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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- 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 NA XII myhot H3C. HC Use 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 H2ö* N(CH3)2uestion 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 *3
- HO: What is wrong with the mechanism described below?V Add one curved arrow to draw the next step of the mechanism. Modify the given drawing of the product as needed to show the intermediate that is formed in this step (a sigma complex). Use the +/- tools to add/remove charges, and use the single bond tool to interconvert between double and single bonds. IN Z + + + +1 02CX e o soặc CH3 Ö: CH3 1 H Z O C P S F CI BrPart A (1 of 2) Draw the curved arrows for Step 4 of this mechanism. Arrow-pushing Instructions CH3 H. CH3 Н. :Br: Step 4 :N N=c=ö: Next (1 of 2) Recheck 3rd attempt Incorrect Double-headed arrows denote the movement of a pair of electrons, so an arrow must start from either a bond or a lone pair. There are 3 arrows in this step.
- MECHANISM ACTIVITY Base-Induced Ester Hydrolysis (Saponification) NOC XT Step 1: Nucleophilic addition of hydroxide ion to the ester carbonyl group Ahrs MPR R16 H3C. R Part A (1 of 2) Draw the curved arrows for Step 1 of this mechanism. Arrow-pushing Instructions CH3 H-O: ÖH OR' :Ö H-O: O: H H H H 1x xxx CH3 CH3 Step 1 H3C. CH3 заkindly answer from C to EH но. но HO Ethylene oxide is the starting material for the synthesis of 1,4-dioxepane. Draw curved arrows to show the movement ofelectrons in this step of the reaction mechanism. Arrow-pushing Instractions HO+ но H,ö: HO: :o: :o: I-
- CH₂CH3 H3C-C-CH3 Br: ṇC↔X™ H ;0: H3C Check + For the reaction above, draw curved arrows to show the movement of electrons in the step of the mechanism shown below. Arrow-pushing Instructions + 30: Next (1 of 1) H3C CH3OH CHCH3 H3C-C-CH3 H CHCH3 H3C-C-CH3 fast H BO-H + H3C CHCH3 || H3C-C-CH3 Previous NextThe following figure shows the energy profile of a nucleophilic substitution reaction. Potential energy :ÖH H HII.C H C-1 H HO--C---I HH Reaction coordinate H -CH HO–CHITH H + 1 According to this, it is correct to affirm: O The activation energy (4G°) shows that it is thermodynamically favorable. O Represents a reaction that occurs in one step where a pentavalent chemical species is formed. O The intermediate has lower energy than any transition state. O The formation of the intermediate releases energy and is therefore thermodynamically favourable.b For the mechanism step below, draw curved arrows to show electron reorganization. Arrow-pushing Instructions :0: -N-N=N: :CI: