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- 13518. IIIa) propose a reasonable mechanism/arrow pushing for the following reaction: R C 0-0 R N R Ruestion 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 *3Provide the mechanism EtNH3 EEN H₂ H H- ∙DH 3/ Et ·C=N "Fo OH Et 1 - NH H₂C ko
- Multiple step cross coupling reactions give me the synthesis step 8-8 요요 OEt HFor the SN 1 reaction, draw the major organic product, identify the nucleophile, substrate, and leaving group, and determine the rate limiting step. 20 R F V DOD H % 5 T G B Y H CH3CH₂OH (solvent) MacBook Pro F6 N & 7 U F7 J * 8 M DII F8 K Draw the major organic product. Select Draw Templates. More 9 / | || H F9 O L C H 0 F10 P A 23 Q2Q F11 command option 3 ? F12 EraseIn the mechanism for the nitration of benzene, what step follows the formation of the nitronium ion (NO2*)? benzene attacks the nitronium ion to give a sigma complex O benzene is protonated by nitric acid to give a sigma complex the sigma complex is deprotonated, thereby restoring aromaticity a leaving group is ejected, thereby restoring aromaticity
- 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 заPropose a plausible mechanism for the followng reaction INa, NH3 (liq) 2 NH CIPredict the organic product for the reaction. OH K₂Cr₂O7 H₂SO4 :ÖH acetone Select Draw Templates More H₂CrO4 |||||||CH 0 Add four curved arrows to complete the intermolecular mechanism that forms the oxidized product. Note that potassium dichromate in acid is in equilibrium with chromic acid used. 3 Select Draw Templates More H H 0: C H H Cr 0 : OH Q : 0:
- Draw Intermediate CH3OH₂+ protonation H H3C -0 H Q CH3OH deprotonation loss of H₂O elimination H3C :0 ÖH -CH3 Draw Intermediate CH3OH deprotonatio Please select a drawing or reag31. Which mechanism is correct for the following intramolecular substitution reaction? (a) (b) (c) 4- H-N H H N: H H₂N N: он --مرح CI CI CI H H CI N: NaOH N: CI *H :OH -- NH NH CNH на он NH NHPyridine reacts with hydroxide by nucleophilic aromatic substitution. Complete the mechanism by drawing curved arrows, the structure of the charged intermediate, and the structure of the major uncharged product. All non-bonding electrons must be shown, including those associated with charges. Step 1: Draw curved arrows. Select Draw Templates More ||||||||||| C H H 1 0: 3 C cl N 0 : a: Q2Q Step 3: Draw the uncharged product. Chloride ion is pre-drawn for your convenience. Select Draw Templates More ||||||||||| CH cl N O Erase : CI Erase Q2 Q Step 2: Draw the charged intermediate. Draw curved arrows to form the product. Select Draw Templates More ||||||||||| CH cl N G E 0 Erase Q2Q