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Alkanes can be formed via
1. h__ of a__ (e__ a__)
2. c__ longer chain alkane w/ __ catalyst + heat
> bc smaller = u__
hydrogenation, alkene, electrophilic addition, cracking, Al2O3, useful
Forming alkanes:
Hydrogenation of a__
> conditions: __/Ni catalyst + h__
> a__ + H2 → alkane
alkene, Pt, heat, alkene
Reactions of alkanes
1. C__
2. f__-r__ s__ (to make h__)
combustion, free-radical substitution, halogenoalkanes
Alkanes are generally u__ bc s__ d__ in e-n__ between C & _ THUS is n__-p__ (so no dipoles)
unreactive, small diff, negativities, H, non-polar
Reactions of alkanes: combustion
> complete: alkane + O2 → __ + __
> incomplete: alkane + O2 → __ + __
>> this gas is t__ & colourless & N oxides can lead to a__ rain & kill t__/fish
>> c__ converters help: CO + O2 ;; N oxides r__ ;; unburnt HCs oxidised
CO2, H2O, CO, H2O, toxic, acid, trees, catalytic, reduced
Reactions of alkanes: free radical substitution to make halogenoalkanes
> needs __ (sun) ;; H atom substituted by Cl/Br
> not suitable for making s__ halogenoalkanes
UV, specific

Free-radical subst.:
1st step: __
> Cl-Cl bond broken by __ = 2 r__ (h__ fission)
initiation, UV, radicals, homolytic
Free-radical subst.:
2nd step: __
> Free r__ attack unreactive a__ = 1 C-H bond breaks = a__ radical + HX
>> CH3CH3 + Cl• → •CH2CH3 + HCl
> Alkyl radical attacks h__ = h__ + halogen radical
>> •CH2CH3 + Cl-Cl → CH3CH2Cl + Cl•
> repeat
propagation, radicals, alkane, alkyl, halogen, halogenoalkane

Free-radical subst.:
3rd step: __
> 2 free r__ react → _ product
•CH2CH3 + •CH2CH3 → … OR •CH2CH3 + •Cl → … OR •Cl + •Cl → …
termination, radicals, 1