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Q: 1. Draw the MAJOR products A - E for the following reactions. i. KMNO4, HO", heat SOCI, A В ii. H;O°…
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Using the nomenclature guidelines given in class, give the correct IUPAC names for the following compounds:
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- In each of the followinq rea ctions, t he indlicated procluct is either obtained poor yretd all. Provide the case, or not at detai led explanat con why this is a U ##f0d CH, (CO, Et),ci Ne GEt, EEOH PHCH(co U Ph Br CH2 CHO + CH, Č CH2 NADEE, CHz CH CH, C CHz Et OH NaOEE () CH2 CHO t CHq Ć CHzV. @Given the following reaction show the detailed mechanism fer me 1 Conversion of A tu B •OCN3 OYOCH'S (A) Na och 3 CH3OH. almost the Ⓒ detailed using the identical. cyclonexare ving as a structure and .d. cyclopentane ning instead (B) OH а mechanism, instead of shoaln in product B, propase mechanism fer a product W/ a cyclohexane ving.us not ev om ← Draw the major product of this reaction. Ignore inorganic byproducts and the carboxylic acid side product. O CH3OH (1 equiv) pyridine Drawing a Problem 211 of 34 Atoms, Bonds and Rings Charg OH о || S CI
- What is the likely product of the reaction shown? لیلی OH 01 0 || O ||| CO IV OV 1 excess NaBHA/CHJOH IV 11 OH OH OH OH ملیٹی میشی مسكن III OHWhat is the expected major product of the following reaction? H;SO.(aq) So,H SOH D. OB. B O D:D OE EA) Draw the prodocts of the folowing reactions taking into ccount the given moleciar formukas: HO NAOH CaH Br Ho NOOH 1B Why dipperent products are dbtained in te above reactions? 1C. 2- metnoxyethanol is a Sobstance Osed to meit ice and Snow..which reagent make it from epoxide? Draw a detailed mechonism, induding a hall - electron transition and intermediate Can be Used to products f the reaction.
- 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…9. Draw the constitutional isomer formed when the following alkenes are treated with each set of reagents: [1] H20, H2SO4; or [2] BH3 followed by H2O2, "OH. A io onutouTC.rvinmmoo ewo ebyoleen.g er besibhoyn motis M doso al waH s b. a. Seblaar molsHsno isq onol nose 2eob isticho to eqyt ewni.d Cnistnoo ennug 29ob anodogle yoam woH.o O bns 18 to alnemala erlT nertw bemot witam-S ae doue anexie leohtemmyeniGve the major product of the followig reaction. H'oH heat HO. HO. OH LI There eno reactin under th contia recorct.produ