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- Predict the product of the reaction shown and complete the curved-arrow mechanism for its formation. (Hint: Friedal- Crafts alkylations can be used to form rings.) AICI, → a compound C,H2 + HCI PHCH,CH,CH,CH,CI- Step 1: Draw one curved arrow. Step 2: Complete the structure, then draw curved arrows for the EAS reaction. Select Draw Rings More Erase Select DrawRings More Erase H Al Cl H Al Cl : C : Al : d :The following reaction mechanism contains mistakes. Which of the following statements correctly describes how the first curved arrows should be drawn? OO | || CH3CH₂CH₂O-H +Na NH3 ||| IV + CH3CH₂CH₂0 Na A. The curved arrow should start at sodium ion labeled (1) B. The curved arrow should start at the hydrogen atom labeled (II) + ⒸC. The curved arrow should end at the bond between the oxygen atom () and the hydrogen atom (II) D. The curved arrow should start at the lone pair of electrons on the nitrogen atom labeled (IV) E. There should be an arrow from the oxygen atom (1) to the hydrogen atom (II) NH3Write down major r producto), or other recietent6) and/or fallawine the reactionconditions for the Ht Na BH (OAC)S +(CH2)2NH 1. CH3 CH2 Mg Br 2. H30+ CH2CN CH30 OEt 1.NaOH, tho A 2. H3ot 3. A
- Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the product of this elementary step in an E1 mechanism. Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore byproducts. H₂ 0.01 M NaOH heat H < (+ Na OH Atoms, Bonds and Rings Charges and Lone Pairs Draw or tap a new bond to see suggestions. Undo Reset Remove Done Drag To Pan +Can you draw the products that form when 1-butene reacts with; O3, then Me2S OsO4, then NaHSO3/H2O Br2 in H2O Please analyze in detail for each. Also can you please reply fastly?Draw the missing reactants/ intermediates in this E1 mechanism. Include all lone pairs. Ignore byproducts.lgnore stereochemistry. H,0* :OH Drawing dissociatio n 1,2-hydride shift i Select to Draw Inter mediate Atoms, Bonds and Rings Charges and Lone Pairs elimination Draw or tap a new bond to see smart suggestions. Undo Reset Remove Done Select to Draw
- uestion 8 of 8 Step 2 Draw step 2 of the mechanism. OりCX 0 @ H + H,C CI Br .. MacBook Air 吕口 888 F5 F7 FB F10 23 2$ 4 & 2 3 5 7 8 9 W E R. T Y D F K T Z +| +† +t +l *3Substitution and elimination: predict the product Maximum allowed tries per question: Unlimited (7) Draw the major organic product of the reaction. Follow this procedure: determine whether the reaction conditions are acidic or basic; identify the most nucleophilic/basic atom, the electrophilic atom, and the leaving group; predict whether elimination or substitution will occur; and then draw the product. Indicate the stereochemistry at every stereocenter with a single wedged (up), hashed (down), or wavy (a mixture of up and down; either) bond. Launch MarvinJSTM viewer or click image to copy source CH3 H3C EtONa EtOH Brс-НCI (1 drop) H. OCH2CH3 H2N NH2 O2N ethanol, reflux 1. major product 2. the most plausible mechanism plz
- 2. Label the following reactions as most likely occuring by an SN1 or SN2 mechanism. Explain your answer. (4 marks) HBr A) HO, CH;CH2OH 'Br B) Na* SCH; CH;CN ‚Br „SCH3Substitution and elimination: predict the product Maximum allowed tries per question: Unlimited (5) Draw the major organic product of the reaction. Follow this procedure: determine whether the reaction conditions are acidic or basic; identify the most nucleophilic/basic atom, the electrophilic atom, and the leaving group; predict whether elimination or substitution will occur; and then draw the product. Indicate the stereochemistry at every stereocenter with a single wedged (up), hashed (down), or wavy (a mixture of up and down; either) bond. Launch MarvinJSTM viewer or click image to copy source CI benzene Aoctane + NOx + hv (assume hydrogen on second carbon bonded the weakest) For each mechanism, provide the photolytic cycle, a source for hydroxyl radical (if needed) AND atermination step. You may stop when you have accounted for all radicals AND all VOCs are stable (i.e., ifformaldehyde is a product of your mechanism, you do not have to oxidize that molecule to).