{"product_id":"hydrocarbon-chemistry-2-volume-set-isbn-9781119390510","title":"Hydrocarbon Chemistry, 2 Volume Set","description":"This book provides an unparalleled contemporary assessment of hydrocarbon chemistry – presenting basic concepts, current research, and future applications.\u003cbr\u003e\u003cbr\u003e•    Comprehensive and updated review and discussion of the field of hydrocarbon chemistry\u003cbr\u003e•    Includes literature coverage since the publication of the previous edition\u003cbr\u003e•    Expands or adds coverage of: carboxylation, sustainable hydrocarbons, extraterrestrial hydrocarbons\u003cbr\u003e•    Addresses a topic of special relevance in contemporary science, since hydrocarbons play a role as a possible replacement for coal, petroleum oil, and natural gas as well as their environmentally safe use\u003cbr\u003e•    Reviews of prior edition: “...literature coverage is comprehensive and ideal for quickly reviewing specific topics...of most value to industrial chemists...” (Angewandte Chemie) and “...useful for chemical engineers as well as engineers in the chemical and petrochemical industries.” (Petroleum Science and Technology) \u003cp\u003e\u003cb\u003eVolume 1\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003ePreface to the Third Edition xiii\u003c\/p\u003e \u003cp\u003ePreface to the Second Edition xv\u003c\/p\u003e \u003cp\u003ePreface to the First Edition xvii\u003c\/p\u003e \u003cp\u003eIntroduction xix\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIntroduction and General Aspects 1\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1.1 Hydrocarbons and Their Classes 1\u003c\/p\u003e \u003cp\u003e1.2 Energy–Hydrocarbon Relationships 2\u003c\/p\u003e \u003cp\u003e1.3 Hydrocarbon Sources 4\u003c\/p\u003e \u003cp\u003eExtraterrestrial Hydrocarbons 15\u003c\/p\u003e \u003cp\u003e1.4 Hydrocarbon Production from Natural Sources 16\u003c\/p\u003e \u003cp\u003e1.5 Hydrocarbon Synthesis 20\u003c\/p\u003e \u003cp\u003e1.6 Nonrenewable and Renewable Hydrocarbons 27\u003c\/p\u003e \u003cp\u003e1.7 Regenerative Hydrocarbons from CO2 Emission Capture and Recycling 29\u003c\/p\u003e \u003cp\u003e1.8 Hydrocarbon Functionalization Reactions 30\u003c\/p\u003e \u003cp\u003e1.9 Use of Hydrocarbons, Petroleum Oil 35\u003c\/p\u003e \u003cp\u003e1.9.1 Energy Generation, Storage, and Delivery: Heating 36\u003c\/p\u003e \u003cp\u003e1.9.2 Transportation Fuels 36\u003c\/p\u003e \u003cp\u003e1.9.3 Chemical Products, Plastics, and Pharmaceuticals 38\u003c\/p\u003e \u003cp\u003eReferences 38\u003c\/p\u003e \u003cp\u003e\u003cb\u003eHydrocarbons from Petroleum and Natural Gas 49\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e2.1 Cracking 49\u003c\/p\u003e \u003cp\u003e2.2 Reforming 62\u003c\/p\u003e \u003cp\u003eHydroforming 64\u003c\/p\u003e \u003cp\u003eMetal-Catalyzed Reforming 65\u003c\/p\u003e \u003cp\u003e2.3 Dehydrogenation with Olefin Production 71\u003c\/p\u003e \u003cp\u003eHeterogeneous Catalysts 73\u003c\/p\u003e \u003cp\u003eHomogeneous Catalysts 78\u003c\/p\u003e \u003cp\u003eC2–C3 Alkenes 85\u003c\/p\u003e \u003cp\u003eC4 Alkenes 86\u003c\/p\u003e \u003cp\u003eButa-1,3-diene and Isoprene 87\u003c\/p\u003e \u003cp\u003eHigher Olefins 88\u003c\/p\u003e \u003cp\u003eStyrene 88\u003c\/p\u003e \u003cp\u003e2.4 Upgrading of Natural-Gas Liquids 89\u003c\/p\u003e \u003cp\u003e2.5 Aromatics Production 89\u003c\/p\u003e \u003cp\u003eReferences 102\u003c\/p\u003e \u003cp\u003e\u003cb\u003eSynthesis from C Sources 125\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e3.1 Aspects of C1 Chemistry 126\u003c\/p\u003e \u003cp\u003e3.2 Chemical Reduction to Methanol and Oxygenates; Recycling of CO2 127\u003c\/p\u003e \u003cp\u003eHeterogeneous Hydrogenation 129\u003c\/p\u003e \u003cp\u003eHomogeneous Hydrogenation 137\u003c\/p\u003e \u003cp\u003eIonic Reduction 143\u003c\/p\u003e \u003cp\u003eElectrochemical and Electrocatalytic Reduction 143\u003c\/p\u003e \u003cp\u003ePhotoreduction 146\u003c\/p\u003e \u003cp\u003eEnzymatic Reduction 148\u003c\/p\u003e \u003cp\u003e3.3 Fischer–Tropsch Chemistry 149\u003c\/p\u003e \u003cp\u003e3.4 Oxygenation of Methane 166\u003c\/p\u003e \u003cp\u003eMethanol Synthesis 166\u003c\/p\u003e \u003cp\u003e3.5 Oligocondensation of Methane 173\u003c\/p\u003e \u003cp\u003e3.6 Hydrocarbons from Methane Derivatives 186\u003c\/p\u003e \u003cp\u003eMethanol Conversion to Hydrocarbons 186\u003c\/p\u003e \u003cp\u003eMethanol to Hydrocarbon Technologies 196\u003c\/p\u003e \u003cp\u003eMethanol to Gasoline 196\u003c\/p\u003e \u003cp\u003eMethanol to Olefin 197\u003c\/p\u003e \u003cp\u003eMethanol to Propylene 198\u003c\/p\u003e \u003cp\u003eReferences 200\u003c\/p\u003e \u003cp\u003e\u003cb\u003eIsomerization 237\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e4.1 Acid-Catalyzed and Bifunctional Isomerization 238\u003c\/p\u003e \u003cp\u003eMechanism 243\u003c\/p\u003e \u003cp\u003eSide-Chain Isomerization 250\u003c\/p\u003e \u003cp\u003ePositional Isomerization 250\u003c\/p\u003e \u003cp\u003e4.2 Base-Catalyzed Isomerization 262\u003c\/p\u003e \u003cp\u003e4.2.1 Alkenes 262\u003c\/p\u003e \u003cp\u003e4.3 Metal-Catalyzed Isomerization 266\u003c\/p\u003e \u003cp\u003e4.4 Pericyclic Rearrangements 277\u003c\/p\u003e \u003cp\u003e4.5 Practical Applications 284\u003c\/p\u003e \u003cp\u003eAlkanes 284\u003c\/p\u003e \u003cp\u003eAlkenes 285\u003c\/p\u003e \u003cp\u003e4.5.2 Isomerization of Xylenes 286\u003c\/p\u003e \u003cp\u003eReferences 287\u003c\/p\u003e \u003cp\u003e\u003cb\u003eAlkylations 305\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e5.1 Acid-Catalyzed Alkylation 305\u003c\/p\u003e \u003cp\u003eAlkylolysis (Alkylative Cleavage) 317\u003c\/p\u003e \u003cp\u003eAlkylation of Alkenes with Organic Halides 318\u003c\/p\u003e \u003cp\u003eAlkylation of Alkynes 320\u003c\/p\u003e \u003cp\u003eAlkylation with Carbonyl Compounds: The Prins Reaction 320\u003c\/p\u003e \u003cp\u003eCatalysts 324\u003c\/p\u003e \u003cp\u003eAlkylation with Alkyl Halides 326\u003c\/p\u003e \u003cp\u003eAlkylation with Alkenes 331\u003c\/p\u003e \u003cp\u003eAlkylation with Alkanes 335\u003c\/p\u003e \u003cp\u003eAlkylation with Other Reagents 338\u003c\/p\u003e \u003cp\u003e5.2 Base-Catalyzed Alkylation 350\u003c\/p\u003e \u003cp\u003e5.3 Alkylation through Organometallics 352\u003c\/p\u003e \u003cp\u003e5.4 