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6. (6pts) For each of the radicals below, please exaplin what contributes to the stability of...
6. (6pts) For each of the radicals below, please exaplin what contributes to the stability of the radical and circle the more stable radical. 7. (5pts) of the reducing agents that we discussed during lecture, what would you use to reduce an amide?
6. (6pts) For each of the radicals below, please exaplin what contributes to the stability of the radical and circle the more stable radical.
6. (6pts) For each of the radicals below, please exaplin what contributes to the stability of the radical and circle the more stable radical.
7. (5pts) Of the reducing agents that we discussed during lecture, what would you use to reduce an amide?
7. (5pts) of the reducing agents that we discussed during lecture, what would you use to reduce an amide? 8.(12 pts) Draw a detailed stepwise mechanism for the following reaction. Must include ALL steps. 1) Br, hv 2) Mg(s) 3) OH 요 4) H30+
help with this worksheet please! 1. Determine the radical stability with 1 the most stable and 4 the least stable 2. What is the major product of 2-methylpropane mono-chlorination? Cl2 light 3. Calclate AH for chlorination of methane (DHe for CHa-H is 440 kJ/mol; DH° for Cl-Cl is 243 kJ/mol; DH° for CH3-Cl is 432 kJ/mol; and DH° for H-Cl is 353 kJ/mol 4. Draw structure of the most stable radical formed by hydrogen radical abstraction from 3- methylcyclohexene 5....
11. Which of the following best explains why the synthetic route shown below would be unsuccessful? 2) NaNH2 3) (CHs)hCBr A) The alkynide anion is not a strong enough nucleophile to react with 1-bromopropane in step 1 m amide is not a strong enough base to deprotonate the terminal alkyne in step anion formed by reaction with sodium amide will facilitate an E2 (rather C) The alkynide than SN2) reaction with t-butyl bromide. 5oth substtution reactions will occur on the...
CHM 2440 (FA 2019) 6. Complete the mechanism of addition of HCl to propene below. Please use curved arrows to indicate the electron(s) movements. (1 pt, 0.5 pr each) Step 1. Note that the most stable carbocation is formed here. Step 2. 7. Which alkene below reacts most rapidly with HBr to give an alkyl bromide? Circle it. (0.25 pt) Hint: The alkene that can generate the most stable carbocation will react the fastest.
Help with questions 2, F on question 8a, and question 8b please. UUUU CHEM 2030, Sections 3.5-3.9 Reactions and Mechanisms, Introduction College Tip: Please read and take notes on the chapter before coming to class. It reduces overall anxiety and other feelings of discomfort. Additionally, it increases feelings of understanding and helps you ask more 'in-depth' questions. Instructions. Please see previous handouts for repetitive instructions. Oa. Memorize all boldface words in the chapter and be able to use them in...
Please tell me if i have part (a) correct or not? and answer part (b) for me please with clear hand wrriten please. Question 8) A) Below is a reaction scheme you performed in lab to reduce 4-+-butylcyclohexanone to the corresponding cis and trans secondary alcohol isomers. In lab you used NaBH4 to reduce the ketone, but state whether it is also possible to use LiAIH4. If so, why did we choose NaBHs instead of LiAIH? OH NaBH4 MeOH 个个and...