1. Draw all the products that would have resulted if 2-chlorobutane were used for a radical...
In free radical chlorination of 1-chlorobutane , why dont the products form in equal amounts? In free radical chlorination of 1-chlorobutane what is the major product?
Write out a detailed mechanism (with curved arrows) of the radical chlorination of 1-chlorobutane with Azobisisobutyronitrile (AIBN) as the initiator and sulfuryl chloride. For the mechanisms, make sure to show how to get to the products 1,1-dichlorobutane, 1,2-dichlorobutane, 1,3-dichlorobutane, 1,4-dichlorobutane.
draw all the possible monochlorination products that could possibly be formed upon radical chlorination of 2-methylpentane. Highlight the product you believe would be formed in greatest quantity. **i was able to draw 6, but i feel they may be wrong - 3-chloro-2-methylpentane, 2-chloro-4-methylpentane, 1-chloro-4-methyl, 2,3,3-dimethylchloropentane, 2,2-chloromethylpentane, 2-chloromethylpentane**
Draw all the products resulting from the free radical chlorination of 2,4-dimethyl pentane, and predict the relative product distribution. Assume a ratio of 5.5 : 3.75 : 1.0 for the relative reactivity of tertiary to secondary to primary hydrogens in the free radical chlorination of unsubstituted alkanes. Express final ratio of products as a percent (total should add up to 100).
aDraw all of the monochlorination productsthat you might obtain from the free-radical chlorination of 3-methylpentane. products that you might obtain from the free-radical chlorination of 3-methylpentane . You do not have to consider stereochemistry. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner .Separate gn from the drop-down menu multiple products using the +si
0. Draw and name all the monochlorination pro obtained from radical chlorination of th s, in the names for stereoisomers. (15 pts) e monochlorination products (including all stereoisomers) that might be adical chlorination of the molecule below. Show absolute configuration, Ron CI Light
Using a piece of paper, draw all the possible monochlorination products that could possibly be formed upon radical chlorination of 2-methylpentane. Highlight the product you believe would be formed in greatest quantity.
What is a possible product for the chlorination of butane? a. 1-chlorobutane b. 2-chlorobutane c. 1,2-dichlorobutane d. all of these are possible
Write all the possible monochlorinated products for the radical chlorination of 1-chloro-4- fluorocyclohexane and arrange the products in order of increasing yield (ignore stereo- chemistry)
2. Numerically rank the radical species below in order of increasing stability 3. Draw all relevant resonance structure for each of the radical species shown below. 4. Predict the major product for the radical chlorination reactions shown below. (i)