Draw the major organic product(s) generated in the reaction below. Pay particular attention to regio- and stereochemical detail. H H CH3CO3H H₂CH₂C CH₂CH3 Draw the molecule on the canvas by choosing buttons from the Tools (for hondel Atome and Advanced Template
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- H₂C H H₁C Br NBS CH, CH₂ CC, hv **You may assume that Br-Br is formed by a side reaction that occurs (which we discussed in class). This is useful for one of the steps of the mechanism.What is the Potential energy diagram for this reaction. Pls draw with as much detail as possible. labels and scale) 2-methylpropan-2-ol ---> 2-methylpropene +H2O Draw the potential energy diagram for the reaction of 2-methylpropan-2-ol ---> 2-methylpropene + H20 (1) Label the structures of the (a) reactants, (b) intermediates, (c) transition states, (d) products, and (e) activation energies (E.) for each step. (2) Which step is the rate-determining step? (3) Identify the electrophile and nucleophile in each step when applicable.Complete the mechanism for the given base-catalyzed formation of a hemiacetal from cyclopentanecarbaldehyde and sodium methoxide in methanol by adding any missing atoms, bonds, charges, nonbonding electrons, and curved arrows. Step 1: complete the structure and add Step 2: complete the structure and add curved arrows. curved arrows. Select Draw Rings More Erase Select Draw Rings More Erase C H C H H. 1L :o - I :o :
- TROVIOW Topicaj (References) Draw the major organic product of the reaction shown below. HO, NANH2 You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Include cationic counter-ions, e.g., Na" in your answer, but draw them in their own sketcher. (Review Top Draw the major organic product of the reaction shown below. OH K2Cr207 H2SO4, H20 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one.2. Draw the expected major product if you used hydrobromic acid instead of phosphoric acid in the reaction and upload it here. Browse your files to upload or Drag and Drop Max attachments: 10 | Max Size: 20.00MB eachAdd any remaining curved arrow(s) to draw step 1 of one of the mechanisms. Modify the given drawing of the product as needed to show the intermediate that is formed in this step. Use the +/- tools to add/remove charges, and use the single bond tool to interconvert between double and single bonds. CH3 CH3 H;C, H,C CH3 CH3 ČH3 ČH3 + Edit Drawing
- Would these be the correct mechanism arrows for this reaction?13 Draw the complete arrow pushing mechanism for the following reaction. Indicate the Lewis acid and Lewis base (LA or LB) and whether they are also Bronsted acids and bases (BA or BB) for each intermolecular reaction. Add nonbonding electrons as necessary. Draw all the important resonance structure of the intermediates. You can use abreviated +H+/-H* notation. To preview image Click Here NH3 NH TSOH (cat.)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 +
- Draw th jor substitution products you would expect for the reaction shown below. If substitution would not occur at a significant rate under these conditions, check the box underneath the drawing area instead. Be sure you use wedge and dash bonds where necessary, for example to distinguish between major products. Note for advanced students: you can assume that the reaction mixture is heated mildly, somewhat above room temperature, but strong heat or reflux is not used. ***** Camil С HO :0 + X Click and drag to start drawing a structure. E ak 15a) Give a detailed (arrow pushing) mechanism for the following reaction, where appropriate label the Lewis/Bronsted Acids/bases b) On the provided axes, draw a reaction energy diagram for the reaction above, indicate the rate determining step and its activation energy, indicate the positions of any transition states and draw structures for all transition states. To preview the image click here HBr + CCl4 (solvent) Br2) Provide a detailed mechanism for the addition reaction shown below. State the regiochemistry and explain why it's unusual. Please be sure to include all structures (use line angle notation or perspective diagrams as appropriate to illustrate the stereochemistry of the process), resonance forms, intermkediates, transition states, curved arrows, formal charges, or lone pairs as necessary. Please don't cheat. Br HBr SCH3 SCH + EN