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2-Propenal 2- methyl

ACETATE], 32 1 Propene, 2-methyl-, 35 2-Propen-l-ol, 2-bromo 3-phenyl-, acetate, 35... [Pg.143]

Methyl-1-phenyl-propen — (2-Methyl-propyl)-benzol 97% d.Th. [Pg.69]

Propene 2-Methyl-l-nitro-3.3,3-triflttoro- ElOa, 349f. (COOH -> CF.,)... [Pg.601]

The modern view of HX addition is that H+ is transferred from HX to the alkene to give a carbocation. The major product is the one derived from the more stable carbocation. Compare the energies of 1-propyl and 2-propyl cations (protonated propene), 2-methyl-1-propyl and 2-methyl-2-propyl cations (protonated 2-methylpropene), and 2-methyl-2-butyl and 3-methyl-2-butyl cations (protonated 2-methyl-2-butene). Identify the more stable cation in each pair. Is the product derived from this cation the same product predicted by Markovnikov s rule Is the more stable carbocation also the one for which the positive charge is more delocalized Compare atomic charges and electrostatic potential maps for one or more pairs of carbocations. [Pg.63]

The presence of a 3-methyl group in 53 changes the reaction course. When the oxidant Se02 is used in more than twofold excess relative to 3-methyl-2//-tellurachromene, bis[2-(3 -propene-2 -methyl-1 -al)phenyl]-ditelluride 56a is formed in 60% yield. When a smaller relative amount of Se02 is used in this reaction, aldehyde 56a is formed along with the product of selenium insertion into the Te—Te bond, 58 (in 15% yield [83JOM(258)163]. [Pg.27]

Isobutene Propene, 2-methyl- (8) 1-Propene, 2-methyl- (9) (115-11-7) Phosphorus oxychloride [POCl3] Phosphoryl chloride (8, 9) (10025-87-... [Pg.150]

Oxiran 2-Methyl-3-(4-methyl phenyl)-2-trimethyl-silyl- E19d, 881 (H - Li/ + R-CHO) Propen 2-Methyl-l-phenyl-1-trimethylsilyloxy- E1S/1, 441 (Keton + R3Si —O —S02 —R) Silan Dimethyl-pentanoyl-phenyl-E19d, 570 (Acylierung) Spiro[4.4]nona-2,6-dien 6-Methyl-l -oxo-2(bzw. 3)-trimethylsiiyl-E19c, 221 (3-En-CO-Cl +... [Pg.1181]

SYNS ACROLEIN, 2-METHYL- ISOBUTENAL METHACRALDEHYDE (DOT) METHACROLEIN METHACRYLIC ALDEHYDE METHAKRYLALDEHYD a-METHYL. CROLEIN 2-METHYLACROLEIN O METHYLACRYLALDEHYDE 2-METHYLPROPENAL (CZECH) NSC-8260 2-PROPENAL, 2-METHYL-... [Pg.895]

Propene, 2-methyl (isobutylene) Propenoic acid nitrile (acrylonitrile)... [Pg.483]

C.32) (C.32) 2-Propenal, 2-methyl-, 2-methylacrylaldehyde, 2-methylprop-2-enal, isobutenal, 2-methylenepropanal, methacrylaldehyde, a-methylacrolein, methacrolein 178-85-3]... [Pg.121]

Hydrogen atom abstraction from —CH3 groups accounts generally for <5% of the overall OH reaction of ethene and the methyl-substituted ethenes (propene, 2-methyl propene, the 2-butenes, 2-methyl-2-butene, and 2,3-dimethyl-2-butene). For alkenes with alkyl side chains, perhaps up to 10% of the OH reaction proceeds by H-atom abstraction, but we will neglect that path here. [Pg.247]


See other pages where 2-Propenal 2- methyl is mentioned: [Pg.36]    [Pg.108]    [Pg.136]    [Pg.309]    [Pg.48]    [Pg.19]    [Pg.310]    [Pg.191]    [Pg.160]    [Pg.161]    [Pg.163]    [Pg.168]    [Pg.407]    [Pg.430]    [Pg.536]    [Pg.751]    [Pg.828]    [Pg.884]    [Pg.1854]    [Pg.324]    [Pg.347]    [Pg.84]    [Pg.94]    [Pg.343]    [Pg.31]    [Pg.245]    [Pg.245]    [Pg.245]    [Pg.1725]    [Pg.1725]    [Pg.1725]   
See also in sourсe #XX -- [ Pg.174 ]

See also in sourсe #XX -- [ Pg.174 ]




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2-Methyl-2-propen

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