
Need help with both 3 and 4 please


Need help with both 3 and 4 please 3. The reactions below refer to questions 5-7 and illustrate the reaction steps in t...
Model 3: Reactions of Bromine Radical with Various Alkanes For each reaction below, the most likely products are shown. H H H H Rxn I : Br -H H H H H H H H Br H Rxn IV C- H H CHy сн, H,C нC Rxn V BrH н.с CH -сн Critical Thinking Questions 5. Label the carbon radicals in Model 3 as methyl. primary, secondary, tertiary, allyl or benzyl. a) Which carbon radical in Model 3 is closest...
4. [12 pts] Propose mechanisms for the formation of all 3 products shown in the reaction below: (draw curved arrows, intermediates, and resonance structures if necessary. NO NEED FOR TRANSITION STATES! CH CH CH CH Br Heat CH,CH,OH OCH.CH Mechanism.14 points) Mechanism 2 points) Mechanism.3 14 points) 5. [14 pts] Provide the major products of reacting the alkene shown in the middle of the scheme below with all the reagents independently. Draw the products' structures in the corresponding table below...
Please help with questions 1-5. I have attached the additional
lab information pages for help if you are unclear on anything
please review those.
We were unable to transcribe this imageEAS 97 5. Calculate the theoretical yiel te the theoretical yield of iodinated salicylamide (product) ass Todination reaction. (Show your calculations.) mide (product) assuming a mono- le, your starting material, is shown in Figure 4. ces in the functional group region of the spectrum IR spectrum of salicylamide, your starting...