Miscellaneous Alkylations 356\u003c\/p\u003e \u003cp\u003e5.5 Practical Applications 360\u003c\/p\u003e \u003cp\u003eReferences 369\u003c\/p\u003e \u003cp\u003e\u003cb\u003eAddition Reactions 389\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e6.1 Hydration 389\u003c\/p\u003e \u003cp\u003eProduction of Alcohols by Hydration of Alkenes 395\u003c\/p\u003e \u003cp\u003eProduction of Octane-Enhancing Oxygenates 396\u003c\/p\u003e \u003cp\u003eAcetaldehyde 397\u003c\/p\u003e \u003cp\u003e6.2 HX Addition 398\u003c\/p\u003e \u003cp\u003eAlkenes 398\u003c\/p\u003e \u003cp\u003eDienes 403\u003c\/p\u003e \u003cp\u003eAlkynes 404\u003c\/p\u003e \u003cp\u003eEthyl Chloride 411\u003c\/p\u003e \u003cp\u003eHydrochlorination of Buta-1,3-diene 411\u003c\/p\u003e \u003cp\u003eVinyl Chloride 411\u003c\/p\u003e \u003cp\u003eEthylene Chlorohydrin 412\u003c\/p\u003e \u003cp\u003ePropylene Chlorohydrin 412\u003c\/p\u003e \u003cp\u003eAdiponitrile 412\u003c\/p\u003e \u003cp\u003eAcrylonitrile 413\u003c\/p\u003e \u003cp\u003e6.3 Halogen Addition 413\u003c\/p\u003e \u003cp\u003eVinyl Chloride 422\u003c\/p\u003e \u003cp\u003eChlorination of Buta-1,3-diene 424\u003c\/p\u003e \u003cp\u003e6.4 Addition to Form C–N Bonds 424\u003c\/p\u003e \u003cp\u003e6.5 Addition to Form C–O, C–S, and C–P Bonds 433\u003c\/p\u003e \u003cp\u003e6.6 Hydrometalation 439\u003c\/p\u003e \u003cp\u003eAlkenes 440\u003c\/p\u003e \u003cp\u003eDienes 446\u003c\/p\u003e \u003cp\u003eAlkynes 448\u003c\/p\u003e \u003cp\u003eAlkenes 452\u003c\/p\u003e \u003cp\u003eDienes 456\u003c\/p\u003e \u003cp\u003eAlkynes 457\u003c\/p\u003e \u003cp\u003e6.7 Halometalation 462\u003c\/p\u003e \u003cp\u003e6.8 Solvometalation 465\u003c\/p\u003e \u003cp\u003e6.9 Carbometalation 466\u003c\/p\u003e \u003cp\u003e6.10 Cycloaddition 471\u003c\/p\u003e \u003cp\u003eReferences 477\u003c\/p\u003e \u003cp\u003e\u003cb\u003eCarbonylation and Carboxylation 509\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e7.1 Carbonylation 509\u003c\/p\u003e \u003cp\u003eHydroformylation in Biphasic Solvent Systems 515\u003c\/p\u003e \u003cp\u003eThe Use of Heterogeneous Catalysts 516\u003c\/p\u003e \u003cp\u003eHydroformylation of Higher Alkenes 518\u003c\/p\u003e \u003cp\u003eHydroformylation of Internal Alkenes 519\u003c\/p\u003e \u003cp\u003eAsymmetric Hydroformylation 520\u003c\/p\u003e \u003cp\u003e7.2 Carboxylation 533\u003c\/p\u003e \u003cp\u003eSaturated Hydrocarbons 534\u003c\/p\u003e \u003cp\u003eAromatic Hydrocarbons 536\u003c\/p\u003e \u003cp\u003eHydrocarboxylation and hydroesterification 539\u003c\/p\u003e \u003cp\u003eAminocarboxylation 545\u003c\/p\u003e \u003cp\u003eNeocarboxylic Acids 547\u003c\/p\u003e \u003cp\u003eHydrocarboxymethylation of Long-Chain Alkenes 547\u003c\/p\u003e \u003cp\u003ePropionic Acid 547\u003c\/p\u003e \u003cp\u003eAcrylic Acid and Acrylates 548\u003c\/p\u003e \u003cp\u003eReferences 548\u003c\/p\u003e \u003cp\u003e\u003cb\u003eAcylation 569\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e8.1 Acylation of Aromatics 569\u003c\/p\u003e \u003cp\u003eNew Soluble Catalysts 573\u003c\/p\u003e \u003cp\u003eSolid Catalysts 575\u003c\/p\u003e \u003cp\u003eThe Gattermann–Koch