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Tert-Butyl bromide with hydrogen chloride

The major difference between the two mechanisms is the second step The second step m the reaction of tert butyl alcohol with hydrogen chloride is the ummolecular dis sociation of tert butyloxonium ion to tert butyl cation and water Heptyloxonium ion however instead of dissociating to an unstable primary carbocation reacts differently It IS attacked by bromide ion which acts as a nucleophile We can represent the transition state for this step as... [Pg.164]

See other pages where Tert-Butyl bromide with hydrogen chloride is mentioned: [Pg.86] [Pg.51] [Pg.111] [Pg.82] [Pg.163] [Pg.36] [Pg.120] [Pg.314] [Pg.700] [Pg.274]

See also in sourсe #XX -- [ Pg.149 , Pg.150 , Pg.151 , Pg.152 ]

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1- Butyl-3- chlorid

Bromide,tert

Bromides hydrogenation

Butyl bromide

Butyl bromide chloride

Butyl chloride

Butylated butyl bromide

Butylated butyl chloride

Hydrogen bromid

Hydrogen bromide

Tert chloride

Tert-butyl bromide

Tert.-Butyl chloride

With Hydrogen Bromide