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- 2. The following radical reaction produces 5 unique products. Draw the products AND SHOW YOUR WORK (arrows). CH3 NBS 5 unique products light1. Draw the MAJOR product of the reaction below. 1. NANH, 2. СH,CH, 3. HgSO, H,SO4, H20 HC = CH 2. The following radical reaction produces 5 unique products. Draw the products AND SHOW YOUR WORK (arrows). CH, NBS 5 unique products lightDetermine which mechanism below is the most correct. Be sure to look at whether the most acidic H is reacting, if the direction of the arrows are correct, and if the correct products are formed based on the mechanism. If the correct answer is Option B, then explain why the other options are incorrect? Explain each option that is incorrect individually.
- 3. Draw the mechanism of the following reaction. Include all lone pairs and formal charges. Br NaNH2 (xs), NH3 Brb Use curved arrows to show the mechanism of the step below. If more than one resonance form of the product is possible, show the most stable form. Arrow-pushing Instructions ^^C↔X™ H to HI.... H3CConsider the reaction between 2-methyl-2-butanol and HBr, shown below. но HBr Br Х
- 3. A) Show all the unique mono-halogenated products for the reaction below. Circle the major product. Br₂ light B) Show the formal arrow pushing mechanism for the first and second propagation step which leads to the radical intermediate of the major product. Be sure to draw in the hydrogen which is being abstracted. Draw the products.Determine which mechanism below is the most correct. Be sure to look at whether the most acidic H is reacting, if the direction of the arrows are correct, and if the correct products are formed based on the mechanism. If the correct answer is Option B, then explain why the other options are incorrect?arning Complete the electron-pushing mechanism for the formation of the major product in the given reaction by adding any missing charges, atoms, bonds, nonbonding electrons, and curved arrows. Predict all the products of the reaction. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the structure, use the undo button on the lower left of the drawing canvas. Step 1: Add curved arrows. H H H : 0 | H 150 °C Step 2: Draw the products, including any lone pairs.
- ow the mechanism for the following reaction conducted at -5 °C in CC14: cyclohexene + bromine yields a dibromocyclohexane Draw structures - including charges and electrons - and add curved arrows. Details count. Step 1 Add three curved arrows to the first step. Draw the step 1 products: 1 organic species; 1 inorganic species. Step 2 • Reproduce the step 1 products. Add two curved arrows to show the bromide ion reacting with the organic species. Draw the final product. 1L o ↑ MapComplete the mechanism for the given reaction by adding the missing curved arrows. Step 1: Add curved arrows. Select Draw Templates More 2 → C G H → H H N CL Step 3: Add curved arrows. Select Draw Templates More Q2Q :0: ok Erase C H 0 N CL H a H Step 2: Add curved arrows. Select Draw Templates More G Erase Q2 Q (+ C H : 0: N CL Q2Q Final products Lor Erese H H :CI:2. Propose electron-pushing arrows for each step of the radical mechanism shown below. PhO,s.-so,Ph jor for > H [w-o [w-o Pho2s-sO,Ph H