Question 10 ( Show how you would make the target componds on the right from the starting compounds on the left. Show reagents and conditions where appropriate, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanisms. (土) OH
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- a) Using your knowledge of organic reaction mechanisms, explain the formation of EACH product (A,B) in the following reaction. This will require you to write out MULTIPLE mechanisms (i.e. each product comes from a different reaction pathway). Hint: all reaction pathways start from the same intermediate: NaH is a strong base but cannot deprotonate an sp3 C-H bond! OH он 1) NaH (0.5 equiv) Br + 2) H20 A B b) Briefly explain why there is no epoxide (formed via an intramolecular substitution reaction) in the product mixture of the above reaction?Show two reaction schemes to synthesize the following compounds. Pick one reactionscheme and draw the step-by-step reaction mechanism2. The following reactions are reversible. Propose a mechanism for the forward and reverse reactions.
- plz answer both ( including mechanism)Analyze the reaction schemes below and state (with reasons) whether the reaction conditions supplied in each reaction scheme will result in the products shown as MAJOR PRODUCTS. If wrong products are shown, draw the correct products and provide mechanistic details (curly arrows) of how the right (major) products were formed.In each reaction box, place the best reagent and conditions from the list.
- What is the right reagent in the reaction belowPredict the products for the following reactions by showing complete reaction mechanisms. Also, identify the nucleophilic attack, loss of leaving group, proton transfer, rearrangement in the mechanism steps. Show curved arrows in the reaction mechanisms 1- 2- COCH3 NaBH4/H₂O COCH 3 1. LIAIH4 2. H₂OPlease explain the chosen letter. In the sequence of reactions below, A and B are which of the following? o NaCN, (HCl) H3O+ →B (CH3),CO- A- A а. (CН3)2C(ОН)CN, (CH3)2C(ОH)соон b. (CH3)2C(ОН)CN, (CH3)2C (ОН)2 с. (CНз)2C(ОH)CN, (CH3)2CHCOОН d. (CH3)2C(OH)CN, (CH3)2C=O
- What is the correct sequence of steps for the following transformation? Step 1 Step 2 HO (a) HBr, followed by H20 (b) H2 over Lindlar's catalyst, followed by H2O/H,SO4 (c) H2O/H2SO4/H&SO4, followed by HBr (d) H2 over Pd/C, followed by H20 Which structure corresponds to the missing step in the reaction mechanism for the conversion of the alkene/alcohol to the cyclic ether? HC! H20 + H;O OH OH OH (a) (b) (c) (d)Hello, I do not understand this questions and I am stuck. May I get help please?? Question: Draw the curved arrow mechanism for the following reactionHW9 #5