H,Cro SOCI: H,0 Pyridine PCC CH,CI, HIO HR Peroxide 2. H,0,HCI NES CH- - HN CH,I,...
Show each step 1. PPh; 2. Buli 0 3 он 1. PCC, CH,CI, ,H,O+ 1. 9-BBN 2. H,O, OH- 3. (2) EtOH, H2O+ 1. MeCI, AICI: 2. NBS, hv 3. NaOH 4.PCC, CH,CI, 5. KCN, HCN
33. What is the product for the following sequence of 1. Acetylchloride, AICI, 2. Zn(Hg), HCI reactions? Practice Which is the major isolated organic product after this series of steps? 1. LDA 2. EIB 3. M,0". Bry 3. NBS 4. PPhy 5. n-Buli 6. acetone 7. m-CPBA B. C. D. D. E. What is the reactant for the following sequence of reactions? 1. NOEI 2. HA OH 3. H,O heat 5. LDA & EB 7. NAH, OH & olyang 315...
thanks! On each the following IR spectra, circle and indicate the most important stretching signal from the following choices:N-H, O-H, CEN, CEO, C-O, Top, IR spectrum of Compound 18a: C14H1402 Bottom, IR Spectrum of Compound 18b: C3H120. write your answer on the corresponding square provided (2.5 pts each, 5 pts total) mar 2000 6 C-OR Characteristic IR Stretching Frequencies in cm broad N-H 0-H CEN (3000-3500) (2200-2400) 4000 3000 2000 (1150-1300) 요 RC-O (1600-1750) (1250-1350) (1050-1150) 1500 1000 500 'H-NMR...
Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Propose an efficient synthesis for the transformation below, using two sequential reductive aminations. Enter the appropriate number or letter from the reagent list handout. Step 1 + NaBH3CN, H+, Step 2 - NaBH3CN, H+ Reagent List (Updated 4/30/2020) Enter # or letter in the appropriate boxes. Note: Exam responses are case insensitive Alkyl Halides (X = Cl,...
thanks! For compound 18a the signal "e" is not 2H it is 3H, this was a typo 18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of each compound (4 pts) (30 points total) Unsat. Index = (2C+2-H-X +N)/2 = 3.0 2.00 25 490 2.0 e = 2.00 ppm. singlet, 2H d = 2.66 ppm, quartet, 2H f = 1.27 ppm, triplet, 3H 720...
thanks!! There is a mistake on this, e on compound 18a is 3 hydrogens not 2!!!! thanks again :) On each the following IR spectra, circle and indicate the most important stretching signal from the following choices:N-H, O-H, CEN, CEO, C-O, Top, IR spectrum of Compound 18a: C14H1402 Bottom, IR Spectrum of Compound 18b: C3H120. write your answer on the corresponding square provided (2.5 pts each, 5 pts total) mar 2000 6 18. Draw the structures of Compound 18a. and...
Thanks! On each the following IR spectra, circle and indicate the most important stretching signal from the following choices:N-H, O-H, CEN, CEO, C-O, Top, IR spectrum of Compound 18a: C14H1402 Bottom, IR Spectrum of Compound 18b: C3H120. write your answer on the corresponding square provided (2.5 pts each, 5 pts total) mar 2000 6 18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of each compound (4 pts) (30 points total) 30 Unsat. Index = (2C+2-H-X+NY2 = 200 25 e = 2.00 ppm, 4.90 f = 1.27 ppm, 20 720 Compound 18a: C,H,O, singlet, 2H triplet, 3H 127 15 d = 2.66 ppm, a = 7.21 ppm, b = 7.18 ppm, doublet, 2H doublet, 2H C = 4.90...