Reaction 577\u003c\/p\u003e \u003cp\u003eThe Gattermann Reaction 579\u003c\/p\u003e \u003cp\u003eOther Formylations 580\u003c\/p\u003e \u003cp\u003e8.2 Acylation of Aliphatic Compounds 581\u003c\/p\u003e \u003cp\u003eReferences 586\u003c\/p\u003e \u003cp\u003eIndex 000\u003c\/p\u003e \u003cp\u003e\u003cb\u003eVolume 2\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003ePreface to the Third Edition xi\u003c\/p\u003e \u003cp\u003ePreface to the Second Edition xiii\u003c\/p\u003e \u003cp\u003ePreface to the First Edition xv\u003c\/p\u003e \u003cp\u003eIntroduction xvii\u003c\/p\u003e \u003cp\u003e\u003cb\u003eOxidation–Oxygenation 593\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e9.1 Oxidation of Alkanes 594\u003c\/p\u003e \u003cp\u003eAutoxidation of Alkanes 594\u003c\/p\u003e \u003cp\u003eOxidation of Methane 596\u003c\/p\u003e \u003cp\u003eOxidation with Stoichiometric Oxidants 606\u003c\/p\u003e \u003cp\u003eOxidation Catalyzed by Enzymes and Metalloporphyrins 613\u003c\/p\u003e \u003cp\u003eMetal-Catalyzed Oxidation in the Homogeneous Phase 616\u003c\/p\u003e \u003cp\u003eOxidation Induced by Heterogeneous Catalysts 619\u003c\/p\u003e \u003cp\u003eMetal Oxidants 623\u003c\/p\u003e \u003cp\u003eElectrophilic Reagents 624\u003c\/p\u003e \u003cp\u003eOxygenolysis 628\u003c\/p\u003e \u003cp\u003e9.2 Oxidation of Alkenes 630\u003c\/p\u003e \u003cp\u003eDirect Oxidation with Stoichiometric Oxidants 630\u003c\/p\u003e \u003cp\u003eMetal-Catalyzed Epoxidation 635\u003c\/p\u003e \u003cp\u003eEpoxidation Catalyzed by Metalloporphyrins 644\u003c\/p\u003e \u003cp\u003eAsymmetric Epoxidation 647\u003c\/p\u003e \u003cp\u003eAutoxidation 650\u003c\/p\u003e \u003cp\u003eReactions with Singlet Oxygen 650\u003c\/p\u003e \u003cp\u003eBis-Hydroxylation 656\u003c\/p\u003e \u003cp\u003eBis-Acetoxylation 663\u003c\/p\u003e \u003cp\u003eOxidation with Palladium in the Homogeneous Phase 664\u003c\/p\u003e \u003cp\u003eOxidation with Other Reagents 669\u003c\/p\u003e \u003cp\u003eVinylic Acetoxylation 671\u003c\/p\u003e \u003cp\u003eOzonation 673\u003c\/p\u003e \u003cp\u003eMechanism 673\u003c\/p\u003e \u003cp\u003eSynthetic Applications 676\u003c\/p\u003e \u003cp\u003eOther Oxidants 678\u003c\/p\u003e \u003cp\u003eAllylic Hydroxylation and Acyloxylation 681\u003c\/p\u003e \u003cp\u003eOxidation to α,β-Unsaturated Carbonyl Compounds 686\u003c\/p\u003e \u003cp\u003e9.3 Oxidation of Alkynes 690\u003c\/p\u003e \u003cp\u003e9.4 Oxidation of Aromatics 693\u003c\/p\u003e \u003cp\u003eOxidation to Phenols 693\u003c\/p\u003e \u003cp\u003eRing Acyloxylation 701\u003c\/p\u003e \u003cp\u003eOxidation to Quinones 702\u003c\/p\u003e \u003cp\u003eOxidation to Arene Oxides and Arene Diols 703\u003c\/p\u003e \u003cp\u003eOxidation with Singlet Oxygen 704\u003c\/p\u003e \u003cp\u003eOxidation of Methyl-Substituted Aromatics 706\u003c\/p\u003e \u003cp\u003eOxidation of Other Arenes 708\u003c\/p\u003e \u003cp\u003eBenzylic Acetoxylation 711\u003c\/p\u003e \u003cp\u003e9.5 Practical Applications 712\u003c\/p\u003e \u003cp\u003eAcetic Acid 712\u003c\/p\u003e \u003cp\u003eMaleic Anhydride 713\u003c\/p\u003e \u003cp\u003eOxidation of Cyclohexane 715\u003c\/p\u003e \u003cp\u003eOxidation of Cyclododecane 715\u003c\/p\u003e \u003cp\u003esec-Alcohols 715\u003c\/p\u003e \u003cp\u003eEthylene Oxide 716\u003c\/p\u003e \u003cp\u003ePropylene Oxide 718\u003c\/p\u003e \u003cp\u003eAcetaldehyde and Acetone 719\u003c\/p\u003e \u003cp\u003eVinyl Acetate 719\u003c\/p\u003e \u003cp\u003e1,4-Diacetoxybut-2-ene 720\u003c\/p\u003e \u003cp\u003eAcrolein and Acrylic Acid 720\u003c\/p\u003e \u003cp\u003eMethacrolein and Methacrylic Acid 721\u003c\/p\u003e \u003cp\u003eAcrylonitrile 721\u003c\/p\u003e \u003cp\u003eOther Processes 722\u003c\/p\u003e \u003cp\u003ePhenol and Acetone 722\u003c\/p\u003e \u003cp\u003eBenzoic Acid 723\u003c\/p\u003e \u003cp\u003eTerephthalic Acid 723\u003c\/p\u003e \u003cp\u003eMaleic Anhydride 724\u003c\/p\u003e \u003cp\u003ePhthalic Anhydride 725\u003c\/p\u003e \u003cp\u003eAnthraquinone 727\u003c\/p\u003e \u003cp\u003eReferences 727\u003c\/p\u003e \u003cp\u003e\u003cb\u003eHeterosubstitution 795\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e10.1 Electrophilic (Acid-Catalyzed) Substitution 795\u003c\/p\u003e \u003cp\u003eHalogenation 796\u003c\/p\u003e \u003cp\u003eNitration 798\u003c\/p\u003e \u003cp\u003eSulfuration 799\u003c\/p\u003e \u003cp\u003eHalogenation 800\u003c\/p\u003e \u003cp\u003eNitration 804\u003c\/p\u003e \u003cp\u003eSulfonation 808\u003c\/p\u003e \u003cp\u003eSynthesis of Sulfoxides and Sulfones 810\u003c\/p\u003e \u003cp\u003eChlorobenzene 811\u003c\/p\u003e \u003cp\u003eNitration of Benzene and Toluene 811\u003c\/p\u003e \u003cp\u003eSulfonation of Benzene and Alkylbenzenes 811\u003c\/p\u003e \u003cp\u003e10.2 Free-Radical Substitution 812\u003c\/p\u003e \u003cp\u003eChlorination 812\u003c\/p\u003e \u003cp\u003eFluorination 817\u003c\/p\u003e \u003cp\u003eBromination 818\u003c\/p\u003e \u003cp\u003eIodination 819\u003c\/p\u003e \u003cp\u003eSide-Chain Halogenation of Arylalkanes 819\u003c\/p\u003e \u003cp\u003eChlorination of Alkanes 824\u003c\/p\u003e \u003cp\u003eSide-Chain Chlorination of Toluene 826\u003c\/p\u003e \u003cp\u003eUnsaturated Chlorides 826\u003c\/p\u003e \u003cp\u003eSulfochlorination of Alkanes 827\u003c\/p\u003e \u003cp\u003eNitroalkanes 827\u003c\/p\u003e \u003cp\u003e10.3 Formation of C–N Bonds 827\u003c\/p\u003e \u003cp\u003e10.4 Formation of Carbon–Metal Bonds 831\u003c\/p\u003e \u003cp\u003eBorylation 837\u003c\/p\u003e \u003cp\u003eSilylation 840\u003c\/p\u003e \u003cp\u003eAl, Ge, and Sn Derivatives 841\u003c\/p\u003e \u003cp\u003e10.5 Miscellaneous Derivatives 842\u003c\/p\u003e \u003cp\u003eReferences 843\u003c\/p\u003e \u003cp\u003e\u003cb\u003eReduction–Hydrogenation 863\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e11.1 Heterogeneous Catalytic Hydrogenation 864\u003c\/p\u003e \u003cp\u003eMechanism 866\u003c\/p\u003e \u003cp\u003eStereochemistry 870\u003c\/p\u003e \u003cp\u003e11.2 Homogeneous Catalytic Hydrogenation 886\u003c\/p\u003e \u003cp\u003eMechanism 891\u003c\/p\u003e \u003cp\u003eSelectivity and Stereochemistry 893\u003c\/p\u003e \u003cp\u003eAsymmetric Hydrogenation 896\u003c\/p\u003e \u003cp\u003e11.3 Transfer Hydrogenation 904\u003c\/p\u003e \u003cp\u003e11.4 Chemical and Electrochemical Reduction 