Pre-Lab Q1 Homework Unanswered Due Today, 4:00 PM Predict the product of the following reaction. H3C OME OMe OH OH H3C CH3 1,3-pentanediol catalytic OH Ole Me (p-TsOH) OMe CH3CN benzaldehyde dimethylacetal H. MeO OMe OMe McO OMe HOOCH3 CH3 H3C CH3 H3C CH3 H3C CH3 E D C O Targets placed: 0/1 You can place up to 1 targets Unda Delete selected Remove All
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- O Complete the following chemical reaction catalyst b| H3C w CHz t HzO ) HgC a CHs + He Pd/Cy H3C ~CH3 t Br-Br e) ce 8 Chlorination of ethane under ultraviolet light 9 hydlogenation of buta-lyne with a phtinum catalyst.5- 4- 1. CH3CH₂MgBr Br 2. H₂O Mg/ether 1. iH 2. H₂O← Aktiv Chemist X → C 43 F Mostly cloudy UL Week 7: Panc X app.101edu.co FI Draw an alkyl halide and choose the best reaction conditions that would undergo an SN2 reaction to yield this product shown below. @ 2 F2 UL LTU 7-1A X Drawing # 3 DII -N=N= F3 C|Chegg.com X $ 4 N 4x H F4 % 5 J C|Chegg.com x F5 Question 2 of 24 A 6 C|Chegg.com x Atoms, Bonds and Rings. F6 Draw or tap a new bond to see suggestions. & 7 G Draw the pro X F7 Charges PrtScn ★ 8 FB C Draw the pro X Home ( 9 F9 A End ) 0 + ← Undo F10 To S Ⓒ Remove Done ENG II Reset PgUp 40) O Sub Drag 10 P
- 10 ll atit VPN * +964 771 368 9066 قبل ۲۰ دقيقة rcise 23-6 it Yourself ormulate a mechanism for the following reaction. 1. CH,CH-O-Na*, CH,CH OH 2. H, HO co.CH,CH3 + CH,CO,CH,CH3 -Co.CH,CH, COOCH2CH3 Diethyl 1,2-benzenedicarboxylate (Diethyl phthalate) 60-80%Predict the products for the following reactions by showing complete reaction mechanisms. Also, identify the nucleophilic attack, loss of leaving group, proton transfer, rearrangement in the mechanism steps. Show curved arrows in the reaction mechanisms 1- 2- COCH3 NaBH4/H₂O COCH 3 1. LIAIH4 2. H₂OCould u show the products and the mechanism of the following reaction and give a short explenation? Is it possibel for elemental bromine to form ? CH KBRO3 + HBraq. H3C НОАС P. +
- 10. Propose a mechanism for the benzoin condensation, which is specifically catalyzed by cya- nide: () 2Ar-C-H CH₂-C-CH₂-C-H CN O OH Ar-C-C-Ar H 11. Propose a mechanism for the following transformation: COOC H. Nall COOC₂H₂ H₂C-CH-PPh,Br H₂C coỌC H COOCH, + Phụ P=0dedcue the major organic product from the following reations. be ablw to draw hydration halogenation hydrohalogenation, halohydrin formation, oxymercuratiom demercuration qnd hydroboration oxidation.Can you please draw out a complete curve arrow mechanism with the reagent and intermediate steps?