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Trimethyl amine methyl iodide reaction

Calculate activation energies for Sn2 reactions of ammonia and trimethylamine with methyl iodide via transition states ammonia+methyl iodide and trimethyl-amine+methyl iodide, respectively. Is attack by ammonia or trimethylamine more facile Rationalize your observation by comparing electrostatic potential maps for the two transition states. Which transition state requires more charge separation Is this also the higher-energy transition state ... [Pg.204]

A thio-substituted, quaternary ammonium salt can be synthesized by the Michael addition of an alkyl thiol to acrylamide in the presence of benzyl trimethyl ammonium hydroxide as a catalyst [793-795]. The reaction leads to the crystallization of the adducts in essentially quantitative yield. Reduction of the amides by lithium aluminum hydride in tetrahydrofuran solution produces the desired amines, which are converted to desired halide by reaction of the methyl iodide with the amines. The inhibitor is useful in controlling corrosion such as that caused by CO2 and H2S. [Pg.92]


See other pages where Trimethyl amine methyl iodide reaction is mentioned: [Pg.271]    [Pg.386]    [Pg.585]    [Pg.209]    [Pg.332]    [Pg.472]    [Pg.1302]    [Pg.1989]    [Pg.107]    [Pg.20]    [Pg.130]    [Pg.3218]    [Pg.207]    [Pg.3217]    [Pg.63]   
See also in sourсe #XX -- [ Pg.202 ]




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Amines methylated

Iodide reaction

Methyl amine

Methyl amine reactions

Methyl iodide

Methyl iodide, reactions

Trimethyl-amine

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