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1-butene, 2,3,3-trimethyl

Trimethyl- 1-butene r/.v.r/.v-1.3.5-Trim ethyl cyclohexane Trimethylene oxide... [Pg.880]

TRIMETHYL-1-BUTENE 34.3198 -2.7439E+03 -9.4453E+00 4.8805E-11 3.4012E... [Pg.41]

Trimethyl-1 -butene gives only (CH3)3CC=CH2 1-Octene gives a mixture of... [Pg.1223]

NAME 2, 3, 3-Trimethyl-1-butene STRUCTURAL FORMULA CH,C C = CH, 31 i c ch3ch3... [Pg.282]

C7H14 2,3,3-trimethyl-1 -butene 594-56-9 1.095E-h10 74.960 14083 C8H11N o-ethylaniline 578-54-1 9.810E-K09 77.760... [Pg.654]

PROBLEM 10.5 The two alkenes 2,3,3-trimethyl-1-butene and 1-octene were each subjected to allylic halogenation with A/-bromosuccinimide. One of these alkenes yielded a single allylic bromide, whereas the other gave a mixture of two constitutionally isomeric allylic bromides. Match the chemical behavior to the correct alkene and give the structure of the allylic bromide(s) formed from each. [Pg.372]

See other pages where 1-butene, 2,3,3-trimethyl is mentioned: [Pg.396]    [Pg.398]    [Pg.579]    [Pg.611]    [Pg.323]    [Pg.372]    [Pg.396]    [Pg.398]    [Pg.1208]    [Pg.950]    [Pg.848]    [Pg.15]    [Pg.68]    [Pg.96]    [Pg.123]    [Pg.161]    [Pg.187]    [Pg.321]    [Pg.403]    [Pg.377]    [Pg.380]    [Pg.94]    [Pg.232]    [Pg.232]    [Pg.119]    [Pg.130]    [Pg.960]    [Pg.602]    [Pg.3]    [Pg.613]    [Pg.411]    [Pg.372]    [Pg.397]    [Pg.408]    [Pg.3]    [Pg.375]    [Pg.381]    [Pg.386]    [Pg.391]    [Pg.402]    [Pg.354]    [Pg.345]    [Pg.386]   


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2.3.3- Trimethyl-l-butene

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