if propane is reacted w/ Cl2 in the presence of UV light what products form and in what percentages? A) propyl chloride 100% B) 42% propyl chloride and 58% isopropyl chloride C) 75% propyl chloride and 25% isopropyl chloride D) 90% propyl chloride and 10% isopropyl chloride
not allowed to use a calculator on my upcoming exam so was wondering the best way to reason this one out by hand Please do not comment unless you are actually familiar with the subject and are making a serious attempt at the problem.
Radical intermediates
my first instinct was D b/c the propyl radical is more stable but apparently that's not it
the more the hyperconjugation the more the stability of your radical
|dw:1564199910099:dw| stability order
the left one is more stable because it has more \(\alpha\) hydrogens
ah nvm I had propyl/isopropyl mixed up >> thank you
the mechanisms involving radicals are fast and they don't allow the radicals to rearrange to their most stable position, they just react instantaneously
good to know thank you
np
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