if you could show how to do this radical mechanism that would be helpful
if you could show how to do this radical mechanism that would be helpful
fi you could answer this question with a radical mechanism that would be helpful Bu3SnH, AlBN heat S-Ph
If you could show mechanism that would be helpful 4. Predict products for the following reactions. Indicate stereochemistry where available. NC high temperature retro Diels-Alder 5. Draw the MAJOR potential bicyclic Diels-Alder product for the reaction below.
Write a mechanism for the following radical halogenation reaction. Also, do you happen to know how i would enter this into the online system?? Problem 10.18 Write a mechanism for the following radical halogenation reaction. hv Draw the initiation step of the mechanism. Include a one pairs, formal charges and radicals in the mechanism. Edit
if someone could show me how to do these problems it would be very helpful. Orate the major products) or pronde the reagents for each reachan below lise bold and dashed wedges to show the proper stereochemistry where necessary Write both the O- and p- products where necessary (3pts each answer). Br (A) NILE NBS Kinenc Product Thermodynamio Product CHCH3 X CH₂ CH3 Na liquid Nitz (E) HO CH-C-CHE 0 etts CHg thay chci AlC3 hsou (G) NO₂ Chzical AlCl3...
Could someone show me how to do this: Predict the major product(s) in the radical-chain monochlorination of 2, 3-dimethylpentane.
how do you solve this out step by step if you could include some helpful explanations please. I totally forgot how to do this!( explain the quickest method for doing this please if you can!) 0= 4x+ 4.66X16*- 3.728x16-3 4x + 4.66 * xlo
a. Show how a tosylate ester could be helpful in converting 1-propanol into ethyl propyl ether. b. Show how a tosylate ester could be helpful in converting 2-butanol into 2-butanamine.
Can anyone show how to find the major product(s)? If you could include mechanism and stereochemistry where applicable I would greatly appreciate it.
I had a question regarding free radical substitution reaction (initiation, propagation, and termination). How do you form CH2 = CH2 ??? I believe this is formed in the termination step but how is it? Could you please show the steps so I can understand and learn. I will rate! Please answer ASAP. Thank You
f. From your knowledge of the radical addition mechanism, what product would you expect from the treatment of 1,3-butadiene with HBr in peroxide containing ether. Support your answer by showing the mechanism for the reaction and the role played by the peroxide. (6 pts)