All Free Chemical Engineering MCQs with Answers

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6,983 questions · page 169 of 350

  • A. Dehydrogenation of naphthenes
  • B. Hydrogenation of naphthenes
  • C. Hydrocracking of paraffins
  • D. Saturation of olefins

Explanation: Catalytic reforming raises octane mainly by converting naphthenes into aromatic hydrocarbons with release of hydrogen, a dehydrogenation…

Correct answer: Dehydrogenation of naphthenes
  • A. 85
  • B. 65
  • C. 50
  • D. 98

Explanation: Catalytic reforming of naphtha normally gives a high reformate or gasoline yield, commonly around 80 to 90 percent by weight.

Correct answer: 85
  • A. Lighter paraffins
  • B. Olefins and aromatics
  • C. Stabilised gasoline
  • D. Diesel

Explanation: Pyrolysis cracks kerosene or natural gasoline at high temperature into smaller unsaturated molecules and ring compounds, producing mainly…

Correct answer: Olefins and aromatics
  • A. Alumina
  • B. Nickel
  • C. Silica gel
  • D. Sulphuric acid

Explanation: Sulphuric acid is a liquid acid catalyst commonly used in alkylation to combine light olefins with isoparaffins.

Correct answer: Sulphuric acid
  • A. An endothermic reaction
  • B. An exothermic reaction
  • C. Favoured at very low temperature
  • D. None of these

Explanation: Cracking breaks large hydrocarbon molecules into smaller ones and requires heat to rupture their bonds, so it is endothermic.

Correct answer: An endothermic reaction
  • A. Less than 90% promotes polymerisation
  • B. Both A. and B.
  • C. More than 98% promotes cracking
  • D. Neither A. nor B.

Explanation: Acid that is too dilute, below about 90%, encourages polymerisation of olefins, while excessively concentrated acid can promote…

Correct answer: Both A. and B.
  • A. H2SO4
  • B. H3PO4
  • C. AlCl3
  • D. HF

Explanation: Aluminium chloride, usually with hydrogen chloride, is the classical catalyst system for hydrocarbon isomerisation.

Correct answer: AlCl3
  • A. Olefins into paraffins
  • B. Naphthenes into paraffin
  • C. Naphthenes into olefins
  • D. Naphthenes into aromatics

Explanation: In catalytic reforming, cycloalkanes or naphthenes undergo dehydrogenation to form aromatic hydrocarbons, often with hydrogen as a…

Correct answer: Naphthenes into aromatics
  • A. Dehydrogenation of lower paraffins
  • B. Dehydrogenation of Naphthene
  • C. Dehydrocyclization of higher paraffins
  • D. Isomerisation of paraffins

Explanation: Catalytic reforming favorably dehydrogenates naphthenes, dehydrocyclizes suitable paraffins and isomerizes hydrocarbons to raise octane…

Correct answer: Dehydrogenation of lower paraffins
  • A. 10 atm & 500°C
  • B. 2 atm & 500°C
  • C. 30 atm & 200°C
  • D. 50 atm & 750°C

Explanation: Fluid catalytic cracking commonly uses temperatures near 500°C and relatively low pressures, around 1–3 atm, because cracking is favoured…

Correct answer: 2 atm & 500°C
  • A. Gasoline obtained has a very low octane number
  • B. Pressure & temperature is very high
  • C. Gasoline obtained has very high amount of gum forming compounds
  • D. Gasoline obtained has very high aromatic content

Explanation: Catalytic cracking promotes dehydrogenation, cyclisation and aromatisation, so its gasoline generally has a high octane number and…

Correct answer: Gasoline obtained has very high aromatic content
  • A. Non-elementary
  • B. Multiple
  • C. Autocatalytic
  • D. Elementary

Explanation: For an elementary reaction, the rate equation follows directly from the stoichiometric equation.

Correct answer: Non-elementary
  • A. Is independent of temperature
  • B. Both B. and C.
  • C. Depends on the nature of the reactants
  • D. Varies with temperature

Explanation: The rate constant changes with temperature according to the Arrhenius relationship and also depends on the reacting species and reaction…

Correct answer: Both B. and C.
  • A. 1
  • B. 2
  • C. 3
  • D. 4

Explanation: For a second-order reaction, the time required for a fixed fractional conversion is proportional to 1/C₀.

Correct answer: 2
  • A. Nature of the reactants
  • B. Concentration of the reactants
  • C. Temperature at which the reaction is carried
  • D. All A., B. and C.

Explanation: Reaction velocity is affected by the chemical nature of the reactants, their concentrations, and temperature.

Correct answer: All A., B. and C.
  • A. Catalytic cracking
  • B. Methanol synthesis
  • C. Ammonia synthesis
  • D. Oxidation of sulphur

Explanation: Catalytic cracking requires heat to break large hydrocarbon molecules into smaller ones, so it is endothermic.

Correct answer: Catalytic cracking
  • A. Series of CSTR
  • B. Plug flow reactor
  • C. Backmix reactor
  • D. PFR in series

Explanation: When high reactant concentration improves yield, backmixing is undesirable because a CSTR operates throughout at the lower exit…

Correct answer: Backmix reactor
  • A. Mixing takes place in axial direction only
  • B. Residence time is constant
  • C. Condition similar to plug flow reactor exists
  • D. Velocity of reaction can be controlled

Explanation: A semi-batch reactor permits controlled addition or removal of reactants during operation, so the reaction rate can be adjusted through…

Correct answer: Velocity of reaction can be controlled