Show the synthesis from acetylene for K (C11 H14 O) and O (C5 H12 O) using the spectra below
Show the synthesis from acetylene for K (C11 H14 O) and O (C5 H12 O) using the spectra below Molecule 1 Molecule O Mol...
Use the spectra below to answer for K and O Show the synthesis of Kt o from acetylene. PAFT I SYNTHESIS син o С, но . Molecule K 5H 2H diastereotopic - 1H PPM Molecule o 6H 4H 1H 1Н exchangeable PPM
Use the spectra above to determine the reactions and the products of K, and O Answer in the boxes below Reactions Products Syaimin tg Kio fmи аеyene adyene РАРТ Show Yu SprTHEGNS CuHMO CsHO Molecule K ЗН 3H 5H 2H diastereotopic 1н PPM o Molecule O 6H 4H 1H 1H exchangeable PPM K O К O
Use the spectra below to fill in the boxes for the reaction above. If it isn't clear box J is (C11 H24 O) and box I is (C9 H10 O) NARCC H240) NMR (Cq HOO) Molecule 9H Зн 2н 2н PPM Molecule ) 9H ЗН ін 2H 2H Е -
Use the spectra below to fill in all the letter spaces in the Guided synthesis Molecule 9H Зн 2н 2н PPM Molecule ) 9H ЗН ін 2H 2H Е - Molecule F IH L6H 2H2H Clotis 1. Imole Hel 1.Li/NH3 -78°c 2. Mc PBA 2. 1 mole HI Kamaryu H NMR/IR VE c) H₂O FNne) (NMR/IR lCq H180 co ter) C10Hz, Br
Below is the H NMR spectra for the molecule styrene. Consider if a hydroboration reaction was preformed on styrene. How would the H NMR of the expected product change in comparison to styrene? Circle which peaks from the styrene spectra would disappear and not be present in the NMR of the product. Draw the expected product. Describe the splitting pattern of each new proton signal that would appear in the NMR of the product. 2) Below is the 'H NMR...
Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For 1 H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a “zoom-in” on an important part of the spectrum. Mass Spectrum (not shown): [M] = 169 (100%) m/z IR Spectrum (not shown): 2985,...
NEED HELP WITH B) C) D) E) F) and G) that apply to the spectra below. OTHER ANSWERS ARE THERE TO SUPPLEMENT Thank you! 5. Using the GC mentioned in question 4 and the values listed on the chromatogram for the height and width (at half height) of each peak, calculate the percent composition for each product (A, B and C). Be sure to show your work. Area of peak A = 125 x 8 = 1000mm2 Area of peak...
Unknown H415 100 50 1000 1S00 2000 3000 BRVENUMBERI 4000 Unknown H415 ЗН 1 H-N 2H, q 1H, d 5H, m 1H, d 0 1 2 3 6 7 8 10 11 ppm HSP-00-049 Unknown H415 q 140 120 100 200 180 160 ppm CDS-00-726 20 -40 60 80 Relative Intensity 09 Unknown H415 100 MS-NJ-0442 80 20 thmpt 25 50 75 100 125 150 175 m/z Date: Name: Section/Group: Instructor: Report Sheet: Laboratory 14 MS,IR, 13C NMR, and 'H...