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- 4) Eto ₂ 5) 2-Cyclohexene-1-one O₂Et + ethylace to acetate NaOEt NaOEtClear my choice Which of the following is/are the expected product/s of the reaction of 2-pentanone (CH3COCH CHACH) with excess Bro, followed by OHT? O CHCOCHBRCH,CH3 BICH,COCH2CH;CHa O CHBr + CH,CH,CH,COO OCHBR + CH,CH,CH,COOH Which compound can undergo Cannizzaro reaction? CH,CHOIn the reaction between 1-methylcyclohexanol with hydrogen bromide to form 1-bromo- 1-methylcyclohexane and water, a) How would the rate be affected if the concentration of HBr is doubled? pls. draw involved reactions
- 5) Complete the following reactions a) cH3- CHz COOH + b) cH3 - CHz CooHt LioH - c) CH3 COOH + Hg CO3What is the predicted product of the reaction shown? ОТ O II O ||| O IV OV Н Na2Cr2O7/H2SO4/H2O IV || ОН ОН овог H V Ш OH ОНWrite the complete stepwise mechanism for the reaction below: (Non-anonymous question (Ⓒ) OH HC1 OCH3 CH3OH H₂O C
- Which of the following reactions will not generate an alcohol group in the product? (1) CH,CH;MgBr Reaction A (2) dil. H* /H;O NaOH Br Reaction B H2O//THF (1) Hg(OAc)/ H0 Reaction C (2) NABH/ethanol NAOH Reaction D H2O//THF OReaction B Reaction A Reaction C Reaction Do OH 3) Please draw the structures that correspond to omitted structure for each of the following synthetic sequences. HO Cro3 Cl (d) Cro3 (a) Product `OH Product OH H30 H30 HO PCC Cl PCC (b) Product (e) `OH Product "OH HO РСС NABH4 (f) Starting Material Product 'OH ELOH6-46 Show how each compound might be synthesized by the SN2 displacement of an alkyl halide. SCH,CH, (a) -CH₂OH (c) (d) CHÍNH, 6-47 (a) Give twn synthecac fox (CI) qu (b) (e) H₂C=CH-CH₂CN n OLL BU (1) H-C=C-CH₂CH₂CH₂
- Name: 13Vicopo wug Speucy Subject: 1. Name the following alkyl halides: 1a Course and Year: ahotaewio P lo SCORE: ont Ta LGRILICICg co combonuga cou eq to (a) H3C Br Br CH3 nodo (b) (c)od Br CI CH3 CH3CHCHCHCH2CHCH3 I eq CH3CH CHCH2CHCH3 onb pougcg to s Aac ebspapiqscq CH3CCH2CHCHCH3 CH3 CH2BR (e) CICH2CH2CH2C=CCH2Br (p) CH3CH2CHCH2CH2CH3 2. Draw structures corresponding to the following IUPAC names: obiw 0 alordoolA lonarisM 2noiisoilqqs OL SIT (a) 2,3-Dichloro-4-methylhexane s (b) 4-Bromo-4-ethyl-2-methylhexanema sug una csmc ro pe cCSTIcg moog aicouo 13 (d) cis-1-Bromo-2-ethylcyclopentane (c) 3-Iodo-2,2,4,4-tetramethylpentane M sob bnn CE 3. How would you prepare the following compounds, starting with cyclopentene and s any other reagents needed?0 bos ouson brs (OgHO abrdablaot lo noloub01g CH (a) Chlorocyclopentane (b) Methylcyclopentane El (d) Cyclopentanol osinsmsh vd noitouboig to (c) 3-Bromocyclopentene nd asd 130 (e) Cyclopentylcyclopentane n noillim (f) 1,3-Cyclopentadiene un…V. @Given the following mechanism fer me Y OCHS NaOH reaction show the detailed conversion of A to B •OCN3 CH3OH. OH (A) (B) c Ⓒ using the same detailed mechanism instead of cyclonexare ring as shown in product. B, propose and fer a product wil a cyclopentane ning instead of a cyclohexane viny. Ⓒ Exploumpand I with why campand (B) is preferred over the campanay campand with a cyclopentake ring..What is the likley product of the reaction sequence shown? MgBr MgBr ОН РСС H2O K,Cr207/H2SO/H2O H,O CH2ČI2 ether ether ОН HO || II IV V O II O IV O v