Yes, it can be converted thermally or photochemically by dehydrogenation using iridium complexes as catalysts.
when one or more hydrogens of alkanes are displaced by other atoms or group of atoms then reactions are the substitution reactions....
yes
Any number of chemical moieties could react with alkanes to produce new compounds in a substitution reaction. For example, hydrohalic acids (HCl, HBr, HI) could react with an alkane to produce a haloalkane. Here, the halogen atom would replace one of the hydrogen atoms in the alkane. (HCl + ethane --> chloroethane) (HBr + propane --> bromopropane) This also works with other reactive species, such as: - nitric acid + alkane --> nitroalkane
Addition -Harvard unervisty
due to saturated and single bonded.
Iodine is a very huge molecule and low electronegative that's why it always gives very slow or reversible reactions.
Alkane molecules are nonpolar.
Gary Craig Hanson has written: 'Mechanistic study of some internal substitution reactions and a substitution at sulfenyl sulfur' -- subject(s): Substitution reactions
Any number of chemical moieties could react with alkanes to produce new compounds in a substitution reaction. For example, hydrohalic acids (HCl, HBr, HI) could react with an alkane to produce a haloalkane. Here, the halogen atom would replace one of the hydrogen atoms in the alkane. (HCl + ethane --> chloroethane) (HBr + propane --> bromopropane) This also works with other reactive species, such as: - nitric acid + alkane --> nitroalkane
Keith U. Ingold has written: 'Free-radical substitution reactions' -- subject(s): Substitution reactions, Radicals (Chemistry)
Addition -Harvard unervisty
aniline would go through an electrophilic substitution, it is a weak base
due to saturated and single bonded.
because, phenol it self neucleophilic group.
2-nitro toluene may under go electrophilic substitution reactions as Nitration, Halogenation at 4th position.
John James Hoffman has written: 'The theory of substitution in benzene derivatives' -- subject(s): Nitrous acid, Phenylether, Substitution reactions
Iodine is a very huge molecule and low electronegative that's why it always gives very slow or reversible reactions.
in sn1 reactions polar solvents are used.why b coz, polar solvent stabilise the intermediate which is formed in the reaction.but in sn2 reactions non polar solvents are used.in this reaction intermediate is not formed.
alkane