Butadiene - Quiz
A) Hydrolysis B) Neutralization C) Polymerization D) Combustion
A) 1,4-addition B) 1,2-addition C) Substitution D) Elimination
A) Carbonyl complexes B) Hydride complexes C) Allyl complexes D) Nitrosyl complexes
A) Phthalic acid B) Butadiene oxide C) Cyclobutane D) Tetrahydrophthalic anhydride
A) Iron B) Molybdenum C) Nickel D) Palladium
A) Low B) Moderate C) Negligible D) High
A) Cardiovascular disease B) Glaucoma C) Arthritis D) Diabetes
A) Brain cancer B) Leukemia C) Bone cancer D) Skin cancer
A) Group 2B carcinogen B) Group 3 carcinogen C) Group 2A carcinogen D) Group 1 carcinogen
A) Confirmed human carcinogen B) Potent mutagen C) Suspected carcinogen D) Non-carcinogen
A) Nicotine B) Formaldehyde C) Acrylonitrile D) Benzene
A) Antioxidant B) Teratogen C) Allergen D) Neurotoxin
A) Children B) Men C) No gender difference D) Women
A) Differences in lung capacity B) Estrogen receptor impacts C) Body mass index D) Metabolic rate differences
A) Ability to acidify rain B) High solubility in water C) Contribution to smog visibility D) Potential to form ozone
A) OSHA B) FDA C) EPA D) TCEQ
A) calcium carbide B) n-butane C) acetylene D) ethanol
A) 2017 B) 1940 C) 1957 D) 1943
A) Lebedev process B) Steam cracking C) Houdry Catadiene process D) Ostromislensky process
A) Alumina and chromia B) Tantalum and silica C) Metal oxides only D) Calcium carbide
A) The Rubber Reserve Company B) Ivan Ostromislensky C) Houdry D) Sergey Lebedev
A) Calcium carbide and carbon dioxide B) Chromia and alumina C) Hydrogen and water D) Acetaldehyde and silica
A) 500–600 °C B) 325–350 °C C) 200–250 °C D) 400–450 °C
A) Ivan Ostromislensky B) None of the above C) Houdry D) Sergey Lebedev
A) Water B) Butene C) Acetaldehyde D) Hydrogen
A) Metal oxide B) Alumina and chromia C) Calcium carbide D) Tantalum-promoted porous silica
A) Acetylene B) Steam cracking C) n-Butane D) Ethanol only
A) None was produced B) It is the primary method C) It is used in Brazil only D) It is used in the US only
A) Higher output volumes B) Lower capital costs C) It uses cheaper catalysts D) Better efficiency than steam cracking
A) Russia, Europe, and India B) Houston, Institute, and Louisville C) Brazil, China, and India D) Borger, Toledo, and El Segundo
A) Higher capital costs B) Requires higher temperatures C) Not competitive for large volumes D) Lack of available catalysts
A) CH3-CH=CH-CH3 B) CH2=CH-CH=CH2 C) CH2=C=CH-CH3 D) CH2=CH2
A) Solid B) Metallic plasma C) Viscous liquid D) Colorless gas
A) Alkyne B) Conjugated diene C) Aromatic ring D) Alkane
A) Emission by motor vehicles B) Water treatment plants C) Agricultural runoff D) Natural volcanic activity
A) Eduard Tschunker B) Sergei Lebedev C) Walter Bock D) E. Caventou
A) Polymerized butadiene B) Isolated butadiene from petroleum C) Developed extractive distillation D) Invented steam cracking
A) Natural rubber B) Nitrile rubber C) Neoprene D) Silicone rubber
A) 14.2 million tons B) 5.5 million tons C) 20.1 million tons D) 8.8 million tons
A) Coal gasification B) Byproduct of steam cracking C) Fermentation of grain D) Direct synthesis from methane
A) Acetonitrile B) Ethanol C) Benzene D) Water
A) Methane B) Hydrogen gas C) Ethane D) Heavier feeds
A) A saturated alkane B) A conjugated diene C) An aromatic compound D) An allene
A) Before World War II B) After the Cold War C) During the Industrial Revolution D) In the early 19th century
A) It is a solid at room temperature B) It is highly toxic C) It has no industrial importance D) It is too expensive to produce
A) Chloroprene B) Adiponitrile C) Sulfolene D) Cyclohexene
A) Polymerization B) Dimerization C) Trimerization D) Hydrocyanation
A) Polybutadiene acrylonitrile (PBAN) B) Polybutadiene (PB) C) Acrylonitrile butadiene styrene (ABS) D) Styrene-butadiene (SBR)
A) Sulfolane B) Cyclododecatriene C) 1-octene D) Vinylcyclohexene
A) NBR B) SBR C) PBAN D) ABS
A) Nickel- or titanium-containing catalysts B) Copper-based catalysts C) Iron-based catalysts D) Palladium-based catalysts
A) 4-vinylcyclohexene B) Cyclooctadiene C) Cyclododecatriene D) 1-methoxy-2,7-octadiene
A) Sulfolane B) Chloroprene C) Adiponitrile D) 1-octene
A) SBR B) ABS C) HTPB D) NBR
A) Chlorine B) Hydrogen cyanide C) Sulfur dioxide D) Methanol
A) Torrance Industrial B) USSRP C) Petro-Tex D) Baton Rouge Chemicals
A) s-trans B) eclipsed C) s-cis D) gauche
A) 90° B) 180° C) 0° D) 38°
A) 38° B) 0° C) 180° D) 45°
A) 16.5 kJ/mol B) 3.5 kJ/mol C) 12.0 kJ/mol D) 24.8 kJ/mol
A) 180° B) 0° C) Around 38° D) 90°
A) 12.0 kJ/mol B) 24.8 kJ/mol C) 3.5 kJ/mol D) 16.5 kJ/mol
A) 3.5 kJ/mol B) 24.8 kJ/mol C) 12.0 kJ/mol D) 16.5 kJ/mol
A) Isolated double bonds B) A delocalized pi system C) High steric hindrance D) A completely single C-C bond
A) Hydrogenation B) Diels-Alder reaction C) Polymerization D) Combustion
A) 140.0 pm B) 133.0 pm C) 133.8 pm D) 120.0 pm
A) 30.3 kcal/mol B) 3.5 kcal/mol C) 57.1 kcal/mol D) 60.6 kcal/mol
A) VSEPR theory B) Valence Bond theory C) Resonance theory D) Hückel theory |
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