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Alicyclic compound

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group is always shown outside the ring structure, take for instance the exocyclic double bond of the former molecule.
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Christmann, M (2010). "Otto Wallach: Founder of Terpene Chemistry and Nobel Laureate 1910".
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The mode of ring-closing in the formation of many alicyclic compounds can be predicted by
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The placement of double bonds in many alicyclic compounds can be predicted with
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have two or more rings that are connected through only one carbon atom.
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are a prominent class of compounds with exocyclic double bonds.
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Organic molecule with one or more non-aromatic all-carbon rings
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The simplest alicyclic compounds are the monocyclic
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character. Alicyclic compounds may have one or more
368: 306: 182:is an alicyclic compound with a double bond. 334: 235: 174: 36: 337:Angewandte Chemie International Edition 14: 369: 214:, and so on. Bicyclic alkenes include 157:, a German chemist, received the 1910 161:for his work on alicyclic compounds. 225:Two more examples are shown below, 44:is the smallest alicyclic compound. 24: 283:Compendium of Chemical Terminology 25: 388: 56:contains one or more all-carbon 164: 328: 300: 271: 13: 1: 264: 7: 240:Left: exocyclic double bond 10: 393: 242:Right: regular double bond 168: 29: 159:Nobel Prize in Chemistry 62:saturated or unsaturated 296:10.1351/goldbook.A00216 349:10.1002/anie.201003155 243: 183: 45: 239: 178: 169:Further information: 40: 322:10.1039/JR9320001582 227:methylenecyclohexane 60:which may be either 288:Alicyclic compounds 231:1-methylcyclohexene 244: 184: 64:, but do not have 54:alicyclic compound 46: 377:Organic compounds 343:(50): 9580–9586. 50:organic chemistry 16:(Redirected from 384: 361: 360: 332: 326: 325: 304: 298: 275: 229:on the left and 126:alkanes include 110:alkanes include 21: 392: 391: 387: 386: 385: 383: 382: 381: 367: 366: 365: 364: 333: 329: 308:Leopold Ruzicka 305: 301: 276: 272: 267: 241: 173: 167: 149:Baldwin's rules 142:Spiro compounds 112:bicycloundecane 35: 28: 23: 22: 15: 12: 11: 5: 390: 380: 379: 363: 362: 327: 299: 269: 268: 266: 263: 233:on the right: 166: 163: 26: 9: 6: 4: 3: 2: 389: 378: 375: 374: 372: 358: 354: 350: 346: 342: 338: 331: 323: 319: 315: 314: 313:J. Chem. Soc. 309: 303: 297: 293: 289: 285: 284: 279: 274: 270: 262: 260: 255: 253: 249: 238: 234: 232: 228: 223: 221: 220:norbornadiene 217: 213: 209: 205: 201: 197: 193: 189: 181: 177: 172: 162: 160: 156: 152: 150: 145: 143: 139: 137: 133: 129: 125: 121: 117: 113: 109: 106:, and so on. 105: 101: 97: 93: 89: 85: 81: 76: 74: 71: 67: 63: 59: 55: 51: 43: 39: 33: 19: 340: 336: 330: 311: 302: 281: 273: 259:Bredt's rule 256: 247: 245: 224: 208:cycloheptene 200:cyclopentene 192:cyclopropene 188:cycloalkenes 185: 165:Cycloalkenes 155:Otto Wallach 153: 146: 140: 136:tetrahedrane 100:cycloheptane 92:cyclopentane 84:cyclopropane 80:cycloalkanes 77: 53: 47: 42:Cyclopropane 252:Isotoluenes 212:cyclooctene 204:cyclohexene 196:cyclobutene 186:Monocyclic 180:Cyclohexene 171:Cycloalkene 104:cyclooctane 96:cyclohexane 88:cyclobutane 73:side chains 32:Aromaticity 265:References 216:norbornene 124:Polycyclic 75:attached. 248:exocyclic 132:basketane 70:aliphatic 18:Alicyclic 371:Category 357:21110354 316:: 1582. 108:Bicyclic 66:aromatic 120:housane 116:decalin 355:  134:, and 128:cubane 118:, and 278:IUPAC 58:rings 52:, an 353:PMID 218:and 190:are 345:doi 318:doi 292:doi 290:". 246:An 48:In 373:: 351:. 341:49 339:. 280:, 261:. 222:. 210:, 206:, 202:, 198:, 194:, 151:. 138:. 130:, 122:. 114:, 102:, 98:, 94:, 90:, 86:, 82:: 359:. 347:: 324:. 320:: 294:: 34:. 20:)

Index

Alicyclic
Aromaticity

Cyclopropane
organic chemistry
rings
saturated or unsaturated
aromatic
aliphatic
side chains
cycloalkanes
cyclopropane
cyclobutane
cyclopentane
cyclohexane
cycloheptane
cyclooctane
Bicyclic
bicycloundecane
decalin
housane
Polycyclic
cubane
basketane
tetrahedrane
Spiro compounds
Baldwin's rules
Otto Wallach
Nobel Prize in Chemistry
Cycloalkene

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