Safety of 1-Iodo-2-methylbutane. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 1-Iodo-2-methylbutane, is researched, Molecular C5H11I, CAS is 616-14-8, about Kinetics, products and mechanism of O(3P) atom reactions with alkyl iodides. Author is Barnes, Ian.
Alkyl halides are an important source of halogens in the atm. In the case of alkyl iodides, relative kinetic studies of their OH reactions in photoreactors are complicated by fast reactions with the O(3P) atoms generated by the photochem. OH radical sources. In the present study, the relative kinetic technique was applied in large and small photoreactors to measure rate coefficients for the reaction of O(3P) atoms with a series of alkyl iodides at room temperature and atm. pressure. The products formed in N2 were also investigated. Alkenes and HOI are the major products of the reactions and the alkene was quantified for the majority of the alkyl iodides studied.
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Reference:
Thiomorpholine – Wikipedia,
Thiomorpholine | C4H9NS – PubChem