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Terminal alkene

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of the molecule. The red symbols show the common nomenclature labeling of the main chain atoms. The double bond of an alpha olefin is between the #1 and #2 (IUPAC) or α and β (common) carbon atoms.
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Griesbaum, Karl; Behr, Arno; Biedenkapp, Dieter; Voges, Heinz-Werner; Garbe, Dorothea; Paetz, Christian; Collin, Gerd; Mayer, Dieter; Höke, Hartmut (2000). "Hydrocarbons".
410:. Long chain alpha-olefins are also oligomerized to give medium molecular weight oils that serve as lubricants. Alkylation of benzene with alpha-olefins followed by ring- 130:
number are significantly different from the properties of linear alpha-olefins and those with branches on the fourth carbon number and further from the start of the chain.
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position. This location of a double bond enhances the reactivity of the compound and makes it useful for a number of applications.
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A variety of methods are employed for production of alpha-olefins. One class of methods starts with ethylene which is either
485: 126:(or normal). The chemical properties of branched alpha-olefins with a branch at either the second (vinylidene) or the third 418:(LABS) which are biodegradable detergents. Competing often with these petroleum-derived products are derivatives of 521: 415: 17: 166: 383:(paraffin conversion to olefins), linear alkanes are dehydrogenated over a platinum-based catalyst. 177:. A whole other approach to alpha-olefins, especially long chain derivatives, involves cracking of 103: 8: 123: 517: 481: 442: 158: 52: 543: 509: 403: 80: 72: 107: 44: 537: 513: 423: 369:{\displaystyle {\ce {R-CH2-CH2-CH2-CH2-R' -> R-CH=CH2 + CH2=CH-R' + H2}}} 438: 458: 427: 411: 399: 391:
Alpha-olefins are valued building blocks for other industrial chemicals.
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Low molecular weight alpha-olefins (butenes, hexenes, etc.) are used as
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A major portion of medium or long chain derivatives are converted to
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or oligomerized. These conversions are respectively effected by the
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which gives a range of alpha-olefins. The former is based on
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Hydrocarbon compounds with a C=C bond at the alpha carbon
173:-based catalysts, and the latter relies on nickel-based 190: 402:. A common first step in making such products is 368: 535: 505:Ullmann's Encyclopedia of Industrial Chemistry 406:followed by hydrogenation of the resulting 145:. An example of a branched alpha-olefin is 497: 495: 493: 29: 478:Petrochemicals in Nontechnical Language 14: 536: 490: 118:There are two types of alpha-olefins, 133:Examples of linear alpha-olefins are 24: 165:process, giving 1-butene, and the 25: 555: 113: 386: 79:(also known as olefins) with a 471: 437:, which are incorporated into 416:linear alkylbenzene sulfonates 280: 43:numbering of the atoms in the 13: 1: 464: 152: 98:, distinguished by having a 7: 452: 167:Shell higher olefin process 37:, a typical alpha-olefin. 10: 560: 39:The blue numbers show the 441:. Some are subjected to 514:10.1002/14356007.a13_227 508:. Weinheim: Wiley-VCH. 370: 48: 371: 33: 188: 364: 327: 311: 266: 248: 230: 212: 366: 352: 315: 299: 254: 236: 218: 200: 71:) are a family of 49: 486:978-0-87814-798-4 443:olefin metathesis 355: 344: 335: 318: 302: 293: 285: 275: 257: 239: 221: 203: 194: 102:at the primary, 73:organic compounds 53:organic chemistry 16:(Redirected from 551: 528: 527: 499: 488: 475: 404:hydroformylation 375: 373: 372: 367: 365: 363: 360: 353: 348: 342: 340: 333: 332: 326: 323: 316: 310: 307: 300: 298: 291: 290: 283: 279: 273: 271: 265: 262: 255: 253: 247: 244: 237: 235: 229: 226: 219: 217: 211: 208: 201: 199: 192: 97: 81:chemical formula 57:terminal alkenes 21: 559: 558: 554: 553: 552: 550: 549: 548: 534: 533: 532: 531: 524: 500: 491: 476: 472: 467: 455: 389: 361: 356: 341: 336: 328: 324: 319: 308: 303: 294: 286: 272: 267: 263: 258: 249: 245: 240: 231: 227: 222: 213: 209: 204: 195: 191: 189: 186: 185: 155: 116: 96: 89: 83: 38: 28: 23: 22: 15: 12: 11: 5: 557: 547: 546: 530: 529: 522: 489: 469: 468: 466: 463: 462: 461: 454: 451: 445:as a route to 424:fatty alcohols 388: 385: 377: 376: 359: 351: 347: 339: 331: 322: 314: 306: 297: 289: 282: 278: 270: 261: 252: 243: 234: 225: 216: 207: 198: 154: 151: 115: 114:Classification 112: 91: 85: 45:backbone chain 26: 9: 6: 4: 3: 2: 556: 545: 542: 541: 539: 525: 519: 515: 511: 507: 506: 498: 496: 494: 487: 483: 479: 474: 470: 460: 457: 456: 450: 448: 444: 440: 436: 431: 429: 425: 421: 417: 413: 409: 405: 401: 397: 392: 384: 382: 381:PACOL process 357: 349: 345: 337: 329: 320: 312: 304: 295: 287: 276: 268: 259: 250: 241: 232: 223: 214: 205: 196: 184: 183: 182: 180: 176: 172: 168: 164: 160: 150: 148: 144: 140: 136: 131: 129: 125: 121: 111: 109: 105: 101: 95: 88: 82: 78: 74: 70: 66: 62: 61:alpha-olefins 58: 54: 46: 42: 36: 32: 19: 18:Alpha-olefins 503: 477: 473: 439:polyethylene 432: 428:fatty amines 400:plasticizers 393: 390: 387:Applications 378: 156: 132: 117: 93: 86: 68: 64: 60: 56: 50: 459:Vinyl group 420:fatty acids 412:sulfonation 147:isobutylene 100:double bond 523:3527306730 465:References 435:comonomers 422:, such as 396:detergents 163:alphabutol 153:Production 75:which are 447:propylene 408:aldehydes 338:− 288:− 281:⟶ 269:− 251:− 233:− 215:− 197:− 175:catalysts 159:dimerized 143:dec-1-ene 139:but-1-ene 104:alpha (α) 69:1-alkenes 65:α-olefins 35:Hex-1-ene 538:Category 453:See also 346:′ 277:′ 171:titanium 120:branched 544:Alkenes 379:In the 135:propene 77:alkenes 520:  484:  414:gives 128:carbon 124:linear 179:waxes 106:, or 67:, or 41:IUPAC 518:ISBN 482:ISBN 426:and 398:and 141:and 122:and 510:doi 51:In 540:: 516:. 492:^ 449:. 430:. 334:CH 317:CH 301:CH 292:CH 256:CH 238:CH 220:CH 202:CH 181:: 149:. 137:, 108:1- 63:, 55:, 526:. 512:: 358:2 354:H 350:+ 343:R 330:= 321:2 313:+ 305:2 296:= 284:R 274:R 260:2 242:2 224:2 206:2 193:R 94:x 92:2 90:H 87:x 84:C 59:( 20:)

Index

Alpha-olefins

Hex-1-ene
IUPAC
backbone chain
organic chemistry
organic compounds
alkenes
chemical formula
double bond
alpha (α)
1-
branched
linear
carbon
propene
but-1-ene
dec-1-ene
isobutylene
dimerized
alphabutol
Shell higher olefin process
titanium
catalysts
waxes
PACOL process
detergents
plasticizers
hydroformylation
aldehydes

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