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3- Ethyl-2-methylpentane

The correct name is 3-ethyl-2-methylpentane (disub stituted chain) rather than 3 isopropylpentane (monosubstituted chain)... [Pg.97]

DIMETHYLHEXANE 3-ETHYLHEXANE 3-ETHYL-2-METHYLPENTANE 3-METHYL-3-ETHYLPENTANE... [Pg.98]

B-8. Which of the following substances is not an isomer of 3-ethyl-2-methylpentane ... [Pg.45]

Many authors elucidated functionalization of polymers containing reactive oxirane moieties. Epoxidized NR, BR, IR and/or the respective model hydrocarbons, poly (butadiene-co-isoprene, various epoxy resins, poly (2,3-epoxypro-pyl methacrylate) and its copolymers or grafted systems were mostly exploited. Stabilizers based on epoxidized unsaturated rubbers are of the top interest. The mechanism of the functionalization process was studied in details by means of 3,4-epoxy-4-methylheptane and 1,2-epoxy-3-ethyl-2-methylpentane as model compounds [289]. The ring opening of the asymmetric oxirane is regiospecific. Aliphatic primary amines attack the least substituted carbon atom and can be involved in crosslink formation. Aromatic primary and secondary amines are less reactive than aliphatic ones because of their lower basicity the attack on the least substituted carbon atom is however preferred too. [Pg.136]


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See also in sourсe #XX -- [ Pg.44 ]

See also in sourсe #XX -- [ Pg.1018 ]




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