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1.2- Dibromo-3-methylbutane

Isoprene has sometimes been used as a starting matenal in the laboratory synthesis of ter penes In one such synthesis the first step is the electrophilic addition of 2 moles of hydrogen bromide to isoprene to give 1 3 dibromo 3 methylbutane... [Pg.1107]

Methyl iso-Propyl Ketone (13, 68) In 80 per cent yields by hydrolysis of 2,3-dibromo-2-methylbutane with Twitchell s reagent. Colonge, Bull. soc. chim. (5) 3, (1936). [Pg.84]

Probiwn 13.46 Use formaldehyde and 2-butanol to prepare l,2-dibromo-2-methylbutane. ... [Pg.286]

Methyl-l-butene l,2-Dibromo-3-methylbutane 3-Methyl-l-butyne... [Pg.380]

Exercise 27-3 The nmr spectrum of the ferf-butyl protons of 3,3-dibromo-2,2-di-methylbutane is shown as a function of temperature in Figure 27-4. Explain the two peaks observed at—64°. Calculate the approximate mean lifetime of the process that causes the lines to coalesce at —33°. [Pg.1347]

Reactions with dihalomcthanes, 1,3-dibromopropane, 2,3-dibromobutane, 2,3-dibromo-2-methylpentane, 1,2-dibromocyclohexane, and 2-iodo-2-methylbutane did not produce telluronium salts. The halides were converted to alkenes1. [Pg.681]


See other pages where 1.2- Dibromo-3-methylbutane is mentioned: [Pg.373]    [Pg.373]    [Pg.324]    [Pg.41]    [Pg.349]    [Pg.349]    [Pg.369]    [Pg.257]    [Pg.373]    [Pg.1107]    [Pg.373]    [Pg.1107]    [Pg.9]    [Pg.899]    [Pg.326]    [Pg.167]    [Pg.64]    [Pg.326]    [Pg.169]    [Pg.219]    [Pg.220]    [Pg.682]    [Pg.169]    [Pg.1114]    [Pg.133]    [Pg.1262]    [Pg.17]    [Pg.17]    [Pg.17]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.121]    [Pg.121]    [Pg.121]    [Pg.122]    [Pg.122]    [Pg.122]    [Pg.324]    [Pg.324]    [Pg.324]    [Pg.324]    [Pg.324]    [Pg.325]    [Pg.325]    [Pg.325]    [Pg.430]    [Pg.430]   
See also in sourсe #XX -- [ Pg.257 ]




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