906\u003c\/p\u003e \u003cp\u003eMechanism 911\u003c\/p\u003e \u003cp\u003eSelectivity 911\u003c\/p\u003e \u003cp\u003e11.5 Ionic Hydrogenation 913\u003c\/p\u003e \u003cp\u003e11.6 Hydrogenolysis of Saturated Hydrocarbons 918\u003c\/p\u003e \u003cp\u003e11.7 Practical Applications 931\u003c\/p\u003e \u003cp\u003eC2 Hydrorefining 931\u003c\/p\u003e \u003cp\u003eC3 Hydrorefining 931\u003c\/p\u003e \u003cp\u003eC4 Hydrorefining 931\u003c\/p\u003e \u003cp\u003eGasoline Hydrorefining 932\u003c\/p\u003e \u003cp\u003eReferences 934\u003c\/p\u003e \u003cp\u003e\u003cb\u003eMetathesis 959\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e12.1 Metathesis of Acyclic Alkenes 960\u003c\/p\u003e \u003cp\u003e12.2 Alkane Metathesis 973\u003c\/p\u003e \u003cp\u003e12.3 Metathesis of Alkynes 976\u003c\/p\u003e \u003cp\u003e12.4 Ring-Closing Metathesis 978\u003c\/p\u003e \u003cp\u003e12.5 Ring-Opening Metathesis and Ring-Opening Metathesis Polymerization 979\u003c\/p\u003e \u003cp\u003e12.6 Practical Applications 983\u003c\/p\u003e \u003cp\u003eReferences 986\u003c\/p\u003e \u003cp\u003e\u003cb\u003eOligomerization and Polymerization 1001\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e13.1 Oligomerization 1001\u003c\/p\u003e \u003cp\u003ePractical Applications 1006\u003c\/p\u003e \u003cp\u003eAlkenes 1008\u003c\/p\u003e \u003cp\u003eAlkynes 1013\u003c\/p\u003e \u003cp\u003eCyclooligomerization 1014\u003c\/p\u003e \u003cp\u003ePractical Applications 1018\u003c\/p\u003e \u003cp\u003e13.2 Polymerization 1021\u003c\/p\u003e \u003cp\u003eZiegler–Natta Catalysts 1038\u003c\/p\u003e \u003cp\u003eThe Phillips Catalyst 1041\u003c\/p\u003e \u003cp\u003eGroup IV Metallocene Catalysts 1042\u003c\/p\u003e \u003cp\u003ePostmetallocene Catalysts 1047\u003c\/p\u003e \u003cp\u003eStereoregular Polymerization of Propylene 1058\u003c\/p\u003e \u003cp\u003eIsospecific Polymerization 1059\u003c\/p\u003e \u003cp\u003eSyndiospecific Polymerization 1064\u003c\/p\u003e \u003cp\u003eStereoregular Polymerization of Dienes 1065\u003c\/p\u003e \u003cp\u003eEthylene Polymers 1072\u003c\/p\u003e \u003cp\u003ePolypropylene 1074\u003c\/p\u003e \u003cp\u003ePolybutylenes 1075\u003c\/p\u003e \u003cp\u003eStyrene Polymers 1076\u003c\/p\u003e \u003cp\u003ePolydienes 1077\u003c\/p\u003e \u003cp\u003eReferences 1078\u003c\/p\u003e \u003cp\u003e\u003cb\u003eOutlook 1111\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e14.1 Sustainable Hydrocarbon Chemistry for the Future 1111\u003c\/p\u003e \u003cp\u003e14.2 Extraterrestrial Hydrocarbon Chemistry 1114\u003c\/p\u003e \u003cp\u003eReferences 1115\u003c\/p\u003e \u003cp\u003eIndex 000\u003c\/p\u003e   \u003cp\u003e\u003cb\u003e GEORGE A. OLAH, PhD,\u003c\/b\u003e was awarded the undivided 1994 Nobel Prize in Chemistry. He was a Distinguished Professor of Chemistry, Chemical Engineering and Materials Science; Donald P. and Katherine B. Loker Chair in Organic Chemistry; and Founding Director of the Loker Hydrocarbon Research Institute at the University of Southern California, Los Angeles. He passed away on March 8, 2017.   \u003c\/p\u003e\u003cp\u003e\u003cb\u003e ÁRPÁD MOLNÁR, DSc,\u003c\/b\u003e is an Emeritus Professor at the University of Szeged, Hungary, and a Senior Fellow of the Loker Hydrocarbon Research Institute at the University of Southern California.   \u003c\/p\u003e\u003cp\u003e\u003cb\u003e G. K. SURYA PRAKASH, PhD,\u003c\/b\u003e is the George A. and Judith A. Olah Nobel Laureate Chair Professor and the Director of the Loker Hydrocarbon Research Institute at the University of Southern California.    \u003c\/p\u003e\u003cp\u003eReviews of the 2nd Edition:\u003c\/p\u003e \u003cp\u003e\"...literature coverage is comprehensive and ideal for quickly reviewing specific topics... of most value to industrial chemists...\"\u003c\/p\u003e \u003cp\u003e\u003ci\u003eAngewandte Chemie International Edition \u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\"...industrial chemists, college and university teachers, and students will find the book very useful and a valuable addition to their bookshelves...useful for chemical engineers as well as engineers in the chemical and petrochemical industries.\"\u003c\/p\u003e \u003cp\u003e\u003ci\u003ePetroleum Science and Technology \u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\"...valuable to a wide range of readers....\"\u003c\/p\u003e \u003cp\u003e\u003ci\u003eEnergy Sources \u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\"...useful to anyone needing information about the important field of hydrocarbons, and the updates in this edition's references are especially valuable...highly recommended.\"\u003c\/p\u003e \u003cp\u003e\u003ci\u003eChoice \u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\"...will be a continuing first-source of vital information for this core component of contemporary organic chemistry.\"\u003c\/p\u003e \u003cp\u003e\u003ci\u003eJournal of the American Chemical Society \u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eBuilding on the legacy of its successful predecessor, this revision of \u003ci\u003eHydrocarbon Chemistry\u003c\/i\u003e begins by discussing the general aspects of hydrocarbons, the separation of hydrocarbons from natural sources, and the synthesis from C1 precursors with recent developments for possible future applications. Each successive chapter deals with a specific type of hydrocarbon transformation.\u003c\/p\u003e \u003cp\u003eSince the publication of the 2nd edition, the field of hydrocarbon chemistry has rapidly grown and expanded both in its scientific scope and significances and provides the most promising approach to replace oil and, eventually, all fossil fuel. It is also able to render the use of still existing substantial fossil fuels environmentally adaptable by capturing and recycling CO2 and recycling it through material to new fuels and chemical raw material – developments that lead to this third edition.\u003c\/p\u003e","brand":"Wiley","offers":[{"title":"Default Title","offer_id":47989392933093,"sku":"NP9781119390510","price":504.95,"currency_code":"USD","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1842\/7735\/files\/9781119390510.jpg?v=1761783935","url":"https:\/\/k12savings.com\/es\/products\/hydrocarbon-chemistry-2-volume-set-isbn-9781119390510","provider":"K12savings","version":"1.0","type":"link"}