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1 -Bromo-2-methylcyclohexane

Dehydrohalogenation of 1-bromo-1-methylcyclohexane with a strong base (NaOH or potassium tert-butoxide) would also provide the desired alkene. This reaction, however, would be complicated by the formation of methylcyclohexene as the major product. [Pg.122]

C7H1202 methyl trans-3-methyl-2-pentenoate 17447-01-7 424.15 36.647 1,2 11573 C7H13Br 1 -bromo-1 -methylcyclohexane 931-77-1 431.15 37.310 1,2... [Pg.457]

Compound A reacts with one equivalent of H2 in the presence of a catalyst to give methylcyclohexane. Compound A can be formed upon treatment of 1-bromo-1-methylcyclohexane with sodium methoxide. What is the structure of compound A ... [Pg.450]

Methylcyclohexanol, on (reatment with HBr, gives 1-bromo- 1-methylcyclohexane. Explain by a... [Pg.332]

See other pages where 1 -Bromo-2-methylcyclohexane is mentioned: [Pg.133]    [Pg.35]    [Pg.267]    [Pg.272]    [Pg.481]    [Pg.192]    [Pg.192]    [Pg.193]    [Pg.210]    [Pg.1382]    [Pg.133]    [Pg.260]    [Pg.755]    [Pg.227]    [Pg.230]    [Pg.240]    [Pg.198]    [Pg.182]    [Pg.182]    [Pg.925]   
See also in sourсe #XX -- [ Pg.264 , Pg.266 ]



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1-Bromo-l-methylcyclohexane

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