For the first question, I was going to say that structure C would have the lowes
ID: 981927 • Letter: F
Question
For the first question, I was going to say that structure C would have the lowest yield because of the close proximity to the preexisting Chloride atom. But is there any other explination that could apply to this?And I have no idea what to put down for the 2nd question.
w the 4 dichlorinated products of the radical reaction shown. Based on your results for this experiment predict the product that will have the lowest yield for t Justify your prediction. I. Draw the 4 dichlorinated products of the radical reaction shown. Base he reaction below he lowest yield for the reaction below cl Cl SOCI, AIBN cl In the balanced reaction of sulfuryl chloride and 1-chlorobutane the mole ratio of reactants is 1:1. In lab you used approximately 2X as many moles of chlorobutane as sulfuryl chloride. Offer an explanation for the molar ratio of these reactants in your experiment 2.
Explanation / Answer
question 1
your option is correct but your explanation is wrong
in chlorination reaction one of the step is chlorine radical will pick the hydrogen radical right?
in that step Chlorine will pick the hydrogen where the no of hydrogens more
if you observe your starting material there are three type of H are there
one is Hydrogens which is attached to CH3 groups. 2 CH3 groups are there so 6 H
Hydrogens attached to CH2 so 2 H
Hydrogens attached to CH which is only one H
Cl radical will have less selectivity compare to Br rradical so it will randamly pick the Hydrogen radical
so wherever no of hydrogens are more there it will pick the Hydrogen radical and will get corresponding dichloro product
accordingly there is only one CH is there so picking of this hydrogen as a radical is very less so this is the least dichloro product.
question 2
because one mole of SoCl2 will produce 2 moles of Cl radicals because it is SOCl2
so obviously one mole of SoCl2 required 2 moles of chloro butane