Mass Spectrum 24 700 100 110 120 139 140 150 16O 170 18O 190 200 90 mie Infrared Spectrum Wave Number, cm 4000 000 2500 2000 IS0 1300 1200 1100 700 12 13 14 15 'H NMR Wavelongth, microns Strecture "C Spectral Data: doublet, 80.4 ppm singlet, 68.3 ppm triplet, 14pn 50.0m 02000 Brooks Cole Publishing Company Ausuasu aouequosay
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- Add Ink to Ink to Drawing Canvas Pen Shape Math Comvert Insert CHICHOBENICOCE 2 3C S 13 15 16 (Complete the mind map given Observation: veddish brown of Brs deolounzed -Br Br CH,CI, Br2, H20 Cl2, CIA HBr H;C H,O, H,o H2, Pt conc. H,SO, H2C CH CHS он dilute KMno . OH- heat 4+ CH2 CH2 HCI + mn Oz HCI, H,O Her, CH,0OCH, observation: purple cSlour Br, CI, Cl,, H,O dikúte H, So, 5 yvees ENG US11. Order each set of compounds with respect to Sy1 reactivity. (1=lowest, 3=highest) а) H,C CH3 NH2 H3C-C-CI 'CI CH,CH,CHCH3 b) (CH3)3CF (CH3),CBr (CH3),COH c) CH, CH,Br CHBR Br13:34 all 4G O. What is the final product(s) of the following reaction? CH,OH [H,SO,) OA OH H,CO OB. OH но H,CO OCH major minor Oc но OCH D.None of the above Add a caption... > Status (Custom) +
- Draw the structures of the starting material and the four missing intermediates. он H2O2, H2SO4, MeOH allyl bromide, K½CO3 acetone, reflux (97%) MeO OMe (99%) ÒMe Оз. Осм, МеОн, -78°С then Me,s DMF, 190 °C BnBr, K2CO3 acetone (99%) (93%) (78%) Br OBn NBS, DCM (95%) Meo OMe ÓMehelp with the following ochem question part a, b, and c regarding the NMR for the compound.... (5S, 7R)-7-bromo-,3,9-diethyl-6,6-dimethylundec-3,8-dien-5-olWhat is likely true for the first step in this mechanism? :OH ○AHO ○△H > 0 ○△HO H-Br: H Br H. H2O 王茄子一人 :Br: More information is needed to decide
- What step(s) will achieve the desired conversion of the SM to the P? A. 1. NaOMe, MeOH; 2. HIO4, 1,4-dioxane B. 1. H3O, H₂O; 2. HIO4, 1,4-dioxane C. O3 (g), CH2Cl2; then PPh3 D. Dess-Martin Periodinane SM Conditions x-12. Order each set of compounds with respect to S,2 reactivity. (1=lowest, 3=highest) a) CH3 H,C--CI CH,CH,CH2CI CH,CH,CHCH3 b) Br Br Br c) Br4) Complete given reactions. (They have missing parts) Categorize them accerding to their forbidden degrees and write their type of passing (0*) > 42 22 -> 49 50 Hel ) 3 3 c) -> 2 76 76 Se lo7) -> 34 (P 35
- Draw the organic and inorganic products of the reaction, describe the type of bond cleavage, and classify the reaction. 80 : Br R F -CH₂-CH3 + 0-H Identify the type of bond cleavage: V 888 F4 5 T G B 6 MacBook Pro Y FO H & 7 N JA F7 U J Draw the products, including hydrogen atoms, charges, and nonbonding electrons. Select 3 Ć * 8 M DII FB | Draw Rings More ( 9 K DD F9 O < H ) O. L F10 command P . V Q2Q F11 I { + [ option = F12 11 Erase 1 del2) Write the major products A- P for each of the following reactions. (70 point) HBr CH,CH,OK* CH;CH,OH t-BuO'K a) Br t-BUOH Br,/ H20 F Br KMNO/ OH Zn 1) 0, 2) Zn/ CH;COOH b) Br NANH, CH,CH,I H. Li NH; -78°C d) A concd. H,SO, L. H,O/ H Br, CCl, excess NaNH, hear NH,1. Which of the following compound will show two absorption bands at around 2700 cm³¹ and around 2800 cm¹ along with the carbonyl absorption [Select] 4 Click here to preview the image B :0: A A CO :0: lg i l N B C 2. Which of the following compound will show absorption band ~3300 cm¹ [Select] Click here to preview image A B B D C H 3. Which the following compound will show absorption band ~1735 cm1 [Select] Click here to preview image e D NH