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Chloro-2-methylpropane

Chloro 2 methylpropane Isobutyl chloride or 2 methylpropyl chloride 2 Chloro 2 methylpropane tert Butyl chloride or 1 1 dimethylethyl chloride... [Pg.1205]

Problem 16.57 Prepare methyl 2-methylpropanesulfonate from 1-chloro-2-methylpropane. -4... [Pg.363]

C4H2 biacetylene 460-12-8 3.840E-1-09 31.280 3611 C4H9CI 1 -chloro-2-methylpropane 513-36-0 7.960E+09 55.970... [Pg.651]

All of the structures in the left-hand side are the same because all of the positions on the methyl group are identical the compounds are all 1 -chloro-2-methylpropane. [Pg.324]

One of the most striking differences between conjugated dienes and typical alkenes is in their electrophilic addition reactions. To review briefly, the addition of an electrophile to a carbon-carbon double bond is a general reaction of alkenes (Section 6.8). Markovnikov regiochemistry is found because the more stable carbocation is involved as an intermediate. Thus, addition of HCl to 2-methylpropene yields 2-chloro-2-methylpropane rather than 1-chloro-2-methylpropane, and addition of 2 mol equiv of HCl to the noncon-jugated diene 1,4-pentadiene yields 2,4-dichloropentane. [Pg.529]


See other pages where Chloro-2-methylpropane is mentioned: [Pg.177]    [Pg.451]    [Pg.465]    [Pg.499]    [Pg.543]    [Pg.587]    [Pg.1087]    [Pg.1095]    [Pg.1095]    [Pg.192]    [Pg.473]    [Pg.391]    [Pg.734]    [Pg.1356]    [Pg.14]    [Pg.144]    [Pg.28]    [Pg.62]    [Pg.610]    [Pg.769]    [Pg.2029]    [Pg.2365]    [Pg.67]    [Pg.192]    [Pg.28]    [Pg.78]    [Pg.63]    [Pg.233]    [Pg.13]    [Pg.214]    [Pg.423]    [Pg.557]    [Pg.603]    [Pg.162]    [Pg.192]    [Pg.417]   
See also in sourсe #XX -- [ Pg.177 ]




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1 Chloro 2 methylpropane chloride

1- Chloro-2-methylpropane Isobutyl chloride

2 Chloro 2 methylpropane Butyl chloride

2 Methylpropanal

2 Methylpropane

2- Chloro-2-methylpropane substitution

2- Chloro-2-methylpropane, solvolysis

2-Methylpropan

C4H.C1 2-Chloro-2-methylpropane

Solvolysis of 2-chloro-2-methylpropane

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