aromatic hydrocarbons</p> Signup and view all the answers

    Study Notes

    Structure of Alkanes

    • Members of a homologous series.
    • General formula is CnH2n+2 (for non-cyclic alkanes).
    • Saturated hydrocarbons, meaning all carbon-carbon bonding is single.
    • Bonds are spaced tetrahedrally about carbon atoms.

    Physical properties of Alkanes

    • Boiling point increases with increasing chain length (due to increased Van der Waals forces).
    • Alkanes are insoluble in water (due to their non-polar nature).
    • Alkanes are less dense than water.

    Chemical properties of Alkanes

    • Relatively unreactive due to strong C-H and C-C bonds.
    • They undergo combustion reactions, releasing energy.
    • They undergo substitution reactions, replacing hydrogen atoms with other atoms or groups.

    Breaking covalent bonds

    • Can occur via homolytic fission (producing radicals) or heterolytic fission (producing ions).
    • The weakest bond is usually broken first.
    • Energy to break bonds can come from heat or light.

    Cracking

    • Involves breaking C-C bonds in alkanes to convert heavier fractions into lighter, more useful products (like gasoline).
    • Two types:
      • Thermal cracking:
        • Uses high pressure (7000 kPa) and high temperature (400°C - 900°C).
        • Proceeds via a free radical mechanism.
        • Produces mainly alkenes and hydrogen.
      • Catalytic cracking:
        • Uses zeolite catalyst, slight pressure, and high temperature (450°C).
        • Proceeds via a carbocation (ionic) mechanism.
        • Produces branched and cyclic alkanes, aromatic hydrocarbons.

    Uses of Alkanes

    • LPG is used as fuel for cooking and heating.
    • Gasoline is used as fuel for cars.
    • Naphtha is used to make petrochemicals.
    • Kerosine is used as aviation fuel.
    • Gas oil is used as central heating fuel.
    • Lubricating oil is used for lubrication.
    • Fuel oil is used as power station fuel and ship fuel.
    • Wax and grease are used in candles and as grease for bearings.
    • Bitumen is used in road surfaces and roofing.

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    Description

    Explore the structure, physical, and chemical properties of alkanes in this comprehensive quiz. Understand the implications of their saturated nature, physical characteristics, and reactions they undergo, including combustion and substitution. Test your knowledge on breaking covalent bonds and the process of cracking.

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