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- 1 -Bromopropane on treatnent with alc KOH produces?Benzvl chloride can be converted into benzaldehvde by treatment with nitromethane and base. The reaction involves initial conversion of nitromethane into its anion, followed by SN2 reaction of the anion with benzyl chloride and subsequent Ε2 reaction. Write the mechanism in detail, using curved arrows to indicate the electron flow in each step.What 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 ОН
- No2 OH HNO3 HzSoy (Prolunt Prolct B 1) a) Draw fesenaree of materials. which Sing (esonance forms Icad to cach of the Predcts (A cnd B) b) Draw mechanisms to Form A and B Producks.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…of 42 > Macmillan Learning F3 Draw the product or products of the reaction. Include charges where appropriate. H3C OL $ H₂ 4 i CH3 CH DII % 5 8 FS NH₂ C + HCI F6 6 * F7 & 18 7 PrtScn Resources J FB Draw the product(s). Draw condensed hydrogens. Select Draw Rings More ★ $ / |||||| C H N CI 8 Ć Give Up? Home F9 ( 9 End Hint F10 O Q2Q 4 e PgUp 0 G F11 Check A Erase PgDn P 1 10/2 F12
- V. @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.Identify compound P, Q, R and S in the following reactions: OH C, H,0 D. Sebatian P Compound P CH3COC Sebatian Q Compound Q AIC, b) OH 1. LIAIH, THF Sebatian R Compound R 2. H30* Sebatian S Compound S d)k Draw the major product of this reaction. Include any relevant stereochemistry. Ignore inorganic byproducts. Qu EtO- EtO O= OEt NaH Problem 341 of 25 Drawing Atoms, Bonds and Rings Draw or tap a new bo
- Draw the mechanism ffrom benzaldehyde to this using: i)NaBH4 ii)TsCl, py iii)NaCN iiii)H+, H2OGve the major product of the followig reaction. H'oH heat HO. HO. OH LI There eno reactin under th contia recorct.produWhich product(s) will form under the conditions below? Br. -8308 deuterium bromide O A only O B only O Conly O Donly O A and D only OB and C only OA and Conly OB and D only OA, B, C and D Br A D Br
