CUse curved arrows to show the mechanism of the step below. Make the ends of your arrows specify the origin and destination of reorganizing electrons. Arrow-pushing Instructions H3C. :0-H C: NH H-O:
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- Draw the complete mechanism for the reaction below. Make sure your mechanism meets the criteria listed here: There are 6 steps in the mechanism You must draw all curved arrows needed to show the movement of electrons The reaction is acid catalyzed, you will need to use the H3O+ in your steps Include all lone pairs and formal chargesPart A (1 of 1) Draw the curved arrows for Step 2 of this mechanism. Arrow-pushing Instructions n ņ H3C H3C C H :010 C. XT Mg. CIH Br CH3 CH3 H Step 2 H3C. H3C o: H 02. CII!!. C с CH3 Mg-Br エー CH3 HGive detailed mechanism Solution with explanation needed of each step....don't give Handwritten answer...
- 5d. (- the product, including cis/trans stereochemistry. If you know about rearrangements, apply your knowledge. If you don't, or are not sure, write that and ignore Show the El mechanism for the following reaction. Use your work to predict rearrangements. AHow can I approach this mechanism? This is what I have so far...Add any remaining curved arrow(s) to draw the last step of the mechanism. ODC 1Z+ D :0 CH3 CH₂ + CH3 & d d H с N O P S F LL CI Br I L Gl
- x. The oxidation shown below. PCC = CI-Cr-O: H-N But for the mechanism you can use chromic acid = HO-Cr-OH РСС OH Dry CH2CI2Show the electron-flow mechanism of the following. This involves predicting major and by-products using electronic and structural effect CH3 CI. `AI C=c-H H-CI 1 %3D + + + H H. CI Br CH3 + N-Br + Br-Br = CH3 12 Br CH3 CH2 + HBr %3D 3. || I IShow the curved-arrow mechanism for the first step, and the structure of the cyclic intermediate formed, when cyclopentene in treated with KMnO4 . A Lewis structure for the permanganate ion is provided in the hint. Make sure to show all non‑bonding electron pairs and formal charges where necessary. Omit K+ .
- 6.Q20. Please help me choose!A 1.62 M solution of (R)-2-butanol is mixed with an equal volume of a 0.810 M solution of racemic 2-butanol, and the resulting solution is analyzed in a sample container that is 1 dm long. What observed rotation is expected? The specific rotation of (R)-2-butanol is –13.9 degrees mL g- dm-'. a = deg

